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Clinical Trial Summary

The purpose of this study is to collect preliminary data on the feasibility, acceptability, and potential effects of a novel, remotely delivered resistance training program.


Clinical Trial Description

This trial will enroll Black women with elevated cardiometabolic risk (e.g., overweight or obesity, pre- or established diabetes, and elevated or high blood pressure) in early-to-middle adulthood (n=36; age=30-64 years) with insufficient resistance training (RT) participation. This 4-month single group pilot trial evaluates the feasibility, acceptability, and potential effects of a novel, remotely-delivered resistance training (RT) intervention. All participants will engage in RT during this trial and the web-based platform is the primary modality through which the remote RT intervention is delivered. Assessments are conducted at baseline and follow-up (month 4). Aim 1 will examine the feasibility and acceptability of the remotely delivered RT program. Aim 2 will examine the potential effects on RT behaviors. Aim 3 will examine the potential effects on clinical and patient-reported outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06360536
Study type Interventional
Source University of Alabama at Birmingham
Contact Jackie Grant
Phone 205-975-7108
Email jroche@uabmc.edu
Status Not yet recruiting
Phase N/A
Start date September 1, 2024
Completion date June 30, 2026

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