Wearable Technology to Reduce Sedentary Behavior and CVD Risk in Older Adults
Completed · Not applicable
Conditions studied: Cardiovascular Diseases
In brief
This study will evaluate the feasibility and efficacy of combining a traditional, structured exercise intervention with an innovative intervention designed to decrease sedentary behavior and increase non-exercise physical activity (NEPA).
Key facts
- Study ID
- NCT02632487
- Run by
- University of Florida
- People needed
- 58
- Starts
- 2016-04-01
- Expected to finish
- 2018-11-20
- Last updated by the study team
- 2018-11-23
Who can join
Age: 60 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Sedentary lifestyle, defined as <150 min/wk of moderate physical activity by CHAMPS questionnaire
- Moderate to high-risk of CHD events according to ATP-III risk classification algorithm
- Willingness to be randomized to either intervention group
- Willingness to participate in all study procedures
You may not qualify if…
- Failure to provide informed consent;
- Regular participation in an exercise training program within the last 3 months
- Absolute contraindication(s) to exercise training (American College of Sports Medicine guidelines)
- Office SBP > 180 mm Hg or DBP > 110 mm Hg
- Severe cardiac disease, i.e. NYHA Class III or IV congestive heart failure, clinically significant aortic stenosis, history of cardiac arrest, use of a cardiac defibrillator, or uncontrolled angina;
- Myocardial infarction or stroke within past year
- Significant cognitive impairment, i.e. known dementia or a Mini-Mental State Examination score < 24
- Progressive, degenerative neurologic disease, e.g., Parkinson's Disease, multiple sclerosis, ALS;
- Severe rheumatologic/orthopedic disease, e.g., awaiting joint replacement, active inflammatory disease
- Severe pulmonary disease, requiring either steroid pills or injections or the use of supplemental oxygen;
- Hip fracture, hip or knee replacement, or spinal surgery within past 4 months;
- Other significant co-morbid conditions that would impair ability to participate in the intervention
- Simultaneous participation in another intervention trial
Where it is running
- UF Clinical Translational Research Building — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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