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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05544708
Other study ID # HM20024014
Secondary ID 1R01DK132373
Status Recruiting
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date March 1, 2025

Study information

Verified date May 2024
Source Virginia Commonwealth University
Contact Morgan Meyer
Phone (804) 827-2250
Email morgan.meyer@vcuhealth.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date March 1, 2025
Est. primary completion date November 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Wellness Engagement Intervention
Train for, recruit participants into, and lead a 12-week lifestyle intervention delivered via weekly group meetings

Locations

Country Name City State
United States Virginia Commonwealth University Richmond Virginia

Sponsors (2)

Lead Sponsor Collaborator
Virginia Commonwealth University National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility: House Chat Leaders (HCL) The number of house chat leaders successfully recruited, trained, and retained. 18 months
Primary Feasibility: Participants The average number of participants recruited by the HCLs. 18 months
Primary Feasibility: Delivery Model The number of intervention sessions delivered; the number of planned session topics that were covered 12 weeks
Secondary Acceptability: Attendance The average number of sessions attended by participants. 12 weeks
Secondary Acceptability: Retention The average number of HCL and participants who are retained in the program 12 weeks
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