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Making Healthy Habits Stick

NCT06745180 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 260

Last updated 2025-10-01

No results posted yet for this study

Summary

The aim of this project is to help increase physical activity maintenance in cancer survivors.

Conditions

  • Cancer
  • Physical Activity
  • Cancer Survivor
  • Cancer Survivorship

Interventions

BEHAVIORAL

Short Message System (SMS)

The Short Message System (SMS) intervention focuses on personalized, adaptive SMS messages that help the participant maintain physical activity behaviors.

BEHAVIORAL

Peer Coach

The peer coach will deliver an intervention that will help participants maintain physical activity.

BEHAVIORAL

Usual Care

Participants will be given written materials providing advice on maintaining their physical activity.

BEHAVIORAL

Peer Coach and SMS

The Short Message System (SMS) intervention focuses on personalized, adaptive SMS messages that help the participant maintain physical activity behaviors. The peer coach will deliver an intervention that will help participants maintain physical activity.

Sponsors & Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)

    collaborator NIH

  • University of Alabama at Birmingham

    collaborator OTHER

  • University of Tennessee

    lead OTHER

Principal Investigators

  • Michelle Martin, PhD · University of Tennessee

  • Laura Rogers, MD, MPH · University of Alabama at Birmingham

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
FACTORIAL

Eligibility

Min Age
19 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-27
Primary Completion
2028-03-31
Completion
2028-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06745180 on ClinicalTrials.gov