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Using Grassroots Wellness Coaching to Enhance Reach and Sustainability of Behavioral Weight Management

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Completed

Conditions

Obesity

Treatments

Behavioral: Wellness Engagement Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05544708
HM20024014
1R01DK132373 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

African American adults that live in economically disadvantaged areas are at an increased risk for obesity and cardiometabolic disease. The treatment program being tested in this research study aims to address these factors and increase outcomes for the study population. The purpose of this research study is to find out about the feasibility and acceptability of using house chats (HC) as a model for a weight loss program in a real-world, community-based setting.

Enrollment

71 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18 and older
  • Resident of Petersburg, VA
  • Interested in engaging community members in healthy lifestyle changes (e.g., walking, small changes to eating) and willing to engage in these behaviors her/himself

Exclusion criteria

  • A diagnosis of type 1 diabetes mellitus.
  • Currently being treated for cancer.
  • Medical conditions that may increase risk for participating in unsupervised exercise, if medical clearance is not provided
  • Hospitalization for depression or other psychiatric disorder within the past 12 months.
  • Lifetime history of bipolar disorder or psychotic disorder.
  • Currently pregnant or lactating, or planning to become pregnant within the study period.
  • Current involvement in a weight loss program or current use of weight loss medication.
  • Inability to speak, read and write English.
  • Planning to move from the Petersburg area within the study period.
  • Does not have sufficient numbers of individuals in their social network from which to recruit for the proposed study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

71 participants in 2 patient groups

Intervention
Experimental group
Description:
Wellness Ambassadors will undergo training to recruit and deliver a lifestyle intervention to members of their social networks. HCL in the intervention group will deliver the intervention immediately following baseline visits and randomization.
Treatment:
Behavioral: Wellness Engagement Intervention
Delayed Intervention
No Intervention group
Description:
Wellness Ambassadors will undergo training to recruit and deliver a lifestyle intervention to members of their social networks. HCL in the delayed intervention group will deliver the intervention after 24 week data collection visits are complete.

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Morgan Meyer

Data sourced from clinicaltrials.gov

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