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Arm support treatment in the early phase after stroke.

Arm support treatment in the early phase after stroke.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26063
Enrollment
70
Registered
2010-09-29
Start date
2010-12-01
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

stroke, cerebrovascular accident beroerte, cerebrovasculair accident

Interventions

The participants receive reach training for the affected arm during 6 weeks, 3 times 30 minutes per week. The intervention group (35 persons) will train using the ArmeoBoom system for arm support and

Sponsors

Roessingh Research and Development
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Start of participation between 1 and 12 weeks post first-ever stroke; 2. Hemiparetic arm, with ability of some elbow extension (MRC score 2 or 3 out of 5); 3. Ability to understand and follow instructions; 4. Ability to endure training and evaluation sessions.

Exclusion criteria

Exclusion criteria: Co-morbidity of other diseases (incl. pain) that limit use of the arm.

Design outcomes

Primary

MeasureTime frame
Before and after training changes in overall arm function (Fugl-Meyer assessment, Stroke Upper Limb Capacity Scale) and work area are quantified.

Secondary

MeasureTime frame
User experience of therapist and patient (semi-structured interviews) are identified after training. Both before and after training a Visual Analog Scale for pain is filled in by patients.

Contacts

Public ContactA.I.R. Kottink-Hutten

Roessingh Research and Development, Roessinghsbleekweg 33b

a.kottink@rrd.nl+31 (0)53 4875733

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)