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Mental practice based rehabilitation training aimed at improving arm function and performance of daily activities in stroke: a randomised clinical trial

Conditions
stroke
10007963
Registration Number
NL-OMON32124
Lead Sponsor
Hoensbroek Revalidatiecentrum (HRC)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
160
Inclusion Criteria

1. first ever stroke
2. post-stroke time of 2 - 6 weeks
3. clinically diagnosed central paresis of the arm/hand with strength MRC grade 1 to
3 of the elbow flexors at entry into the study
4. age between 18 and 85

Exclusion Criteria

1. severely impaired cognition
2. severe additional neurological, orthopaedic, rheumatoid impairments prior to
stroke
3. severely impaired communication as to comprehension

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Primary outcome measures for the effect evaluation are upper extremity<br /><br>functioning on the activity level scored based on:<br /><br>the Wolf motor Function test (WMFT); Frenchay Arm test (FAT) and based on<br /><br>accelerometry(ACC).</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary outcome measures are focussed on both the impairment:<br /><br>arm section of the Fugl Mayer test (FM)<br /><br>and the particpation level of the ICF:<br /><br>Impact on participation and Autonomy questionnaire (IPA), the stroke specific<br /><br>quality of life (SS-Qol) and the EuroQol 6D (EQ-6D). </p><br>
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