Clinical trial

Remotely Delivered Resistance Training for Cardiometabolic Health Among Black Women

Active, not recruiting · Not applicable · 1 countries · Registry ID NCT06360536

Active, not recruitingNot applicableInterventional

What this study is 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.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age30 Years to 64 Years
SexFemale
Healthy volunteersNot accepted
ConditionOverweight or Obesity, Prediabetes or Diabetes, Prehypertension (Elevated Blood Pressure) or Hypertension, Resistance Training

Full registry criteria

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

Treatments and study arms

Resistance Training

Behavioral

A home-based resistance training condition that is delivered through a web-based platform.

Primary outcomes

Feasibility of recruitmentBaseline

The number of participants enrolled in the trial

Feasibility of retentionMonth 4

The proportion of participants who complete the study out of those who enrolled in the study

Intervention adherenceMonth 4

The number of participants adhering to the intervention

Study locations

1 locations were listed when this page was built. The first 40 are shown.

University of Alabama at Birmingham🇺🇸 Birmingham, Alabama, United States