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Home workout study aims to boost heart health in black women

NCT ID NCT06360536

Knowledge-focused Sponsor: University of Alabama at Birmingham Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a remotely delivered resistance training program is practical and helpful for Black women aged 30-64 who are overweight, have prediabetes or diabetes, or have high blood pressure. About 37 women will participate from home using their own devices. The goal is to see if the program is easy to follow and if it leads to improvements in blood pressure, blood sugar, and body composition.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

37 people

The number who actually took part.

Started

Mar 2026

Expected to finish

Jun 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 to 64 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

diabetes mellitus hypertensive disorder Obesity obesity disorder Overweight prediabetes syndrome Prehypertension type 2 diabetes mellitus

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Overweight or obesity Prediabetes or diabetes Prehypertension (elevated blood pressure) or hypertension Resistance training

Contacts and locations

Locations

  • University of Alabama at Birmingham

    Birmingham, Alabama, 35294, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.