ClinicalTrials.Veeva

Menu

Remotely Delivered Resistance Training for Cardiometabolic Health Among Black Women (OVERCOME-IT)

The University of Alabama at Birmingham logo

The University of Alabama at Birmingham

Status

Enrolling

Conditions

Prediabetes or Diabetes
Prehypertension (Elevated Blood Pressure) or Hypertension
Overweight or Obesity
Resistance Training

Treatments

Behavioral: Resistance Training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06360536
IRB-300012634
P50MD017338 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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.

Enrollment

36 estimated patients

Sex

Female

Ages

30 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

36 participants in 1 patient group

Intervention/Treatment
Experimental group
Description:
A home-based resistance training condition that is delivered through a web-based platform.
Treatment:
Behavioral: Resistance Training

Trial contacts and locations

1

Loading...

Central trial contact

Sarahi Hernandez, MPH

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems