RECRUITING

Using a mHealth Intervention to Promote Physical Activity in Phase III Cardiac Rehabilitation Clients

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

In this study, the investigators will implement a pilot project of using activity tracker (i.e., Fitbit) with phase III CR clients. The study will record the participants' daily steps and sleep patterns for 8 consecutive weeks in natural settings. Two specific aims are identified for this project: 1. Develop an intervention protocol using mHealth to promote Phase III CR clients' self-monitoring of PA. 2. Examine the efficacy of the intervention on clients' PA, sleep patterns, functional capacity and QoL.

Official Title

Using a mHealth Intervention to Promote Physical Activity in Phase III Cardiac Rehabilitation Clients

Quick Facts

Study Start:2023-02-17
Study Completion:2025-12-17
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05795036

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:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * currently receiving Phase III CR at Hope Clinic
  2. * are 18 years of age or older
  3. * can read and communicate in English
  4. * able to follow instructions to walk
  5. * provided signed informed consent
  6. * willing to wear Fitbit throughout the study
  7. * owns a smartphone with text messaging capability (participants need to decide ahead of time if they have a phone plan that is compatible with taking additional text messages without undue financial burden for themselves)
  8. * willing to receive text messages and phone calls from the research team.
  1. * are pregnant or lactating
  2. * have scheduled surgery or traveling within the next 8 weeks
  3. * currently participating in other health promotion program
  4. * sufficiently or overly active, as determined by a physical activity monitor worn for one week, indicating averaging ≥ 7,500 steps per day ("somewhat overly active").

Contacts and Locations

Study Contact

Chia-Wei Fan, MD
CONTACT
407-609-1388
chia-wei.fan@ahu.edu
Leana Goncalves Araujo, PhD
CONTACT
407-609-1388
leana.goncalvesaraujo@ahu.edu

Study Locations (Sites)

AdventHealth University
Orlando, Florida, 32803
United States

Collaborators and Investigators

Sponsor: AdventHealth University

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 Date2023-02-17
Study Completion Date2025-12-17

Study Record Updates

Study Start Date2023-02-17
Study Completion Date2025-12-17

Terms related to this study

Additional Relevant MeSH Terms

  • Cardiac Rehabilitation
  • Physical Activity