Actively Recruiting
Using a mHealth Intervention to Promote Physical Activity in Phase III Cardiac Rehabilitation Clients
Led by AdventHealth University · Updated on 2024-07-12
46
Participants Needed
1
Research Sites
147 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Using a mHealth Intervention to Promote Physical Activity in Phase III Cardiac Rehabilitation Clients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Currently receiving Phase III cardiac rehabilitation at Hope Clinic
- Age 18 years or older
- Able to read and communicate in English
- Able to follow instructions to walk
- Provided signed informed consent
- Willing to wear a Fitbit device throughout the study
- Own a smartphone with text messaging capability without undue financial burden
- Willing to receive text messages and phone calls from the research team
You will not qualify if you...
- Pregnant or lactating
- Scheduled for surgery or traveling within the next 8 weeks
- Currently participating in another health promotion program
- Physically sufficiently or overly active (averaging 7,500 or more steps per day based on a 1-week activity monitor)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
AdventHealth University
Orlando, Florida, United States, 32803
Actively Recruiting
Research Team
C
Chia-Wei Fan, MD
CONTACT
L
Leana Goncalves Araujo, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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