Using a mHealth Intervention to Promote Physical Activity in Phase III Cardiac Rehabilitation Clients
AdventHealth University
46 participants
Feb 17, 2023
INTERVENTIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria8
- currently receiving Phase III CR at Hope Clinic
- are 18 years of age or older
- can read and communicate in English
- able to follow instructions to walk
- provided signed informed consent
- willing to wear Fitbit throughout the study
- 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)
- willing to receive text messages and phone calls from the research team.
Exclusion Criteria4
- are pregnant or lactating
- have scheduled surgery or traveling within the next 8 weeks
- currently participating in other health promotion program
- 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").
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Interventions
Participants will use Fitbit device to self-monitor their physical activity in 8 weeks.
Participants will use Fitbit device to self-monitor their physical activity in 8 weeks. In addition, they will receive daily motivational text message.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05795036