Designing a Dyad-Based mHealth Intervention to Improve Adherence to Lifestyle Recommendations in Colorectal Cancer Survivors and Their Family Caregivers

NCT06746012 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2026-04-09

No results posted yet for this study

Summary

This clinical trial develops and tests a mobile health (mHealth) intervention to improve adherence to lifestyle recommendations in colorectal cancer (CRC) survivors and their family caregivers. The current challenge for cancer survivorship is identifying novel approaches to help adhere to the lifestyle recommendations that have been shown to improve symptom burden, health outcomes, and health-related quality of life (HRQoL). The development of a digital health intervention specifically for CRC survivors and family caregivers may improve adherence to the American Cancer Society Nutrition and Physical Activity Guideline for Cancer Survivors and improve family health.

Conditions

  • Stage I Colon Cancer AJCC v8
  • Stage I Rectal Cancer AJCC v8
  • Stage II Colon Cancer AJCC v8
  • Stage II Rectal Cancer AJCC v8
  • Stage III Colon Cancer AJCC v8
  • Stage III Rectal Cancer AJCC v8

Interventions

PROCEDURE

Discussion

Participate in think-aloud sessions

OTHER

Educational Activity

Receive health coaching

OTHER

Internet-Based Intervention

Use Healthy Buckeyes app

OTHER

Internet-Based Intervention

Watch videos

OTHER

Interview

Complete semi-structured interview

OTHER

Medical Device Usage and Evaluation

Wear Fitbiit and use exercise bands

OTHER

Questionnaire Administration

Ancillary studies

OTHER

Supportive Care

Receive caregiver support

OTHER

Survey Administration

Complete surveys

Sponsors & Collaborators

  • Ohio State University Comprehensive Cancer Center

    lead OTHER

Principal Investigators

  • Roberto M Benzo, PhD · Ohio State University Comprehensive Cancer Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-05-03
Primary Completion
2026-12-31
Completion
2026-12-31

Countries

  • United States

Study Locations

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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 NCT06746012 on ClinicalTrials.gov