Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06440551
Other study ID # 0048231
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 15, 2024
Est. completion date May 31, 2026

Study information

Verified date May 2024
Source Medical College of Wisconsin
Contact Lisa Sanchez-Johnsen, PhD
Phone 414-955-8057
Email LSanchezJohnsen@mcw.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to address the high rates of overweight/obesity in Puerto Rican (PR) men. The main question it aims to answer is whether virtual culturally relevant classes supporting physical activity and healthy eating for Puerto Rican men at different levels of acculturation to the US culture, will help these men achieve clinically meaningful weight loss. The purpose of this project is to assess whether a virtual intervention tailored for Puerto Rican men that includes information about healthy eating, physical activity, sedentary behavior is feasible and acceptable compared to a general health (GH) intervention. It is also to determine whether this intervention leads to healthier eating, increased physical activity, less sedentary behavior (low activity), and clinically meaningful weight loss. Hypothesis 1: Test the feasibility (recruitment, retention, adherence, fidelity) and acceptability (treatment components, intervention leaders, telehealth modality, technology and equipment, intervention satisfaction, satisfaction with randomized study, and measures) of a randomized 4-month synchronous telehealth lifestyle intervention led by a community health promoter and behavioral health specialist, who will receive either: TeleSalud HE-PA/SB" or TeleSalud GH in 48 PR men. Hypothesis 2: Demonstrate proof -of-concept by achieving a clinically significant weight reduction of ≥ 5% of baseline weight in the TeleSalud HE-PA/SB intervention after 4 months and at the end of the 4-month maintenance compared to the TeleSalud General Health intervention. Researchers will compare this to a group that will receive information about general health topics - not healthy eating or physical activity. - Participants in both groups will meet via virtually for 4 months (twice per week for 3 months and once per week for 1 month). - Participants will then meet one per month for a maintenance session for the next 4 months.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 48
Est. completion date May 31, 2026
Est. primary completion date May 15, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 35 Years and older
Eligibility Inclusion Criteria: - Male of Puerto Rican descent over 35 years. - BMI =25 by anthropometrically measured weight and height. - Physically able to exercise (via the EASY tool or, if needed, able to receive medical clearance to participate in the study). - Has access to secure computer or tablet in a private location with reliable internet connection to support video streaming - Ability to understand and speak English and Spanish. Exclusion Criteria: - Does not understand/speak English or Spanish. - Plans to move from the Illinois area during the study. - Currently in a formal weight management program. - Current or planned use of weight control or loss medication prescribed by a doctor. - Currently exercising >1 time/week. - Unable to attend study times. - Serious medical problems or medications that would make protocol compliance difficult or dangerous, e.g., unable to engage in moderate & eventually vigorous exercise, uncontrolled diabetes (A1C > 9) or hypertension (systolic >160 or diastolic >100), hypoglycemia, heart attack in the past six months, unstable angina, life-threatening arrhythmias, cancer that required treatment in the last 5 years (except non-melanoma skin cancers that have been cured). - Current alcohol abuse (>35 alcoholic drinks/week); score of yes to > 2 questions on the CAGE alcohol scale. - Current recreational or illegal drug use.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
TeleSalud Healthy Eating- Physical Activity/Sedentary Behavior (HE-PA/SB)
Participants will meet via telehealth for 4 months (twice a week for 3 months and then once per week for 1 month) for a TeleSalud HE-PA/SB Class, after which they will attend one maintenance meeting per month for 4 months. Weekly, Day 1 (Healthy Eating & PA-SB Class): Participants will receive a 50-min. healthy eating class. Physical Activity- Sedentary Behavior (PA-SB) Class: By discussing barriers and strategies to overcome barriers, this will help to increase self-efficacy. We will engage in Latino-centered moderate impact (increasing to vigorous) aerobics with Latino or salsa movements and music for 45-50 minutes. Aspects of kickboxing aerobics will be integrated. Goal: Exercise a minimum of 150-250 min./ week of moderate intensity. Weekly, Day 2: PA-SB identical PA-SB to Day 1. Maintenance (Months 5-8): Meetings once/ month for 70 min. for HE/PA-SB class, including 25 min. to discuss diet and PA-SB barriers. Goal: Exercise a minimum of 150-250 min./week.
TeleSalud General Health Intervention
Weekly: Participants will meet via telehealth for 4 months (twice a week for 3 months and then once per week for 1 month) for a TeleSalud General Heath Class, after which they will attend one maintenance meeting per month for 4 months. Participants will meet and discuss general health topics (not diet or PA). Examples of the general health topics are: Back Pain, Muscle Strains, Alcohol Use, Stress & Coping, Oral and Dental Health, Safety Tips, Emergency Preparedness. The content is relevant to Latinos, and information is focused on Latino men. Maintenance (Months 5-8): Participants will meet via telehealth once/ month for 70 min. to discuss general health topics. To enhance motivation to complete the study and assessments, this group will receive a copy of the TeleSalud HE-PA/SB intervention manual and related materials after the maintenance period ends.

Locations

Country Name City State
United States Medical College of Wisconsin Milwaukee Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
Medical College of Wisconsin

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability- Fidelity: Delivery Delivery will be measured by an adherence checklist. It will monitor consistency and accuracy in the delivery of the intervention. 4 months, 8 months
Primary Acceptability- Fidelity: Receipt Receipt will be measured by participants' self-reports of understanding and knowledge acquisition of content for both groups. 4 months, 8 months
Primary Acceptability- Fidelity: Enactment Enactment will be measured by participants' self-report of changes in behavior based on targets of treatment (e.g., Healthy Eating, Physical Activity, and Sedentary Behavior, General Health.) 4 months, 8 months
Primary Acceptability- Helpfulness of Treatment Components Perceived helpfulness/ effectiveness of various treatment components (12 questions, on a 5- point Likert scale: not at all to extremely effective) will be assessed. The average of the treatment component questions will be used as the overall dependent measure of the acceptability of the treatment components. 4 months, 8 months
Primary Acceptability- Helpfulness/ Effectiveness of the Intervention Leaders Perceived helpfulness/ effectiveness of the intervention leaders (6 questions, on a 5-point Likert scale: not at alll to extremely helpful) will be assessed. The average of the questions will be used as the overall dependent measures of the acceptability of the intervention leaders. 4 months, 8 months
Primary Acceptability- Intervention Satisfaction Acceptability- Assessed by an intervention satisfaction questionnaire (14 questions, on a 5- point Likert scale: not at all satisfied to extremely satisfied). 4 months, 8 months
Primary Acceptability- Perceived Helpfulness/ Effectiveness of the Telehealth Modality, Technology, and Equipment Perceived helpfulness/ effectiveness of the telehealth modality, technology and equipment (3 questions, on 5-point Likert scale: not at all to extremely effective) will be assessed. The average of the telehealth components questions will be used as the overall dependent measure of the acceptability of the telehealth components. Baseline, 4 months, 8 months
Primary Acceptability- Satisfaction with Random Assignment to Groups Acceptability- Assessed by a questionnaire assessing satisfaction with being in a study with random assignment to groups (14 questions, on a 5-point Likert scale: not at all satisfied to extremely satisfied). Baseline, 4 months, 8 months
Primary Dietary Intake: Number of Servings of Fruits Changes in number of servings of fruits will be measured by the Automated Self-Administered 24- Hour (ASA24) Dietary Assessment Tool. Baseline, 4 months, 8 months
Primary Dietary Intake: Number of Servings of Vegetables Change in number of servings of vegetables will be measured by the Automated Self-Administered 24- Hour (ASA24) Dietary Assessment Tool. Baseline, 4 months, 8 months
Primary Dietary Intake: Percent of Calories from Saturated Fat Changes in percent of calories from saturated fat will be measured by the Automated Self-Administered 24-Hour (ASA24) Dietary Assessment Tool. Baseline, 4 months, 8 months
Primary Dietary Intake: Total Energy Intake Changes in total energy intake will be measured by the Automated Self-Administered 24-Hour (ASA24) Dietary Assessment Tool. Baseline, 4 months, 8 months
Primary Feasibility- Adherence- Monthly Attendance Feasibility- Adherence- Monthly: Will be measured by the frequency of attendance at each session on a monthly basis. 4 months, 8 months
Primary Feasibility- Adherence- Number of Make-Up Sessions Feasibility- Adherence- Number of Make-Up Sessions: Will be assessed by frequency/counts of number of make-up sessions. 4 months, 8 months
Primary Feasibility- Adherence- Number of Missed Sessions Overall Feasibility- Adherence- Number of Missed Sessions Overall: Will be assessed by frequency/ counts of the number of missed sessions overall (no make-up sessions). 4 months, 8 months
Primary Feasibility- Adherence- Weekly Attendance Feasibility- Adherence- Weekly Attendance: Will be measured by the frequency of attendance at each session on a weekly basis. 4 months, 8 months
Primary Feasibility- Recruitment- Number Enrolled Recruitment feasibility assessed by the number of participants enrolled. Pre-Intervention
Primary Feasibility- Recruitment- Number of Contacts Recruitment feasibility assessed by counts of the number of contacts. Pre-Intervention
Primary Feasibility- Recruitment- Rate of Consenting Recruitment feasibility assessed by the rate of consenting. Pre-Intervention
Primary Feasibility- Recruitment- Rate of Enrollment Recruitment feasibility assessed by the rate of enrollment. Pre-Intervention
Primary Feasibility- Recruitment- Rate of Screening Recruitment feasibility assessed by the rate of screening. Pre-Intervention
Primary Feasibility- Recruitment- Recruitment Method Feasibility assessed by tracking the method of recruitment. Pre-Intervention
Primary Feasibility- Recruitment- Response Rate Recruitment feasibility assessed by rate of response. Pre-Intervention
Primary Feasibility- Recruitment- Type of Contact Recruitment feasibility assessed by tracking the type of contact. Pre-Intervention
Primary Feasibility- Retention- Number Completed the intervention Retention assessed by counts and frequency of the number who completed the interventions. 4 months, 8 months
Primary Feasibility- Recruitment- Number Screened Recruitment feasibility assessed by the count of number of individuals screened. Pre-Intervention
Primary Feasibility- Retention- Number of Classes Attended Retention- assessed by counts of the number of classes attended. 4 months, 8 months
Primary Feasibility- Retention- Percent Completed the Interventions Retention assessed by the percent of participants who completed the interventions. 4 months, 8 months
Primary Feasibility- Retention- Percent of Classes Attended Retention assessed by percent of classes attended. 4 months, 8 months
Primary Feasibility- Recruitment- Number Consented Recruitment feasibility assessed by the number of participants who consented. Pre-Intervention
Primary Objective Physical Activity (Accelerometer) A triaxial wrist accelerometer (ActiGraph wGT3XBT) will measure objective physical activity. They will used the accelerometer during waking hours for 7 days on their non-dominant wrist. Baseline, 4 months, 8 months
Primary Subjective Physical Activity (International Physical Activity Questionnaire) The International Physical Activity Questionnaire long form- will measure sedentary and leisure and non-leisure time physical activity. Baseline, 4 months, 8 months
Primary Subjective Sedentary Behavior (International Physical Activity Questionnaire) The International Physical Activity Questionnaire long form- will measure sedentary and leisure and non-leisure time physical activity. Baseline, 4 months, 8 months
Secondary Body Mass Index Body Mass Index (BMI) will be assessed by objectively measured height and weight. Baseline, 4 months, 8 months
Secondary Outcome Expectations for Diet Questionnaire Outcome expectations will be assessed by the Outcome Expectations for Diet Questionnaire. This measure will be used to assess the various components of Social Cognitive Theory which are guiding the TeleSalud HE-PA/SB intervention. Baseline, 4 months, 8 months
Secondary Exercise Outcomes on the Outcomes Expectations Questionnaire Outcome expectations for Exercise will be assessed by the Exercise Outcomes on the Outcomes Expectations Questionnaire. This measure will be used to assess the various components of Social Cognitive Theory which are guiding the TeleSalud HE-PA/SB intervention. Baseline, 4 months, 8 months
Secondary Self-Efficacy for Dietary Behaviors Self-efficacy will be assessed by the Self-Efficacy for Dietary Behaviors. This measure will be used to assess the various components of Social Cognitive Theory which are guiding the TeleSalud HE-PA/SB intervention. Baseline, 4 months, 8 months
Secondary Exercise Confidence Survey Self-efficacy will be assessed by the Exercise Confidence Survey. This measure will be used to assess the various components of Social Cognitive Theory which are guiding the TeleSalud HE-PA/SB intervention. Baseline, 4 months, 8 months
Secondary Social Support and Eating Habits Survey Social Support will be assessed by the Social Support and Exercise Survey and the Social Support and Eating Habits Survey. These measures will be used to assess the various components of Social Cognitive Theory which are guiding the TeleSalud HE-PA/SB intervention. Baseline, 4 months, 8 months
Secondary Social Support and Exercise Survey Social Support will be assessed by the Social Support and Exercise Survey and the Social Support and Eating Habits Survey. These measures will be used to assess the various components of Social Cognitive Theory which are guiding the TeleSalud HE-PA/SB intervention. Baseline, 4 months, 8 months
See also
  Status Clinical Trial Phase
Recruiting NCT04243317 - Feasibility of a Sleep Improvement Intervention for Weight Loss and Its Maintenance in Sleep Impaired Obese Adults N/A
Recruiting NCT04101669 - EndoBarrier System Pivotal Trial(Rev E v2) N/A
Terminated NCT03772886 - Reducing Cesarean Delivery Rate in Obese Patients Using the Peanut Ball N/A
Completed NCT03640442 - Modified Ramped Position for Intubation of Obese Females. N/A
Completed NCT04506996 - Monday-Focused Tailored Rapid Interactive Mobile Messaging for Weight Management 2 N/A
Recruiting NCT06019832 - Analysis of Stem and Non-Stem Tibial Component N/A
Active, not recruiting NCT05891834 - Study of INV-202 in Patients With Obesity and Metabolic Syndrome Phase 2
Active, not recruiting NCT05275959 - Beijing (Peking)---Myopia and Obesity Comorbidity Intervention (BMOCI) N/A
Recruiting NCT04575194 - Study of the Cardiometabolic Effects of Obesity Pharmacotherapy Phase 4
Completed NCT04513769 - Nutritious Eating With Soul at Rare Variety Cafe N/A
Withdrawn NCT03042897 - Exercise and Diet Intervention in Promoting Weight Loss in Obese Patients With Stage I Endometrial Cancer N/A
Completed NCT03644524 - Heat Therapy and Cardiometabolic Health in Obese Women N/A
Recruiting NCT05917873 - Metabolic Effects of Four-week Lactate-ketone Ester Supplementation N/A
Active, not recruiting NCT04353258 - Research Intervention to Support Healthy Eating and Exercise N/A
Completed NCT04507867 - Effect of a NSS to Reduce Complications in Patients With Covid-19 and Comorbidities in Stage III N/A
Recruiting NCT03227575 - Effects of Brisk Walking and Regular Intensity Exercise Interventions on Glycemic Control N/A
Completed NCT01870947 - Assisted Exercise in Obese Endometrial Cancer Patients N/A
Recruiting NCT05972564 - The Effect of SGLT2 Inhibition on Adipose Inflammation and Endothelial Function Phase 1/Phase 2
Recruiting NCT06007404 - Understanding Metabolism and Inflammation Risks for Diabetes in Adolescents
Recruiting NCT05371496 - Cardiac and Metabolic Effects of Semaglutide in Heart Failure With Preserved Ejection Fraction Phase 2