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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02266576
Other study ID # SU-30015
Secondary ID PCORI-PCORIAD-13
Status Completed
Phase N/A
First received
Last updated
Start date June 2015
Est. completion date August 30, 2017

Study information

Verified date December 2019
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of the proposed research is to identify effective patient-centered strategies to prevent diabetes in high-risk populations in real world settings. The investigators will accomplish this by conducting a randomized controlled trial comparing an enhanced Diabetes Prevention Program addressing psychosocial stressors to a standard version in a high-risk population of urban American Indian and Alaska Native people within a primary care setting.


Description:

The goal of the proposed research is to identify effective patient-centered strategies to prevent diabetes in high-risk populations in real world settings. The investigators will accomplish this by conducting a randomized controlled trial comparing an enhanced Diabetes Prevention Program addressing psychosocial stressors to a standard version in a high-risk population of urban American Indian and Alaska Native peoples within a primary care setting. Diabetes is disproportionately prevalent among low-socioeconomic status and racial/ethnic minority populations in the US. The high prevalence of psychosocial stressors such as depression, discrimination, and exposure to trauma among these populations contributes to the high prevalence of diabetes and interferes with successful completion of lifestyle interventions. The investigators hypothesize that a DPP that directly addresses these psychosocial stressors will be superior to the standard DPP in addressing this disparity in diabetes.


Recruitment information / eligibility

Status Completed
Enrollment 207
Est. completion date August 30, 2017
Est. primary completion date August 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Urban of Indigenous Ancestry from the Americas (North, Central and South America)

- Men and women

- BMI Between 30-55

- Not diagnosed with Type II Diabetes

- At least one of the following criterion

1. Triglycerides: 150mg/dL or higher

2. Reduced HDL: <40mg/dL (men); <50mg/dL (women)

3. Blood pressure: >130/80 or current treatment with antihypertensives

4. Fasting glucose: >100mg/dL

Exclusion Criteria:

- Significant medical comorbidities, including uncontrolled metabolic disorders (e.g., thyroid, diabetes, renal, liver), unstable heart disease, heart failure, and ongoing substance abuse;

- On greater than 10 prescription medications.

- Psychiatric disorders requiring atypical antipsychotics or multiple medications;

- Inappropriate for moderate exercise according to the Revised Physical Activity Readiness Questionnaire;

- Pregnant, planning to become pregnant, or lactating;

- Family household member already enrolled in the study;

- Already enrolled or planning to enroll in a clinical trial that would limit full participation in the study;

- Resident of a long term care facility;

- Lack of spoken English by patient or a household member > 18 y who can serve as interpreter;

- Plans to move during the study period (9 months post-randomization);

- Investigator discretion for clinical safety or adherence reasons (e.g., unstable housing, chronic pain).

Study Design


Intervention

Behavioral:
Standard DPP
The Standard Diabetes Prevention Program (DPP) delivered by the San Jose State Timpany Center is the Group Lifestyle Balanceā„¢ DPP, which has previously been tailored for urban American Indians and Alaska Natives by the Indian Health Service. Standard DPP components consist of 16 group classes, 4 visits with a lifestyle coach and access to a therapeutic swimming pool and gym.
Enhanced DPP
Enhanced DPP components consist of access to a mental health counselor, active referrals to mental health services, and traditional healing workshops such as the use of talking circles, a modified photo voice and digital storytelling to address specific psychosocial issues that are a result of historical trauma, stress, and grief.

Locations

Country Name City State
United States Timpany Center of San Jose State University San Jose California
United States Stanford University School of Medicine Stanford California

Sponsors (3)

Lead Sponsor Collaborator
Stanford University Patient-Centered Outcomes Research Institute, San Jose State University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Rosas LG, Vasquez JJ, Naderi R, Jeffery N, Hedlin H, Qin F, LaFromboise T, Megginson N, Pasqua C, Flores O, McClinton-Brown R, Evans J, Stafford RS. Development and evaluation of an enhanced diabetes prevention program with psychosocial support for urban American Indians and Alaska natives: A randomized controlled trial. Contemp Clin Trials. 2016 Sep;50:28-36. doi: 10.1016/j.cct.2016.06.015. Epub 2016 Jul 2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Systolic Blood Pressure Blood pressure readings are expressed in millimeters of mercury. This unit is abbreviated as mm Hg. A normal reading would be any blood pressure below 120/80 mm Hg and above 90/60 mm Hg in an adult. Baseline, 6 months and 12 months
Other Diastolic Blood Pressure Blood pressure readings are expressed in millimeters of mercury (mmHg). A normal reading would be any blood pressure below 120/80 mm Hg and above 90/60 mm Hg in an adult. Baseline, 6 months and 12 months
Other Fasting Blood Glucose Performed via fasting participant finger stick with Alere Cholestech LDX POS device. Baseline, 6 months and 12 months
Other Symptoms of Historical Trauma By patient report using a modified version of the Indigenous People's Survey Baseline, 6 months and 12 months
Other Waist Circumference In centimeters, measured by trained assessor using standard protocol Baseline, 6 months and 12 months
Other Lipid Bioassays LDL-cholesterol, HDL-cholesterol, and Triglycerides; performed via fasting participant finger stick with Alere Cholestech LDX POS device Baseline, 6 months and 12 months
Primary Change From Baseline in Body Mass Index (BMI) Through Month 12 BMI is measured as weight in kg divided by the square of height in meters. Change through month 12, with assessments at baseline, 6 months, and 12 months
Primary Change From Baseline in the Quality of Life Short Form Survey (SF-12) SF-12 scale is a generic, multipurpose short-form survey with 12 questions selected from the SF-36 Health Survey to evaluate overall health-related quality of life. Answers are combined, scored and weighted into mental and physical functioning component scales. The scores for each scale range from 0 to 100. A higher value indicates a better quality of life of the patient. Change through month 12, with assessments at baseline, 6 months, and 12 months
Secondary Change From Baseline in Food Frequency Questionnaire (FFQ) Score as a Measure of Healthy and Unhealthy Diet Choices The FFQ modified to incorporate culturally-relevant food choices (e.g. corn tortillas and frybread) was used. Food items were scored on a scale of 1 to 6 (6 corresponding to the greatest frequency of consumption), and categorized as "healthy," "unhealthy," and "undetermined" based on classifications previously determined by Teuful-Shone et al. "Healthy" foods were those recommended for increased intake (e.g. green leafy salad). "Unhealthy" foods were recommended for decreased intake (e.g. soft drinks), and all remaining foods were "undetermined." Healthy and unhealthy food scores (but not undetermined) were collected for this outcome measure. Scores were summed for a total score. Healthy food choices (6 questions) score range 3-36 (higher scores mean healthier diet). Unhealthy food choices (13 questions) score range: 13-78 (lower scores mean healthier diet). Change through month 12, with assessments at baseline, 6 months, and 12 months
Secondary Change From Baseline in Physical Activity Measured in Metabolic Equivalents (MET) Per Week MET is a term used to represent the intensity of exercise. A MET is the ratio of the rate of energy expended during an activity to the rate of energy expended at rest. At least 1000 MET minutes per week are needed to lower the risk of disease.
1 minute of light-intensity activities = 1.1 MET to 2.9 METs
1 minute of moderate-intensity activities = 3.0 to 5.9 METs
1 minute of vigorous-intensity activities = 6.0 METs or more
Change through month 12, with assessments at baseline, 6 months, and 12 months
Secondary Change From Baseline in the Center for Epidemiologic Studies - Depression Scale (CES-D) as a Measure of Mental Health Symptoms The CES-D (Radloff, 1977) is a 20-item, self-report scale designed to assess the presence and severity of depressive symptoms over the past week. The total range is 0-80, with higher scores reflecting more severe depression symptoms. Change through month 12, with assessments at baseline, 6 months, and 12 months
Secondary Change in From Baseline in Empowerment The Growth and Empowerment Measure (GEM) was developed to measure change in dimensions of empowerment as defined and described by Aboriginal Australians who participated in the Family Well Being programme. The GEM has two components. The 14-item Emotional Empowerment Scale has a range of 12-60, with higher scores corresponding to more ability to feel and show the signs of empowerment . The 12-item Scenarios scale has a range of 12-84, with higher scores corresponding to better emotional empowerment in different scenarios. Change through month 12, with assessments at baseline, 6 months, and 12 months
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