Puerto Rican Obesity Intervention for Men

April 27, 2026 updated by: Lisa Sanchez-Johnsen, Medical College of Wisconsin

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.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

48

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria:

  1. Male of Puerto Rican descent over 35 years.
  2. BMI ≥25 by anthropometrically measured weight and height.
  3. Physically able to exercise (via the EASY tool [106, 107]; Appendix 2). If responses to the EASY indicate that medical clearance is needed, then able to receive medical clearance to participate in the study.
  4. Has access to secure computer or tablet in a private location with reliable internet connection to support video streaming
  5. Ability to understand and speak English. For those without a high-speed internet and private space to exercise, we will work with our community partners to identify a space with access to videoconferencing so they can attend the telehealth class.

Exclusion:

  1. Does not understand/speak English.
  2. Plans to move from the Illinois or Wisconsin area during the study.
  3. Currently in a formal weight management program.
  4. Current or planned use of weight control or loss medication prescribed by a doctor.
  5. Currently exercising >1 time/week.
  6. Unable to attend study times.
  7. 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). Patients who have been treated for cancer in the past 5 years may require different diet and PA recommendations than individuals without treatment for cancer in the past 5 years.
  8. In the EASY interview, if participant answers yes to the question that indicates they fall or always use an assisted device while walking.
  9. Current alcohol abuse (>35 alcoholic drinks/week); score of yes to > 2 questions on the CAGE alcohol scale (Appendix 1) [108].

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Healthy Eating and Physical Activity - Intervention
Participants will attend virtual classes on increasing healthy eating, increasing physical activity, and decreasing sedentary behaviors.
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.
Active Comparator: General Health Topics - Control
Participants will attend virtual classes on general health topics.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Acceptability- Fidelity: Delivery
Time Frame: 4 months, 8 months
Delivery will be measured by an adherence checklist. It will monitor consistency and accuracy in the delivery of the intervention.
4 months, 8 months
Acceptability- Fidelity: Receipt
Time Frame: 4 months, 8 months
Receipt will be measured by participants' self-reports of understanding and knowledge acquisition of content for both groups.
4 months, 8 months
Acceptability- Fidelity: Enactment
Time Frame: 4 months, 8 months
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
Acceptability- Helpfulness of Treatment Components
Time Frame: 4 months, 8 months
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
Acceptability- Helpfulness/ Effectiveness of the Intervention Leaders
Time Frame: 4 months, 8 months
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
Acceptability- Intervention Satisfaction
Time Frame: 4 months, 8 months
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
Acceptability- Perceived Helpfulness/ Effectiveness of the Telehealth Modality, Technology, and Equipment
Time Frame: Baseline, 4 months, 8 months
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
Acceptability- Satisfaction with Random Assignment to Groups
Time Frame: Baseline, 4 months, 8 months
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
Dietary Intake: Number of Servings of Fruits
Time Frame: Baseline, 4 months, 8 months
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
Dietary Intake: Number of Servings of Vegetables
Time Frame: Baseline, 4 months, 8 months
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
Dietary Intake: Percent of Calories from Saturated Fat
Time Frame: Baseline, 4 months, 8 months
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
Dietary Intake: Total Energy Intake
Time Frame: Baseline, 4 months, 8 months
Changes in total energy intake will be measured by the Automated Self-Administered 24-Hour (ASA24) Dietary Assessment Tool.
Baseline, 4 months, 8 months
Feasibility- Adherence- Monthly Attendance
Time Frame: 4 months, 8 months
Feasibility- Adherence- Monthly: Will be measured by the frequency of attendance at each session on a monthly basis.
4 months, 8 months
Feasibility- Adherence- Number of Make-Up Sessions
Time Frame: 4 months, 8 months
Feasibility- Adherence- Number of Make-Up Sessions: Will be assessed by frequency/counts of number of make-up sessions.
4 months, 8 months
Feasibility- Adherence- Number of Missed Sessions Overall
Time Frame: 4 months, 8 months
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
Feasibility- Adherence- Weekly Attendance
Time Frame: 4 months, 8 months
Feasibility- Adherence- Weekly Attendance: Will be measured by the frequency of attendance at each session on a weekly basis.
4 months, 8 months
Feasibility- Recruitment- Number Enrolled
Time Frame: Pre-Intervention
Recruitment feasibility assessed by the number of participants enrolled.
Pre-Intervention
Feasibility- Recruitment- Number of Contacts
Time Frame: Pre-Intervention
Recruitment feasibility assessed by counts of the number of contacts.
Pre-Intervention
Feasibility- Recruitment- Rate of Consenting
Time Frame: Pre-Intervention
Recruitment feasibility assessed by the rate of consenting.
Pre-Intervention
Feasibility- Recruitment- Rate of Enrollment
Time Frame: Pre-Intervention
Recruitment feasibility assessed by the rate of enrollment.
Pre-Intervention
Feasibility- Recruitment- Rate of Screening
Time Frame: Pre-Intervention
Recruitment feasibility assessed by the rate of screening.
Pre-Intervention
Feasibility- Recruitment- Recruitment Method
Time Frame: Pre-Intervention
Feasibility assessed by tracking the method of recruitment.
Pre-Intervention
Feasibility- Recruitment- Response Rate
Time Frame: Pre-Intervention
Recruitment feasibility assessed by rate of response.
Pre-Intervention
Feasibility- Recruitment- Type of Contact
Time Frame: Pre-Intervention
Recruitment feasibility assessed by tracking the type of contact.
Pre-Intervention
Feasibility- Retention- Number Completed the intervention
Time Frame: 4 months, 8 months
Retention assessed by counts and frequency of the number who completed the interventions.
4 months, 8 months
Feasibility- Recruitment- Number Screened
Time Frame: Pre-Intervention
Recruitment feasibility assessed by the count of number of individuals screened.
Pre-Intervention
Feasibility- Retention- Number of Classes Attended
Time Frame: 4 months, 8 months
Retention- assessed by counts of the number of classes attended.
4 months, 8 months
Feasibility- Retention- Percent Completed the Interventions
Time Frame: 4 months, 8 months
Retention assessed by the percent of participants who completed the interventions.
4 months, 8 months
Feasibility- Retention- Percent of Classes Attended
Time Frame: 4 months, 8 months
Retention assessed by percent of classes attended.
4 months, 8 months
Feasibility- Recruitment- Number Consented
Time Frame: Pre-Intervention
Recruitment feasibility assessed by the number of participants who consented.
Pre-Intervention
Objective Physical Activity (Accelerometer)
Time Frame: Baseline, 4 months, 8 months
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
Subjective Physical Activity (International Physical Activity Questionnaire)
Time Frame: Baseline, 4 months, 8 months
The International Physical Activity Questionnaire long form- will measure sedentary and leisure and non-leisure time physical activity.
Baseline, 4 months, 8 months
Subjective Sedentary Behavior (International Physical Activity Questionnaire)
Time Frame: Baseline, 4 months, 8 months
The International Physical Activity Questionnaire long form- will measure sedentary and leisure and non-leisure time physical activity.
Baseline, 4 months, 8 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body Mass Index
Time Frame: Baseline, 4 months, 8 months
Body Mass Index (BMI) will be assessed by objectively measured height and weight.
Baseline, 4 months, 8 months
Outcome Expectations for Diet Questionnaire
Time Frame: Baseline, 4 months, 8 months
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
Exercise Outcomes on the Outcomes Expectations Questionnaire
Time Frame: Baseline, 4 months, 8 months
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
Self-Efficacy for Dietary Behaviors
Time Frame: Baseline, 4 months, 8 months
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
Exercise Confidence Survey
Time Frame: Baseline, 4 months, 8 months
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
Social Support and Eating Habits Survey
Time Frame: Baseline, 4 months, 8 months
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
Social Support and Exercise Survey
Time Frame: Baseline, 4 months, 8 months
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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lisa Sanchez-Johnsen, PhD, Medical College of Wisconsin

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

May 31, 2027

Study Completion (Estimated)

August 31, 2027

Study Registration Dates

First Submitted

April 26, 2024

First Submitted That Met QC Criteria

May 31, 2024

First Posted (Actual)

June 4, 2024

Study Record Updates

Last Update Posted (Actual)

May 1, 2026

Last Update Submitted That Met QC Criteria

April 27, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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