N/A
N=5
Sustaining Physical Activity Following Cardiac Rehabilitation Completion
Cardiac Rehabilitation
Bottom Line
View on ClinicalTrials.gov: NCT03991715 ↗Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Jul 2019
Primary outcome: Primary: Average Steps Per Day (Preintervention Period) — 6507 steps per day
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Activity Tracker (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of North Carolina, Chapel Hill
- Primary completion
- Mar 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Average Steps Per Day (Preintervention Period) |
6507 | — |
| PRIMARY Average Physical Activity in Minutes Per Day (Preintervention Period) |
14 | — |
| PRIMARY Average Steps Per Day (Intervention Period) |
5960 | — |
| PRIMARY Average Physical Activity in Minutes Per Day (Intervention Period) |
11 | — |
| PRIMARY Average Steps Per Day (Maintenance Period) |
5158 | — |
| PRIMARY Average Physical Activity Per Day (Maintenance Period) |
7 | — |
Summary
Cardiac rehabilitation participants will be enrolled during cardiac rehabilitation and provided an activity tracker to use.
Eligibility Criteria
Inclusion criteria
- coronary heart disease
- currently attending cardiac rehabilitation with at least 4 weeks left
- >=18 years of age
- own a smart phone and able to participate in mobile health program
- able to understand and write English
- adequate clinical stability
- understand and sign informed consent
Exclusion criteria
- currently using a digital physical activity tracker
- past use of a digital activity tracker
- planning to relocate in 12 weeks
- acute coronary artery disease symptoms
- decompensated heart failure
- New York Heart Association class IV heart failure
- severe valvular heart disease
- severe pulmonary hypertension
- cardiac transplantation
- visually impaired, severe
- end stage renal disease
- impairment from stroke, injury, or other medical disorder that precludes participation
- dementia that precludes ability to participate and follow protocol
- inability or unwillingness to comply with study requirements
Data sourced from ClinicalTrials.gov (NCT03991715). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.