Remotely Delivered Resistance Training for Cardiometabolic Health Among Black Women
- Conditions
- Overweight or ObesityPrediabetes or DiabetesPrehypertension (Elevated Blood Pressure) or HypertensionResistance Training
- Interventions
- Behavioral: Resistance Training
- Registration Number
- NCT06360536
- Lead Sponsor
- University of Alabama at Birmingham
- Brief 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.
- Detailed 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.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- Female
- Target Recruitment
- 36
- Self-identifies as Black or African American
- Female
- Age 30-64 years
- Insufficient resistance training engagement (<2 sessions/week in the past 6 months)
AND
- Self-reported or documented diagnosis of at least one of the following conditions: Overweight, obesity, prediabetes, type 2 diabetes, elevated blood pressure, hypertension, or taking medications for any of these conditions
- Has an internet- connected device (i.e., computer, smartphone) and is willing to use it for intervention delivery
- If indicated during screening, willing to obtain medical clearance for exercise from their healthcare provider prior to enrollment
- Residing within a 50-mile radius of the University
- Uncontrolled hypertension (blood pressure >160/100 mm Hg)
- Weighing ≥ 450 lbs (upper limit for body composition assessment)
- Conditions or limitations that affect physical activity participation and/or the ability to --perform assessments
- Has a medical or physical condition that make moderate intensity physical activity (like a brisk walk) difficult or unsafe
- Unwilling to obtain medical clearance (if indicated by prescreening)
- Women who are pregnant or trying to become pregnant in the next 6 months
- Planning to relocate out of the area in the next 6 months
- Participating in another exercise and/or randomized research project
- Unwilling or unable to do any of the following: give informed consent; read/understand English; perform resistance training in their home, record and upload virtual exercise assessment sessions, and other protocol specific requirements
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Intervention/Treatment Resistance Training A home-based resistance training condition that is delivered through a web-based platform.
- Primary Outcome Measures
Name Time Method Feasibility of recruitment Baseline The number of participants enrolled in the trial
Feasibility of retention Month 4 The proportion of participants who complete the study out of those who enrolled in the study
Intervention adherence Month 4 The number of participants adhering to the intervention
- Secondary Outcome Measures
Name Time Method Change in HbA1C Baseline, Month 4 HbA1C measured by a point-of-care device
Change in resistance training behaviors Baseline and Month 4 The number of days of resistance training completed
Change in blood pressure Baseline, Month 4 Systolic and diastolic blood pressure measured by an automated device
Change in body composition Baseline, Month 4 Percent body fat measured by dual-energy x-ray absorptiometry
Change in handgrip strength Baseline, Month 4 The highest value of 3 maximal attempts on each hand
Change in the number of chair stands Baseline, Month 4 The number of chair stands completed in 30 seconds
Trial Locations
- Locations (1)
University of Alabama at Birmingham
🇺🇸Birmingham, Alabama, United States