Obesity Clinical Trial
Official title:
Puerto Rican Obesity Intervention for Men
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.
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. |
Country | Name | City | State |
---|---|---|---|
United States | Medical College of Wisconsin | Milwaukee | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
Medical College of Wisconsin |
United States,
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 |
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