Actively Recruiting
Aha BOOST Arm-hand BOOST Therapy to Enhance Recovery After Stroke: Clinical, Health Economic and Process Evaluation
Led by KU Leuven · Updated on 2026-03-19
80
Participants Needed
2
Research Sites
180 weeks
Total Duration
On this page
Sponsors
K
KU Leuven
Lead Sponsor
V
Vrije Universiteit Brussel
Collaborating Sponsor
AI-Summary
What this Trial Is About
The overall aim of this study is to establish the clinical- and cost-effectiveness of the arm-hand BOOST therapy when delivered on top of the usual care program in the sub-acute phase post stroke and to perform a process evaluation. In this phase III RCT, 80 patients with stroke will be recruited from two inpatient stroke rehabilitation wards in Belgium and randomized to the experimental group receiving arm-hand BOOST therapy or the control group receiving the L-BOOST intervention, on top of their usual inpatient care program. The arm-hand BOOST program (1 hour/day, 5x/week, 4 weeks) consists of group exercises based on four key aspects, namely neurophysiology, sequences of reaching and grasping, de-weighting of the arm, and orientation of the hand towards objects. Additionally, technology-supported upper limb therapy will be provided two times 30 minutes per week. The L-BOOST intervention comprises a dose-matched program of lower limb exercises and general reconditioning. At baseline, after 4 weeks of training, 3 months after the intervention and at 12 months post stroke, outcome assessment will be performed. The primary outcome measure is the action research arm test (ARAT). Secondary outcomes include measures in the domain of upper limb function and capacity, independence, participation and quality of life. Multivariate ANOVA and sensitivity analyses will be used to compare change from baseline between groups. Information on medical costs will be collected to allow a health economic evaluation. Finally, a process evaluation will be performed to assist in identifying why arm-hand BOOST succeeds or fails unexpectedly or has unanticipated consequences, and how this can be optimized. At the start of this study the investigators hypothesize that: (I) Aha BOOST will result in a significant greater improvement in arm-hand activity post-intervention, at follow-up and 12 months post stroke compared to control therapy (L-BOOST); (II) Aha BOOST will result in a significant greater improvement in upper limb function, performance, independence and activity of daily living, and participation post-intervention, at follow up and 12 months post stroke. (III) Investing in 24 hours of extra arm-hand therapy to subacute stroke patient in the inpatient rehabilitation setting can reduce the health-economic and societal cost 12 months post stroke.
CONDITIONS
Official Title
Aha BOOST Arm-hand BOOST Therapy to Enhance Recovery After Stroke: Clinical, Health Economic and Process Evaluation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Stroke occurred within the past 5 months
- Age 18 years or older
- Expected to remain inpatient for at least 4 weeks
- Able to sit independently
- Motor impairment in the upper limb, defined by specific scores on the Fugl-Meyer assessment upper extremity (FMA-UE)
You will not qualify if you...
- Severe communication difficulties, defined by a score below 24 on the visual sentence comprehension test
- Severe cognitive impairment, defined by a score below 18 on the Montreal Cognitive Assessment
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Revalidatieziekenhuis RevArte
Edegem, Antwerpen, Belgium, 2650
Actively Recruiting
2
Revalidatiecentrum K7 UZ Gent
Ghent, Oost-Vlaanderen, Belgium, 9000
Not Yet Recruiting
Research Team
G
Geert Verheyden, Professor
CONTACT
S
Sarah Meyer, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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