Clinical trial · Interventional
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
NCT06340503CI-TRIAL-00116227completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Colon Cancer | Malignant Colon Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (8)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Exercise Consultation Calls | Other | — | UNRESOLVED |
| Garmin Vivofit activity tracker | Device | — | UNRESOLVED |
| Health Surveys | Other | — | UNRESOLVED |
| Interview | Other | — | UNRESOLVED |
| National Comprehensive Cancer Network (NCCN) Education Materials | Other | — | UNRESOLVED |
| Physical Activity Index Assessment (Control Arm) | Other | — | UNRESOLVED |
| Physical Activity Index Assessment (Intervention Arm) | Other | — | UNRESOLVED |
| Research-grade accelerometer | Device | — |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Exercise Group
- description
- Participants randomized into the exercise group will receive a pre-exercise screening call about two weeks after enrolling into the study and complete the six (6) study visits and pre-determined test and procedures for the patient intervention arm.
- interventionNames
- Device: Research-grade accelerometer
- Other: National Comprehensive Cancer Network (NCCN) Education Materials
- Device: Garmin Vivofit activity tracker
- Other: Exercise Consultation Calls
- Other: Interview
- Other: Physical Activity Index Assessment (Intervention Arm)
- Other: Health Surveys
- type
- ACTIVE_COMPARATOR
- label
- Delayed Exercise Group
- description
- Participants randomized to the delayed exercise group, will have vitals collected and complete surveys at the first (baseline), 3-month, and 6-month visits pre-determined test and procedures for the waitlist control arm. The pre-exercise consultation will begin after the 6-month visit.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 50 Years
Show eligibility criteria text
Inclusion Criteria: * 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 Exclusion Criteria: * Participants with metastatic disease. * Participants with recurrence or diagnosis of a different cancer. * 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. * Participants has gross cognitive impairment as determined by treating physician.
References
Publications (0)
Data not yet available
No reference posted for this study.