Actively Recruiting
Tele-reha Versus Paper-based Aftercare Programme Following Inpatient Rehabilitation
Led by Medical University of Vienna · Updated on 2024-12-09
285
Participants Needed
1
Research Sites
78 weeks
Total Duration
On this page
Sponsors
M
Medical University of Vienna
Lead Sponsor
N
Neurologisches Rehabiliationszentrum Rosenhügel
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this three-armed, observer-blinded, randomised controlled trial is to (i) to implement a telerehabilitation intervention in routine care after an inpatient rehabilitation stay for people insured with the Social Insurance Institution for the Self-Employed (SVS), (ii) to evaluate the impact of telerehabilitation on the consolidation of goals achieved during the inpatient stay in everyday life, and (iii) to evaluate whether independence in everyday life can be increased by implementing telerehabilitation at home compared to standard care. Our hypothesis is that the tele-reha intervention, including ongoing therapist support, will improve independence in daily living (defined as the primary outcome of this study), as measured by the Functional Assessment Measure (FAM), compared to a control group receiving a standard paper-based program.
CONDITIONS
Official Title
Tele-reha Versus Paper-based Aftercare Programme Following Inpatient Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years or older
- Experiencing problems with motor function, sensory function, cognition, swallowing, or speech production
- Insured with the Social Insurance Institution for the Self-Employed (SVS)
- Agreeing to telerehabilitation after discharge
- Having sufficient motor and cognitive abilities to operate a smartphone, tablet, or PC or supported by caregivers
- Able to independently perform the assigned therapy tasks
You will not qualify if you...
- Severe impairments in awareness, memory, attention, spatial performance, executive function, apraxia, speech, or visual perception that prevent safe study participation as judged by treating physicians or therapists
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Medical University of Vienna
Vienna, State of Vienna, Austria, 1090
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here