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MERLIN: hoMEcare aRm rehabiLItatioN

MERLIN: hoMEcare aRm rehabiLItatioN - MERLIN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON48182
Enrollment
15
Registered
2019-05-16
Start date
2019-08-14
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cerebrovasculair accident Stroke

Interventions

The intervention consists of training for six weeks with Merlin for minimal 3 hours per week divided over minimally 4 to maximal 7 sessions. The time between training session should be at least 24 h

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: unilateral paresis, first incidence of stroke, minimal 6 months, maximum 3 years post stroke, Fugl-Meyer Assessment-Upper extremity score below 50, able to perform 3 times finger extension and have some proximal voluntary movement capability, ability to give informed consent, visual and cognitive ability to participate in the protocol, understand dutch or english language, know how to operate a computer (of someone to help)

Exclusion criteria

Exclusion criteria: (Self-reported) depression, other rheumatologic, orthopaedic or neurological disorders, following occupational or physiotherapy specifically focussed on the arm/hand

Design outcomes

Primary

MeasureTime frame
The main study outcome is the Wolf Motor Function Test (WMFT). This wil be tested six weeks before the intervention (T0), just before the start of the intervention (T1) and after the six weeks of intervention (T2). To examine the retention, these tests will be performed again six weeks after the end of the intervention (T3) and after 6 months (T4).

Secondary

MeasureTime frame
Secondary outcomes are the Action Research Arm Test (ARAT), Fugl-Meyer Assessment-Upper Extermity (FMA-UE), Intrinsic Motivation Inventory (IMI), System Usability Scale (SUS), Dutch Quebec User Evaluation of Satisfaction with Assistive Technology (D-QUEST) and EuroQol-5D (EQ-5D) and biomechanical data using the ArmAssist Assessment (AAA). Subjective opinion will be assessed during in-depth interviews.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)