Actively Recruiting
Supporting Daily Functioning of Persons With a Neurological Disorder: (Cost)Effectiveness of Occupational Therapy at Home E-Rehabilitation (OTHER) for Persons Post-stroke
Led by Amsterdam University of Applied Sciences · Updated on 2025-09-10
171
Participants Needed
9
Research Sites
N/A
Total Duration
On this page
Sponsors
A
Amsterdam University of Applied Sciences
Lead Sponsor
Z
ZonMw: The Netherlands Organisation for Health Research and Development
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to evaluate the effectiveness and cost-effectiveness of an Occupational Therapy at Home E-Rehabilitation (OTHER) program compared to usual occupational therapy care for older adults recovering from stroke. The study focuses on community-dwelling older persons post-stroke who are undergoing geriatric rehabilitation. It seeks to understand how OTHER impacts self-perceived daily activity performance, satisfaction, physical activity, self-management, and quality of life over a 24-week period. The trial also explores participants' and therapists' experiences with the intervention and factors influencing its delivery. Participants are randomly assigned to either usual care, which involves standard geriatric rehabilitation after returning home, or the OTHER intervention. The OTHER program includes activity monitoring, coaching by an occupational therapist, and videoconferencing support, starting during inpatient rehabilitation and continuing for 12 weeks after discharge. This approach aims to optimize the transition from clinical care to home-based rehabilitation. Throughout the study, researchers will assess changes in daily activity performance using the Canadian Occupational Performance Measure at one, three, and six months. Additional evaluations include self-management, physical activity levels, mobility, quality of life, satisfaction with occupational therapy, and societal costs. Data collection includes baseline and follow-up assessments at 4, 12, and 24 weeks after discharge. The total participation duration is about 26 weeks, allowing for comprehensive monitoring and comparison of outcomes between groups.
CONDITIONS
Brief Title
Effect of Occupational Therapy at Home E-Rehabilitation (OTHER) for Persons Post-stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be able to walk a few steps with or without a walking device
- Be 60 years or older
- Have a Montreal Cognitive Assessment (MoCA) score of at least 16
- Have an indication for follow-up geriatric rehabilitation at home
You will not qualify if you...
- Are terminally ill
- Have severe aphasia or problems with understanding
- Have been legally assessed as incapable by a geriatric doctor
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 weeks after discharge
Participants receive occupational therapy at home using activity monitoring and coaching via videoconference for 12 weeks following discharge from inpatient geriatric rehabilitation or hospital.
Weekly visits via videoconference
Duration - Up to 24 weeks after discharge
Participants are assessed for changes in occupational performance, self-management, quality of life, mobility, and satisfaction with therapy up to 24 weeks after discharge.
4 visits at 4, 12, and 24 weeks after discharge
Trial Site Locations
Total: 9 locations
1
Behandelcentrum SZR
Tiel, Gelderland, Netherlands, 4003 CA
Actively Recruiting
2
ZZG Herstelcentrum
Groesbeek, Gerlderland, Netherlands, 6561 LE
Actively Recruiting
3
Cicero Zorggroep
Brunssum, Limburg, Netherlands, 6441 CR
Actively Recruiting
4
Sevagram
Heerlen, Limburg, Netherlands, 6419 PB
Actively Recruiting
5
TanteLouise
Bergen op Zoom, North Brabant, Netherlands, 4613 AK
Actively Recruiting
6
Hogeschool van Amsterdam
Amsterdam-Zuidoost, North Holland, Netherlands, 1105 BD
Actively Recruiting
7
GRZ Plus (2 locations, Omring and Zorgcirkel)
Hoorn, North Holland, Netherlands, 1624 AB
Actively Recruiting
8
Vivium Naardenheem
Naarden, North Holland, Netherlands, 1411 HB
Actively Recruiting
9
AxionContinu
Utrecht, Utrecht, Netherlands, 3526KJ
Actively Recruiting
Research Team
S
Sanne Pellegrom, MSc.
M
Margriet Pol, Dr
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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