Implementing affordable technology to improve mobility and physical activity in an inpatient rehabilitation setting; a feasibility study.
- Conditions
- Mobility limitationsPhysical inactivityPhysical Medicine / Rehabilitation - PhysiotherapyNeurological - Other neurological disorders
- Registration Number
- ACTRN12621000938808
- Lead Sponsor
- Prince of Wales Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Patients receiving the clinical intervention:
Adults admitted to the Prince of Wales Hospital for rehabilitation with
• reduced mobility (Short Physical Performance Battery score of less than 12/12)
• a clinician-assessed capacity for improvement in mobility
• a likely life expectancy of more than 6 months, estimated by a score of three or less on a modified version of the Implicit Illness Severity Scale
• an anticipated length of stay of at least 3 weeks from the date of randomisation
Therapists receiving the implementation strategies and delivering the clinical intervention:
Eligible therapists will be physiotherapists employed within SESLHD who provide inpatient rehabilitation to people with decreased mobility in the Rehabilitation ward (Parks 1 West) of Prince of Wales Hospital.
Exclusion criteria for patient-participants will be:
• a marked cognitive impairment (MMSE <24 or MoCA <18) unless caregiver present and willing and able to use digital devices with patient
• insufficient English language skills to participate in rehabilitation.
• inadequate vision to use the devices (less than 6/18 on the Snellen Chart)
• a medical condition precluding exercise (unstable cardiac disease, uncontrolled hypertension, uncontrolled metabolic diseases, large abdominal aortic aneurysm or a weight-bearing restriction)
• inability to balance safely in standing despite the assistance of a staff member or the nominated support person or walking aid
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method