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Community-Based Mentoring for Weight Loss
N/A
Waitlist Available
Led By Mark Wieland, MD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 6 months, 12 months, 24 months
Awards & highlights
No Placebo-Only Group
Summary
This trial will use social networks to try and change health behaviors in people that are at risk for obesity and heart problems.
Who is the study for?
This trial is for Hispanic or Somali immigrants in Southeast Minnesota who are willing to fully participate and consent. It's aimed at those with obesity or cardiovascular risk factors, but excludes pregnant individuals, those with serious conditions limiting physical activity, and normal-weight people from measurements.
What is being tested?
The study tests a program using community-based mentoring and education within social networks to promote weight loss and reduce cardiovascular risks among immigrant communities.
What are the potential side effects?
Since the intervention involves lifestyle changes through mentoring and education sessions rather than medication, typical drug side effects aren't expected. However, participants may experience stress or time constraints due to participation.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 6 months, 12 months, 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 6 months, 12 months, 24 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Body Mass Index (BMI)
Change in waist circumference
Secondary study objectives
Change in "Life's Simple 7" Composite Score
Change in Dietary Quality
Change in blood pressure (systolic and diastolic)
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Immediate Community-Based Mentoring and Education SessionsExperimental Treatment1 Intervention
Subjects will receive the intervention of community-based mentoring and education sessions immediately after enrollment.
Group II: Delayed Community-Based Mentoring and Education SessionsExperimental Treatment1 Intervention
Subjects will receive the intervention of community-based mentoring and education sessions approximately 12 months after enrollment.
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Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,362 Previous Clinical Trials
3,065,480 Total Patients Enrolled
18 Trials studying Weight Loss
738 Patients Enrolled for Weight Loss
National Institute on Minority Health and Health Disparities (NIMHD)NIH
444 Previous Clinical Trials
1,413,030 Total Patients Enrolled
6 Trials studying Weight Loss
1,175 Patients Enrolled for Weight Loss
Mark Wieland, MDPrincipal InvestigatorMayo Clinic
2 Previous Clinical Trials
93 Total Patients Enrolled
1 Trials studying Weight Loss
39 Patients Enrolled for Weight Loss
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are part of a social group that was identified in a network analysis.The participants in the study were willing to take part in all aspects of the research.I have a condition that makes it hard for me to be physically active.Even if you are not overweight, you can still participate in the study, but you will not be included in the measurements and analysis.You identify yourself as Hispanic or Somali.
Research Study Groups:
This trial has the following groups:- Group 1: Immediate Community-Based Mentoring and Education Sessions
- Group 2: Delayed Community-Based Mentoring and Education Sessions
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.