RECRUITING

Remotely Delivered Resistance Training for Cardiometabolic Health Among Black Women

Conditions

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

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Remotely Delivered Resistance Training for Cardiometabolic Health Among Black Women: A Pilot Trial

Quick Facts

Study Start:2025-06-04

Study Completion:2026-06-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06360536

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:30 Years to 64 Years

Sexes Eligible for Study:FEMALE

Accepts Healthy Volunteers:No

Standard Ages:ADULT

Inclusion Criteria	Exclusion 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) * 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

Inclusion Criteria

Exclusion 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)
* 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

Contacts and Locations

Study Contact

Sarahi Hernandez, MPH

CONTACT

205-996-1638

sarahihernandez@uabmc.edu

Principal Investigator

Amber W Kinsey, PhD

PRINCIPAL_INVESTIGATOR

University of Alabama at Birmingham

Study Locations (Sites)

University of Alabama at Birmingham

Birmingham, Alabama, 35294

United States

Collaborators and Investigators

Sponsor: University of Alabama at Birmingham

Amber W Kinsey, PhD, PRINCIPAL_INVESTIGATOR, University of Alabama at Birmingham

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-06-04

Study Completion Date2026-06-30

Study Record Updates

Study Start Date2025-06-04

Study Completion Date2026-06-30

Terms related to this study

Additional Relevant MeSH Terms

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