Physical Activity and Healthy Eating Among Young Adult Cancer Survivors

NCT05887401 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2025-12-24

Study results available
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Summary

The purpose of this pilot randomized factorial trial is to test the feasibility, acceptability, and effects of a theory-based mobile physical activity and nutrition intervention designed specifically for young adult cancer survivors to increase physical activity and diet quality.

Conditions

  • Physical Activity
  • Neoplasms
  • Cancer

Interventions

BEHAVIORAL

Core Intervention

The core intervention will include behavioral lessons, activity tracker, weekly adaptive physical activity goals, weekly tailored feedback summary.

BEHAVIORAL

Simplified Dietary Monitoring (Green)

Simplified diet monitoring using smartphone tracking of green foods using a traffic light approach.

BEHAVIORAL

Simplified Dietary Monitoring (Red)

Simplified diet monitoring using smartphone tracking of red foods using a traffic light approach.

BEHAVIORAL

Nutrition Goals (Yes)

Participant will be assigned a personalized weekly nutrition goal related to nutrition monitoring condition.

BEHAVIORAL

Nutrition Goals (No)

Participant will not be assigned a personalized weekly nutrition goal.

BEHAVIORAL

Supportive Text Messages (Yes)

Participant will receive up to 5 supportive text-messages from the study staff per week.

BEHAVIORAL

Supportive Text Messages (No)

Participant will not receive supportive text-messages.

BEHAVIORAL

Lesson Delivery (Once)

All behavioral lessons will be made available to participant simultaneously.

BEHAVIORAL

Lesson Delivery (Weekly)

A new behavioral lesson will be made available to participant weekly throughout the 12 weeks.

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • UNC Lineberger Comprehensive Cancer Center

    lead OTHER

Principal Investigators

  • Erin M Coffman, MA · University of North Carolina, Chapel Hill

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-02
Primary Completion
2024-09-30
Completion
2024-09-30

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 NCT05887401 on ClinicalTrials.gov