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Pilot Social Network Weight Loss Intervention (HIC)

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Mayo Clinic

Status

Completed

Conditions

Weight Loss
Diet, Healthy

Treatments

Behavioral: Mentoring/educational session

Study type

Interventional

Funder types

Other

Identifiers

NCT04273503
19-011574

Details and patient eligibility

About

Specific Aim #1: Pilot test a social network-informed CBPR-derived health promotion program for feasibility outcomes with overweight or obese adults from two immigrant communities.

Specific Aim #2: Assess the preliminary impact of embedding a social network-informed CBPR-derived intervention within a regional health promotion resource hub on sustainability and uptake outcomes.

Full description

The intervention will consist of 12 community-based mentoring and education sessions, group activities and application of a community toolkit for healthy weight loss delivered by trained interventionists from Hispanic and Somali communities to their social networks. Using a pre-post study design, 4 social networks of adults with approximately 32 network participants will receive the intervention. Primary outcomes, measured 3 months after implementation, will include feasibility measures of acceptability, implementation, and practicality. Secondary outcomes will include BMI, waist circumference, blood pressure, fasting blood glucose, total cholesterol, physical activity level, dietary change, and health-related quality of life.

Eligibility criteria include (1) self-identification as Hispanic or Somali, (2) member of an HPs social network, (3) age≥18 and <65 (4) willingness to participate in all aspects of the study; and (5) provision of informed consent. Exclusion criteria include (1) pregnancy at the time of enrollment and (2) serious medical conditions or disabilities that would make physical activity difficult.

We will test how best to integrate a social network intervention within an existing evidence-based regional health promotion infrastructure (WellConnect) that will enhance its potential dissemination and community-wide uptake

Enrollment

39 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. self-identification as Hispanic or Somali
  2. member of an HPs social network
  3. age≥18 and <65
  4. willingness to participate in all aspects of the study
  5. provision of informed consent.

Exclusion criteria

  1. pregnancy at the time of enrollment

  2. serious medical conditions or disabilities that would make physical activity difficult.

    • To avoid stigmatization, a normal weight (BMI<25) will not exclude individuals from participating, but they will be excluded from the measurements and analyses.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

39 participants in 1 patient group

Intervention
Experimental group
Description:
All participants will receive education on maintaining a healthy diet and improving physical activity.
Treatment:
Behavioral: Mentoring/educational session

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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