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Texts and peers aim to keep cancer survivors moving

NCT ID NCT06745180

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 personalized text messages and support from a peer coach can help Black female cancer survivors keep up a regular exercise routine after treatment. Researchers will enroll 260 women and track their physical activity, fatigue, and quality of life. The goal is to find simple, lasting ways to promote healthy habits in this group.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
SMS text messages and peer coaching
What this could lead to
If successful, this could provide a simple, low-cost way to help cancer survivors maintain physical activity, improving their health and quality of life.
What could go wrong
This is a behavioral study with no drug or medical treatment. Results depend on participants' motivation and may not apply to other groups. The trial is still recruiting, so outcomes are uncertain.

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

About 260 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2025

Expected to finish

Mar 2028

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

19 years and older

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: * woman age of 19 or older * identifies as African American or Black * have a history of cancer * have completed post-primary treatment for cancer (i.e., chemotherapy, radiation) * agree to allow research team to confirm cancer diagnosis with your physician * If received surgery, must be at least 8 weeks post-surgery * willing to have regular physician provide medical clearance for study participation * willing to provide home address if qualified for the study * willing and able to use videoconference platform such as Zoom for study activities (must be both willing and able) * willing and able to send and/or receive text messages (must be both willing and able) * has US phone number * has an email address * if has no email address, must be willing to create one * English speaking * Able to ambulate without assistance (does not need to use a cane, a walker, or a wheelchair) * willing and able to complete 3-5 exercise session per week on their own for the duration of the study; if answered no, please explain * willing to attend individual and group sessions via videoconferences during study participation; if answered no, please explain. * willing to attend assessments via videoconference during study participation; if answered no, please explain. * willing to complete surveys during study participation; if answered no, please explain. Exclusion Criteria: * Metastatic or recurrent cancer * another cancer diagnosis in the past 5 years (not including skin or cervical cancer in situ) * have severe orthopedic, joints or any other condition that stops individual from being active * unstable angina * have paint, tightness, or heaviness in chest EITHER when resting OR then physically active * have New York Heart Association class II, III, OR IV congestive heart failure * blood pressure has been over 160/100 at least twice in the past 6 months (either number; 160 or 100) * have uncontrolled asthma * have interstitial lung disease that requires extra oxygen * have dementia or organize brain syndrome * have schizophrenia or active psychosis * have had a stroke or other problem that left individual disables or with paralysis (unable to move or feel any part of body) * have hearing problems that make it hard to carry on a phone conversation * blind or partially blind * planned surgery during the first 6 month of study participation (if unapproved by PI) * planned knee or hip surgery during the first 6 month of study participation * anticipate changes in usual medications during the first 6 months of study participation (if unapproved by PI) * have been told by a physician to only do exercise prescribed by a physician * have been told by a physician to limit physical activity * have a contraindication to engaging in moderate intensity aerobic exercise * have completed on average, more than 90 min/week of moderate-intensity or more that 30 min/week of vigorous exercise in the past 6 months * trouble with balance or moving around safely * are currently pregnant or anticipate pregnant during study participation * currently participating in another exercise study * have BMI ≥ 50

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Conditions

The condition(s) this trial relates to.

cancer Motor Activity neoplasm

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • University of Alabama at Birmingham

    RECRUITING

    Birmingham, Alabama, 35294, United States

  • University of Tennessee Health Science Center

    RECRUITING

    Memphis, Tennessee, 38163, United States

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