Home Telerehabilitation for Deconditioned Older Adults
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About
The purpose of this study is to develop a home exercise program for patients 60 years of age and over who are deconditioned following their discharge from the hospital, or recruited from GLA outpatient clinics. The program will be designed to monitor and improve patients' exercise behavior through the use of home technology, such as text messaging monitors.
Full description
The aim of this study is to develop and determine the feasibility of implementing a home exercise and functional status monitoring telerehabilitation program, known as TEL-REHAB, for older adults 60 years of age and over who are deconditioned following their discharge from the inpatient setting, or recruited from GLA outpatient clinics. Deconditioning is a modifiable risk factor for preventing institutionalization of frail elderly patients who would otherwise be able to live independently. Home exercise programs are an effective intervention to reduce the risk, but patient compliance with home exercise programs, and assessments of patients during home exercise programs, are barriers to achieving maximal benefits. Face-to-face visits with physical medicine professionals are an effective means to perform these functions, but are problematic because of professional time impacts and patient transportation problems. A TEL-REHAB program will empower these patients to take responsibility for their own health by providing ongoing communication with a healthcare provider. In this way, telerehabilitation may assist older adults to remain independent in their homes as long as possible.
Enrollment
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Volunteers
Inclusion criteria
- acute decline in functional status while hospitalized as reported by the patient
- physically inactive outpatients (exercise less than 30 min/day, 3 d/wk)
- ability to hear and communicate via telephone
- ability to read a video or text monitor
- ability to manually operate the technology
- have a working telephone and power source
- willingness to use the TEL-REHAB technology
Exclusion criteria
- does not speak English
- poor cognition as determined by the Mini-Cog
- non-ambulatory
- had a stroke, myocardial infarction, hip fracture, or total hip or knee replacement within the prior 6 months
Trial design
38 participants in 4 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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