Preventieve armpositionering en elektrostimulatie bij CVA-patiënten.
Completed
- Conditions
- Stroke (CVA)
- Registration Number
- NL-OMON20103
- Lead Sponsor
- Prof. Klaas Postema, MD PhDUniversity Medical Center GroningenDepartment of Rehabilitation MedicinePostbus 300019700 RB GroningenTelephone: 050-3612295E-mail: k.postema@rev.umcg.nl
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 38
Inclusion Criteria
1. A first ever or recurrent stroke except subarachnoid hemorrhages;
2. Age above 18;
Exclusion Criteria
1. Any of the following contra indications for electrical stimulation:
A. Metal implants in the involved arm or shoulder;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Passive range of motion (PROM) of seven different arm movements will be assessed using a using a masked hydrogoniometer;<br /><br><br>2. Shoulder pain will be assessed using the ShoulderQ.
- Secondary Outcome Measures
Name Time Method 1. The degree of difficulty the patient and his/her primary carer have with activities related to the hemiplegic (spastic) arm is assessed with the Leeds Arm Spasticity Impact Scale (LASIS);<br /><br><br>2. Arm spasticity will be assessed using the Modified Tardieu Scale (MTS);<br /><br><br>3. The 66-point arm section of the Fugl-Meyer Assessment (FMA) will be used to assess the ability to make selective movements of the hemiplegic arm;<br /> <br><br>4. The degree of shoulder inferior subluxation is clinically graded in (half) fingerbreadths palpable below the acromion process in both shoulders.