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The influence of a robot-mediated functional arm training protocol on arm function of chronic stroke patients

The influence of a robot-mediated functional arm training protocol on arm function of chronic stroke patients - Robotic functional arm training for chronic stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON31273
Enrollment
15
Registered
2007-05-01
Start date
2008-04-24
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

cerebrovascular accident stroke

Interventions

The intervention consists of a training program of 6 weeks of upper extremity training of reaching and grasping exercises, supplemented to (potential) regular stroke rehabilitation. Training session

Sponsors

Revalidatiecentrum Het Roessingh
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Stroke at least 6 months prior to admittance to experiment Right upper extremity affected (experimental set-up only suitable for right arm) Receiving/having received treatment at the Roessingh Centre of Rehabilitation Ability to lift arm (partly) against gravity

Exclusion criteria

Exclusion criteria: Shoulder pain, either in rest or in movement Additional neurologic, orthopaedic or rheumatologic disease of right upper extremity, which is likely to interfere with mobility and/or strenght of the arm Inability to understand and follow instructions

Design outcomes

Primary

MeasureTime frame
Primary study parameters are intra-subject changes in muscle activity and biomechanics of arm movements (at the impairment level).

Secondary

MeasureTime frame
The Fugl-Meyer assessment, the Motricity Index (both are clinical scores of the motor status of the arm) and the Action Research Arm Test (for functional abilities of the arm) are included to examine changes at the functional level.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)