ACTIVE_NOT_RECRUITING

Evaluating a Physical Activity Index for Assessment and Counseling for Breast and Colon Cancer Survivors

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 research study is to determine whether using the physical activity index screener, exercise coaching, and self-monitoring will increase physical activity and reduce time spent sitting or being inactive in patients who had breast or colon cancer.

Official Title

Evaluating a Physical Activity Index for Assessment and Counseling for Breast and Colon Cancer Survivors in Clinical Practice

Quick Facts

Study Start:2024-11-06
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06340503

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:50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Survivors of breast or colon cancer (stages 0-III) diagnosed within the last three years prior to enrollment.
  2. * Completed primary treatment (surgery, chemotherapy, and/or radiation) at least 3 months prior to enrollment.
  3. * At least 50 years of age or older.
  4. * Access to internet or cellular plan for video calls.
  5. * Being willing and able to comply with the approved protocol and able to sign an IRB-approved informed consent document directly, remotely or via electronic consent.
  6. * Able to read and speak English
  1. * Participants with metastatic disease.
  2. * Participants with recurrence or diagnosis of a different cancer.
  3. * Participants receiving treatment other than maintenance therapy for their primary cancer (breast or colon).
  4. * Participants has prior conditions that contraindicate exercise as determined by treating physician.
  5. * Participants has gross cognitive impairment as determined by treating physician.

Contacts and Locations

Principal Investigator

Shirley Bluethmann
PRINCIPAL_INVESTIGATOR
Wake Forest Baptist Comprehensive Cancer Center

Study Locations (Sites)

Atrium Health Wake Forest Baptist Comprehensive Cancer Center
Winston-Salem, North Carolina, 27157
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

  • Shirley Bluethmann, PRINCIPAL_INVESTIGATOR, Wake Forest Baptist Comprehensive Cancer Center

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 Date2024-11-06
Study Completion Date2026-06

Study Record Updates

Study Start Date2024-11-06
Study Completion Date2026-06

Terms related to this study

Keywords Provided by Researchers

  • Physical activity
  • Exercise coaching

Additional Relevant MeSH Terms

  • Breast Cancer
  • Colon Cancer