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NCT06340503Completed

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

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

Source: ClinicalTrials.gov · Last updated 29 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
25 Mar 2024
Start date
6 Nov 2024
Primary completion date
8 Jun 2026
Lead sponsor
Wake Forest University Health Sciences
NCT number
NCT06340503

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 6 Nov 2024 to the primary completion date, 8 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants receiving treatment other than maintenance therapy for their primary cancer (breast or colon).
  • Participants has prior conditions that contraindicate exercise as determined by treating physician.

Other illness

  • Participants with metastatic disease.
  • Participants with recurrence or diagnosis of a different cancer.
  • Participants has gross cognitive impairment as determined by treating physician.

Who the study is looking for

  • Survivors of breast or colon cancer (stages 0-III) diagnosed within the last three years prior to enrollment.
  • Completed primary treatment (surgery, chemotherapy, and/or radiation) at least 3 months prior to enrollment.
  • At least 50 years of age or older.
  • Access to internet or cellular plan for video calls.
  • 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.
  • Able to read and speak English

Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Atrium Health Wake Forest Baptist Comprehensive Cancer Center
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.