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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04822480
Other study ID # 2020V0327
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date February 1, 2020
Est. completion date December 31, 2024

Study information

Verified date April 2024
Source University of Mississippi Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The National Diabetes Prevention Program (DPP) is an evidence-based, 12-month lifestyle change program to prevent or delay the onset of type 2 diabetes mellitus (herein referred to as 'diabetes') among adults with prediabetes. The Department of Preventive Medicine, University of Mississippi Medical Center (UMMC), in partnership with the American Medical Association, is collaborating to develop and implement the DPP as a clinical service for UMMC patients beginning in September 2020. We aim to recruit 245 patients per year over 3 years. Because this is the first attempt to develop and implement the DPP as a clinical service at the UMMC, we are proposing to conduct a comprehensive process, outcome, impact and return on investment evaluation. An effectiveness-implementation hybrid research design will be used to (1) evaluate a multifaceted implementation strategy and the effectiveness and impact of the DPP delivered using telehealth by UMMC's Department of Preventive Medicine; (2) conduct an analysis on medical expenditures among those who participate in a DPP to measure net savings and return on investment (ROI) relative to non-participants; (3) conduct a longitudinal cohort analysis to assess incidence of diabetes and changes in body composition, biomarkers, and psycho-social behavioral constructs among those who participate in a DPP relative to those who do not. The findings from this comprehensive research evaluation will be used to (1) improve clinical operations and implementation; (2) demonstrate the cost benefit of the DPP as a clinical service for patients with diabetes risk; and (3) provide empirical support for delivering the DPP via different modalities including telehealth to reduce risk and improve health outcomes among patients.


Description:

The purpose of this research is to: (1) Evaluate a multifaceted implementation strategy for the uptake of a remote DPP by UMMC's Department of Preventive Medicine. (2) Conduct an analysis on medical expenditures among those who participate in a DPP to measure net savings and ROI relative to non-participants. (3) Conduct a longitudinal cohort analysis to assess incidence of diabetes, body composition, biomarkers, and psycho-social behavioral constructs among those who participate in a DPP relative to those who do not. Study methods are described below according to each of three specific aims. Aim 1: Conduct a concurrent implementation and effectiveness evaluation of the DPP in a clinical care setting for patients with prediabetes (n=245). An effectiveness-implementation hybrid type III research design will be used to conduct a non-randomized trial with 245 of patients with prediabetes over a three year recruitment period, while employing an iterative process evaluation to explore the complex processes, dynamic context and organizational influences on implementation. The RE-AIM framework will guide the implementation and effectiveness evaluation including measures of Reach, Effectiveness, Adoption, Implementation and Maintenance. Multiple data sources and data types will be used to assess barriers and facilitators that affect the RE-AIM domains, as well as fidelity, costs, patient satisfaction and physician burnout. Aim 2: Utilize claims and encounters data to measure medical expenditures for patients with prediabetes, and determine spending differentials among DPP participants compared with non-DPP participants. Track trends in per capita medical expenditures for among a panel of case (DPP participant) and control (Non-DPP participant) subjects. To compare variations in spending, the differences in the arithmetic means, compound annual growth rates, and propensity score matching models will be implemented to compare case and control subjects. The study may also look at those with prediabetes that are later diagnosed with diabetes and individuals with prediabetes who are not later diagnosed with the condition. These estimates of spending differentials and evidence of DPP participation and engagement rates will help to further enhance the algorithm to estimate the potential cost savings and ROI if diabetes is prevented or delayed in the at-risk population who participate in the DPP. Aim 3: Assess the longitudinal effect of the DPP on participant changes in cardiovascular disease risk including anthropometric and clinical biomarker and psychosocial health outcomes (N=245). A prospective, repeated measures, experimental cohort design will be used to determine the long-term impact of the DPP on diabetes incidence and cardiovascular disease risk among DPP patient participants.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 500
Est. completion date December 31, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - UMMC patient within the previous 3-years (at least one UMMC clinical visit within the previous 3-years) - = 18 years AND - Clinical diagnosis for prediabetes (R73.03) OR any of the following combinations: - BMI =25 (non-Asian) OR - BMI =23 (Asian) AND - HbA1c 5.7 - 6.4 percent within the past 12-months OR - Fasting plasma glucose 110 - 125 mg/dL within the past 12-months OR - 2-hour plasma glucose 140 - 199 mg/dL within the past 12-months Exclusion Criteria: - Pregnant or planning to become pregnant within the next 12 months - <18 years - Primary or secondary diagnosis of diabetes mellitus (all codes with prefix of 250 and 249) and other conditions associated with diabetes (357.2, all codes with prefix 362, 366.41, and all codes with prefix 648). - End stage renal disease

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Diabetes Prevention Program (DPP)
Individuals with prediabetes can mitigate the risks and costs of diabetes by taking preventative action, such as participation in a National Diabetes Prevention Program (DPP). The DPP began as a multisite randomized controlled trial demonstrating the effectiveness and cost-benefit of a 12-month intensive lifestyle intervention over pharmaceutical treatment for preventing or delaying diabetes among prediabetic participants. In 2010, Congress authorized the Centers for Disease Control and Prevention to lead the dissemination of the DPP as a targeted approach (high risk populations) and population-based strategy to reduce the incidence of diabetes and diabetes-related healthcare costs. The goal is to achieve modest weight loss (7%) by developing and implementing behavior change skills resulting in lifestyle modifications such as physical activity (150 minutes per week) and dietary and nutritional practices.

Locations

Country Name City State
United States University of Mississippi Medical Center Jackson Mississippi

Sponsors (3)

Lead Sponsor Collaborator
University of Mississippi Medical Center American Medical Association, Mississippi State Department of Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 3-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 6-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 9-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 12-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 15-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 18-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 21-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 24-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 27-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 30-months
Other Eligible DPP patients (reach) Proportion of patients eligible for DPP relative to total number of patients in ambulatory setting; electronic health record Baseline to 33-months
Other Patients eligible for DPP (reach) Total number of patients in the ambulatory setting eligible for DPP; electronic health record Baseline to 36-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 3-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 6-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 9-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 12-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 15-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 18-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 21-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 24-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 27-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 30-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 33-months
Other Patients referred to DPP (reach) Total number of patients in the ambulatory setting referred to DPP; electronic health record Baseline to 36-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 3-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 6-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 9-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 12-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 15-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 18-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 21-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 24-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 27-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 30-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 33-months
Other Patients enrolled in DPP (reach) Total number of patients in the ambulatory setting enrolled in DPP; electronic health record Baseline to 36-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 3-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 6-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 9-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 12-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 15-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 18-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 21-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 24-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 27-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 30-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 33-months
Other Referring clinical sites (adoption) Total number of clinical sites referring patients to the DPP, electronic health record Baseline to 36-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 3-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 6-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 9-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 12-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 15-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 18-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 21-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 24-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 27-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 30-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 33-months
Other Referring providers (adoption) Total number of providers referring patients to the DPP; electronic health record Baseline to 36-months
Other Implementation Qualitative assessment of implementation processes Continuous processual evaluation
Primary Type 2 diabetes mellitus diagnosis Diabetes diagnosis extracted via electronic health record; all codes with prefix of 250 and 249 Change diabetes diagnosis from baseline to 6-months in DPP compared with non-DPP patients
Primary Type 2 diabetes mellitus diagnosis Diabetes diagnosis extracted via electronic health record; all codes with prefix of 250 and 249 Change diabetes diagnosis from baseline to 12-months in DPP compared with non-DPP patients
Primary Type 2 diabetes mellitus diagnosis Diabetes diagnosis extracted via electronic health record; all codes with prefix of 250 and 249 Change diabetes diagnosis from baseline to 18-months in DPP compared with non-DPP patients
Primary Type 2 diabetes mellitus diagnosis Diabetes diagnosis extracted via electronic health record; all codes with prefix of 250 and 249 Change diabetes diagnosis from baseline to 24-months in DPP compared with non-DPP patients
Primary Type 2 diabetes mellitus diagnosis Diabetes diagnosis extracted via electronic health record; all codes with prefix of 250 and 249 Change diabetes diagnosis from baseline to 30-months in DPP compared with non-DPP patients
Primary Type 2 diabetes mellitus diagnosis Diabetes diagnosis extracted via electronic health record; all codes with prefix of 250 and 249 Change diabetes diagnosis from baseline to 36-months in DPP compared with non-DPP patients
Primary Hemoglobin A1c Lab values extracted from electronic health record Change in HbA1c from baseline to 6-months in DPP compared with non-DPP patients
Primary Hemoglobin A1c Lab values extracted from electronic health record Change in HbA1c from baseline to 12-months in DPP compared with non-DPP patients
Primary Hemoglobin A1c Lab values extracted from electronic health record Change in HbA1c from baseline to 18-months in DPP compared with non-DPP patients
Primary Hemoglobin A1c Lab values extracted from electronic health record Change in HbA1c from baseline to 24-months in DPP compared with non-DPP patients
Primary Hemoglobin A1c Lab values extracted from electronic health record Change in HbA1c from baseline to 30-months in DPP compared with non-DPP patients
Primary Hemoglobin A1c Lab values extracted from electronic health record Change in HbA1c from baseline to 36-months in DPP compared with non-DPP patients
Primary Fasting plasma glucose Lab values extracted from electronic health record Change in fasting plasma glucose from baseline to 6-months in DPP compared with non-DPP patients
Primary Fasting plasma glucose Lab values extracted from electronic health record Change in fasting plasma glucose from baseline to 12-months in DPP compared with non-DPP patients
Primary Fasting plasma glucose Lab values extracted from electronic health record Change in fasting plasma glucose from baseline to 18-months in DPP compared with non-DPP patients
Primary Fasting plasma glucose Lab values extracted from electronic health record Change in fasting plasma glucose from baseline to 24-months in DPP compared with non-DPP patients
Primary Fasting plasma glucose Lab values extracted from electronic health record Change in fasting plasma glucose from baseline to 30-months in DPP compared with non-DPP patients
Primary Fasting plasma glucose Lab values extracted from electronic health record Change in fasting plasma glucose from baseline to 36-months in DPP compared with non-DPP patients
Primary 2-hour plasma glucose Lab values extracted from electronic health record Change in 2-hour plasma glucose from baseline to 6-months in DPP compared with non-DPP patients
Primary 2-hour plasma glucose Lab values extracted from electronic health record Change in 2-hour plasma glucose from baseline to 12-months in DPP compared with non-DPP patients
Primary 2-hour plasma glucose Lab values extracted from electronic health record Change in 2-hour plasma glucose from baseline to 18-months in DPP compared with non-DPP patients
Primary 2-hour plasma glucose Lab values extracted from electronic health record Change in 2-hour plasma glucose from baseline to 24-months in DPP compared with non-DPP patients
Primary 2-hour plasma glucose Lab values extracted from electronic health record Change in 2-hour plasma glucose from baseline to 30-months in DPP compared with non-DPP patients
Primary 2-hour plasma glucose Lab values extracted from electronic health record Change in 2-hour plasma glucose from baseline to 36-months in DPP compared with non-DPP patients
Primary Medical encounters Extracted from electronic health record Number of medical encounters between baseline and 6-months in DPP compared with non-DPP patients
Primary Medical encounters Extracted from electronic health record Number of medical encounters between baseline and 12-months in DPP compared with non-DPP patients
Primary Medical encounters Extracted from electronic health record Number of medical encounters between baseline and 18-months in DPP compared with non-DPP patients
Primary Medical encounters Extracted from electronic health record Number of medical encounters between baseline and 24-months in DPP compared with non-DPP patients
Primary Medical encounters Extracted from electronic health record Number of medical encounters between baseline and 30-months in DPP compared with non-DPP patients
Primary Medical encounters Extracted from electronic health record Number of medical encounters between baseline and 36-months in DPP compared with non-DPP patients
Primary Medical expenditures Total dollar amount billed per encounter extracted from electronic health record Medical expenditures from baseline to 6-months in DPP compared with non-DPP patients
Primary Medical expenditures Total dollar amount billed per encounter extracted from electronic health record Medical expenditures from baseline to 12-months in DPP compared with non-DPP patients
Primary Medical expenditures Total dollar amount billed per encounter extracted from electronic health record Medical expenditures from baseline to 18-months in DPP compared with non-DPP patients
Primary Medical expenditures Total dollar amount billed per encounter extracted from electronic health record Medical expenditures from baseline to 24-months in DPP compared with non-DPP patients
Primary Medical expenditures Total dollar amount billed per encounter extracted from electronic health record Medical expenditures from baseline to 30-months in DPP compared with non-DPP patients
Primary Medical expenditures Total dollar amount billed per encounter extracted from electronic health record Medical expenditures from baseline to 36-months in DPP compared with non-DPP patients
Secondary Body weight Total body weight measured using Seca mBCA 554 Change in body weight from baseline to 6-months
Secondary Body weight Total body weight measured using Seca mBCA 554 Change in body weight from baseline to 12-months
Secondary Body weight Total body weight measured using Seca mBCA 554 Change in body weight from baseline to 24-months
Secondary Body weight Total body weight measured using Seca mBCA 554 Change in body weight from baseline to 36-months
Secondary Fat mass Total body fat mass measured using Seca mBCA 554; bioimpedance analysis Change in fat mass from baseline to 6-months
Secondary Fat mass Total body fat mass measured using Seca mBCA 554; bioimpedance analysis Change in fat mass from baseline to 12-months
Secondary Fat mass Total body fat mass measured using Seca mBCA 554; bioimpedance analysis Change in fat mass from baseline to 24-months
Secondary Fat mass Total body fat mass measured using Seca mBCA 554; bioimpedance analysis Change in fat mass from baseline to 36-months
Secondary Visceral fat Visceral fat measured using Seca mBCA 554; bioimpedance analysis Change in visceral fat from baseline to 6-months
Secondary Visceral fat Visceral fat measured using Seca mBCA 554; bioimpedance analysis Change in visceral fat from baseline to 12-months
Secondary Visceral fat Visceral fat measured using Seca mBCA 554; bioimpedance analysis Change in visceral fat from baseline to 24-months
Secondary Visceral fat Visceral fat measured using Seca mBCA 554; bioimpedance analysis Change in visceral fat from baseline to 36-months
Secondary Skeletal muscle mass Total body skeletal muscle mass measured using Seca mBCA 554; bioimpedance analysis Change in skeletal muscle mass from baseline to 6-months
Secondary Skeletal muscle mass Total body skeletal muscle mass measured using Seca mBCA 554; bioimpedance analysis Change in skeletal muscle mass from baseline to 12-months
Secondary Skeletal muscle mass Total body skeletal muscle mass measured using Seca mBCA 554; bioimpedance analysis Change in skeletal muscle mass from baseline to 24-months
Secondary Skeletal muscle mass Total body skeletal muscle mass measured using Seca mBCA 554; bioimpedance analysis Change in skeletal muscle mass from baseline to 36-months
Secondary Waist circumference Measures using Seca 203 circumference measuring tape Change in waist circumference from baseline to 6-months
Secondary Waist circumference Measures using Seca 203 circumference measuring tape Change in waist circumference from baseline to 12-months
Secondary Waist circumference Measures using Seca 203 circumference measuring tape Change in waist circumference from baseline to 24-months
Secondary Waist circumference Measures using Seca 203 circumference measuring tape Change in waist circumference from baseline to 36-months
Secondary Systolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in systolic blood pressure from baseline to 6-months
Secondary Systolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in systolic blood pressure from baseline to 12-months
Secondary Systolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in systolic blood pressure from baseline to 24-months
Secondary Systolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in systolic blood pressure from baseline to 36-months
Secondary Diastolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in diastolic blood pressure from baseline to 6-months
Secondary Diastolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in diastolic blood pressure from baseline to 12-months
Secondary Diastolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in diastolic blood pressure from baseline to 24-months
Secondary Diastolic blood pressure Welch Allyn blood pressure unit following the American Heart Association guidelines for adults. Change in diastolic blood pressure from baseline to 36-months
Secondary Resting heart rate Welch Allyn blood pressure unit. Change in resting heart rate from baseline to 6-months
Secondary Resting heart rate Welch Allyn blood pressure unit. Change in resting heart rate from baseline to 12-months
Secondary Resting heart rate Welch Allyn blood pressure unit. Change in resting heart rate from baseline to 24-months
Secondary Resting heart rate Welch Allyn blood pressure unit. Change in resting heart rate from baseline to 36-months
Secondary Total cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in total cholesterol from baseline to 6-months
Secondary Total cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in total cholesterol from baseline to 12-months
Secondary Total cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in total cholesterol from baseline to 24-months
Secondary Total cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in total cholesterol from baseline to 36-months
Secondary HDL cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in HDL cholesterol from baseline to 6-months
Secondary HDL cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in HDL cholesterol from baseline to 12-months
Secondary HDL cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in HDL cholesterol from baseline to 24-months
Secondary HDL cholesterol PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in HDL cholesterol from baseline to 36-months
Secondary Triglycerides PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in triglycerides from baseline to 6-months
Secondary Triglycerides PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in triglycerides from baseline to 12-months
Secondary Triglycerides PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in triglycerides from baseline to 24-months
Secondary Triglycerides PTS Diagnostics CardioChek Plus analyzer; point of care finger stick to obtain 40 µL blood Change in triglycerides from baseline to 36-months
Secondary Hemoglobin A1c (point of care) A1CNOW+ System for reliable point-of-care HbA1c measurement; non-fasting 5 µL blood Change in HbA1c from baseline to 6-months
Secondary Hemoglobin A1c (point of care) A1CNOW+ System for reliable point-of-care HbA1c measurement; non-fasting 5 µL blood Change in HbA1c from baseline to 12-months
Secondary Hemoglobin A1c (point of care) A1CNOW+ System for reliable point-of-care HbA1c measurement; non-fasting 5 µL blood Change in HbA1c from baseline to 24-months
Secondary Hemoglobin A1c (point of care) A1CNOW+ System for reliable point-of-care HbA1c measurement; non-fasting 5 µL blood Change in HbA1c from baseline to 36-months
Secondary Self-efficacy for weight loss and maintenance Weight self-efficacy lifestyle questionnaire; 20 items using a 10-point Likert scale; higher mean score indicates higher self-efficacy; Clark et al., 1991 Change in self-efficacy from baseline to 6-months
Secondary Self-efficacy for weight loss and maintenance Weight self-efficacy lifestyle questionnaire; 20 items using a 10-point Likert scale; higher mean score indicates higher self-efficacy; Clark et al., 1991 Change in self-efficacy from baseline to 12-months
Secondary Self-efficacy for weight loss and maintenance Weight self-efficacy lifestyle questionnaire; 20 items using a 10-point Likert scale; higher mean score indicates higher self-efficacy; Clark et al., 1991 Change in self-efficacy from baseline to 24-months
Secondary Self-efficacy for weight loss and maintenance Weight self-efficacy lifestyle questionnaire; 20 items using a 10-point Likert scale; higher mean score indicates higher self-efficacy; Clark et al., 1991 Change in self-efficacy from baseline to 36-months
Secondary Readiness to change, stage of change Stages of Change in Overweight and Obese People questionnaire (S-weight); 1-item with 5 distinct and mutually exclusive responses to measure stage of change; Andres et al., 2009 Change in stage of change from baseline to 6-months
Secondary Readiness to change, stage of change Stages of Change in Overweight and Obese People questionnaire (S-weight); 1-item with 5 distinct and mutually exclusive responses to measure stage of change; Andres et al., 2009 Change in stage of change from baseline to 12-months
Secondary Readiness to change, stage of change Stages of Change in Overweight and Obese People questionnaire (S-weight); 1-item with 5 distinct and mutually exclusive responses to measure stage of change; Andres et al., 2009 Change in stage of change from baseline to 24-months
Secondary Readiness to change, stage of change Stages of Change in Overweight and Obese People questionnaire (S-weight); 1-item with 5 distinct and mutually exclusive responses to measure stage of change; Andres et al., 2009 Change in stage of change from baseline to 36-months
Secondary Readiness to change, processes of change Processes of Change in Overweight and Obese People questionnaire (P-weight); 34 items; 5-point Likert scale from Strongly Disagree to Strongly Agree where higher mean score indicates higher use of respective process; four processes include emotional re-evaluation, weight consequences evaluation, supporting relationships, and weight management actions across 4 processes of change; Andres et al., 2011 Change in processes of change from baseline to 6-months
Secondary Readiness to change, processes of change Processes of Change in Overweight and Obese People questionnaire (P-weight); 34 items; 5-point Likert scale from Strongly Disagree to Strongly Agree where higher mean score indicates higher use of respective process; four processes include emotional re-evaluation, weight consequences evaluation, supporting relationships, and weight management actions across 4 processes of change; Andres et al., 2011 Change in processes of change from baseline to 12-months
Secondary Readiness to change, processes of change Processes of Change in Overweight and Obese People questionnaire (P-weight); 34 items; 5-point Likert scale from Strongly Disagree to Strongly Agree where higher mean score indicates higher use of respective process; four processes include emotional re-evaluation, weight consequences evaluation, supporting relationships, and weight management actions across 4 processes of change; Andres et al., 2011 Change in processes of change from baseline to 24-months
Secondary Readiness to change, processes of change Processes of Change in Overweight and Obese People questionnaire (P-weight); 34 items; 5-point Likert scale from Strongly Disagree to Strongly Agree where higher mean score indicates higher use of respective process; four processes include emotional re-evaluation, weight consequences evaluation, supporting relationships, and weight management actions across 4 processes of change; Andres et al., 2011 Change in processes of change from baseline to 36-months
Secondary Decisional balance Decisional balance inventory; 20 items using 5-point Likert scale to identify cognitive and emotional pros and cons to making intentional changes for weight loss and maintenance (Not Important At All to Extremely Important); higher mean scores for subscales (Pros; Pro-Con) would indicate higher intention; O'Connell and Velicer, 1988 Change in decisional balance from baseline to 6-months
Secondary Decisional balance Decisional balance inventory; 20 items using 5-point Likert scale to identify cognitive and emotional pros and cons to making intentional changes for weight loss and maintenance (Not Important At All to Extremely Important); higher mean scores for subscales (Pros; Pro-Con) would indicate higher intention; O'Connell and Velicer, 1988 Change in decisional balance from baseline to 12-months
Secondary Decisional balance Decisional balance inventory; 20 items using 5-point Likert scale to identify cognitive and emotional pros and cons to making intentional changes for weight loss and maintenance (Not Important At All to Extremely Important); higher mean scores for subscales (Pros; Pro-Con) would indicate higher intention; O'Connell and Velicer, 1988 Change in decisional balance from baseline to 24-months
Secondary Decisional balance Decisional balance inventory; 20 items using 5-point Likert scale to identify cognitive and emotional pros and cons to making intentional changes for weight loss and maintenance (Not Important At All to Extremely Important); higher mean scores for subscales (Pros; Pro-Con) would indicate higher intention; O'Connell and Velicer, 1988 Change in decisional balance from baseline to 36-months
Secondary Self-efficacy for overcoming barriers to physical activity and healthy eating Self-efficacy for overcoming barriers to physical activity and diet; 10 items using a 4-point Likert scale from Very Uncertain to Very Certain or Not True At All to Exactly True; higher mean score (20 to 80) indicated greater self-efficacy; Huttunen-Lenz et al., 2018 Change in barrier self-efficacy from baseline to 6-months
Secondary Self-efficacy for overcoming barriers to physical activity and healthy eating Self-efficacy for overcoming barriers to physical activity and diet; 10 items using a 4-point Likert scale from Very Uncertain to Very Certain or Not True At All to Exactly True; higher mean score (20 to 80) indicated greater self-efficacy; Huttunen-Lenz et al., 2018 Change in barrier self-efficacy from baseline to 12-months
Secondary Self-efficacy for overcoming barriers to physical activity and healthy eating Self-efficacy for overcoming barriers to physical activity and diet; 10 items using a 4-point Likert scale from Very Uncertain to Very Certain or Not True At All to Exactly True; higher mean score (20 to 80) indicated greater self-efficacy; Huttunen-Lenz et al., 2018 Change in barrier self-efficacy from baseline to 24-months
Secondary Self-efficacy for overcoming barriers to physical activity and healthy eating Self-efficacy for overcoming barriers to physical activity and diet; 10 items using a 4-point Likert scale from Very Uncertain to Very Certain or Not True At All to Exactly True; higher mean score (20 to 80) indicated greater self-efficacy; Huttunen-Lenz et al., 2018 Change in barrier self-efficacy from baseline to 36-months
Secondary Self-regulation of eating behaviors Self-regulation of Eating Behavior Questionnaire; 5 items using a 5-point Likert scale; mean score <2.8, 2.8 - 3.6, >3.6 correspond to low, medium and high self-regulation, respectively; Kliemann et al., 2016 Change in self-regulation of eating behaviors from baseline to 6-months
Secondary Self-regulation of eating behaviors Self-regulation of Eating Behavior Questionnaire; 5 items using a 5-point Likert scale; mean score <2.8, 2.8 - 3.6, >3.6 correspond to low, medium and high self-regulation, respectively; Kliemann et al., 2016 Change in self-regulation of eating behaviors from baseline to 12-months
Secondary Self-regulation of eating behaviors Self-regulation of Eating Behavior Questionnaire; 5 items using a 5-point Likert scale; mean score <2.8, 2.8 - 3.6, >3.6 correspond to low, medium and high self-regulation, respectively; Kliemann et al., 2016 Change in self-regulation of eating behaviors from baseline to 24-months
Secondary Self-regulation of eating behaviors Self-regulation of Eating Behavior Questionnaire; 5 items using a 5-point Likert scale; mean score <2.8, 2.8 - 3.6, >3.6 correspond to low, medium and high self-regulation, respectively; Kliemann et al., 2016 Change in self-regulation of eating behaviors from baseline to 36-months
Secondary Self-regulation of physical activity - goals Exercise goal-setting scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity goals from baseline to 6-months
Secondary Self-regulation of physical activity - goals Exercise goal-setting scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity goals from baseline to 12-months
Secondary Self-regulation of physical activity - goals Exercise goal-setting scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity goals from baseline to 24-months
Secondary Self-regulation of physical activity - goals Exercise goal-setting scale; 10 items using 5-point Likert scale from Does Not Exercise goal-setting scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity goals from baseline to 36-months
Secondary Self-regulation of physical activity - planning Exercise planning and scheduling scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity planning from baseline to 6-months
Secondary Self-regulation of physical activity - planning Exercise planning and scheduling scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity planning from baseline to 12-months
Secondary Self-regulation of physical activity - planning Exercise planning and scheduling scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity planning from baseline to 24-months
Secondary Self-regulation of physical activity - planning Exercise planning and scheduling scale; 10 items using 5-point Likert scale from Does Not Describe Me (0) to Describes Me Completely (4); higher mean score reflects greater self-regulation Rovniak et al., 2002 Change in self-regulation of physical activity planning from baseline to 36-months
Secondary Social support from friends - eating Friend social support for healthy eating scale; 10 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 6-months
Secondary Social support from friends - eating Friend social support for healthy eating scale; 10 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 12-months
Secondary Social support from friends - eating Friend social support for healthy eating scale; 10 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 24-months
Secondary Social support from friends - eating Friend social support for healthy eating scale; 10 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 36-months
Secondary Social support from family - eating Family social support for healthy eating scale; 13 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 6-months
Secondary Social support from family - eating Family social support for healthy eating scale; 13 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 12-months
Secondary Social support from family - eating Family social support for healthy eating scale; 13 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 24-months
Secondary Social support from family - eating Family social support for healthy eating scale; 13 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 36-months
Secondary Social support from friend - physical activity Friend social support for physical activity scale; 9-items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 6-months
Secondary Social support from friend - physical activity Friend social support for physical activity scale; 9-items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 12-months
Secondary Social support from friend - physical activity Friend social support for physical activity scale; 9-items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 24-months
Secondary Social support from friend - physical activity Friend social support for physical activity scale; 9-items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 36-months
Secondary Social support from family - physical activity Family social support for physical activity scale; 15 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 6-months
Secondary Social support from family - physical activity Family social support for physical activity scale; 15 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 12-months
Secondary Social support from family - physical activity Family social support for physical activity scale; 15 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 24-months
Secondary Social support from family - physical activity Family social support for physical activity scale; 15 items using a 5-point Likert scale from None of the Time (1) to All of the Time (5) where a higher mean score indicated greater social support; Sallis et al., 1987 Change in social support from baseline to 36-months
Secondary Outcome expectancies Outcome expectancies of behavior change; 25 items using 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicating greater outcome expectancy; Huttunen-Lenz et al., 2018 Change in outcome expectancies from baseline to 6-months
Secondary Outcome expectancies Outcome expectancies of behavior change; 25 items using 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicating greater outcome expectancy; Huttunen-Lenz et al., 2018 Change in outcome expectancies from baseline to 12-months
Secondary Outcome expectancies Outcome expectancies of behavior change; 25 items using 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicating greater outcome expectancy; Huttunen-Lenz et al., 2018 Change in outcome expectancies from baseline to 24-months
Secondary Outcome expectancies Outcome expectancies of behavior change; 25 items using 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicating greater outcome expectancy; Huttunen-Lenz et al., 2018 Change in outcome expectancies from baseline to 36-months
Secondary Coping self-efficacy Coping self-efficacy scale; 14 items using a 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicates greater self-efficacy for coping; Huttunen-Lenz et al., 2018 Change in coping self-efficacy from baseline to 6-months
Secondary Coping self-efficacy Coping self-efficacy scale; 14 items using a 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicates greater self-efficacy for coping; Huttunen-Lenz et al., 2018 Change in coping self-efficacy from baseline to 12-months
Secondary Coping self-efficacy Coping self-efficacy scale; 14 items using a 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicates greater self-efficacy for coping; Huttunen-Lenz et al., 2018 Change in coping self-efficacy from baseline to 24-months
Secondary Coping self-efficacy Coping self-efficacy scale; 14 items using a 4-point Likert scale from Not True At All (1) to Exactly True (4); higher mean score indicates greater self-efficacy for coping; Huttunen-Lenz et al., 2018 Change in coping self-efficacy from baseline to 36-months
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