The use of the Dutch version of the Movement Specific Reinvestment Scale (MSRS) in rehabilitatio
Completed
- Conditions
- CVAStroke10007963
- Registration Number
- NL-OMON33813
- Lead Sponsor
- Hoensbroek Revalidatiecentrum (HRC)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 130
Inclusion Criteria
Participants have to meet following selection criteria:
a) clinically diagnosed stroke,
b) Age > 18 years
c) Sufficient cognitive level and communication skills to fill in the questionnaires (support in writing or reading is allowed) ;Addition for amendment :
Only patients who are able to walk independently (Functional Ambulation Category >= 3) will be asked to participate in the additional test.
Exclusion Criteria
Sever additional impairments prior to stroke
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Measuring points in part 1 are at entry in the study and three weeks later. In<br /><br>Part 2 measuring points are at entry (baseline- T0) and after 3, 6 and 9 weeks.<br /><br>In both parts of the study the following characteristics will be collected:<br /><br>age, gender, brain lesion site, co-morbidities or complications. The primary<br /><br>outcome is the *Movement Specific Reinvestment Scale*.<br /><br><br /><br>Additional test (amendment): Degree of which a participants performs worse<br /><br>during the stressfull situation (compared to the trainings situation). This<br /><br>will be operationalised by: numbers of falls/stumblings, number of times<br /><br>touching an obstacle,<br /><br>times of freezing (the times that the patient stops walking will be counted).</p><br>
- Secondary Outcome Measures
Name Time Method <p>As additional measurements on functional outcome are used: the Rivermead<br /><br>Mobility Index (part 1 and 2) and the Barthel Index (part2). To control for<br /><br>confounding, in part 2 the Cognitive Log and the Hospital Anxiety and<br /><br>Depression Scale are used.<br /><br><br /><br>Addiotional test (amendment):<br /><br>Both the patients and independent rater will be asked to judge the quality of<br /><br>the walking on a 10 point Likert scale. </p><br>