Shoulder pain is related to somatosensory and nociceptive changes in the acute phase after stroke. These changes may indicate the involvement of specific mechanisms (nociceptive, neuropathic) of post-stroke shoulder pain. Changes may either precede…
ID
Bron
Verkorte titel
Aandoening
stroke, post-stroke shoulder pain
CVA, hemiplegische schouderpijn
Ondersteuning
Roessingh Rehabilitation Center
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Baseline assessment consists of a questionnaire that assesses pain complaints (current, past), clinical neurological tests (touch, temperature, sharpness) and tests for motor function. Moreover, general neurologic status and emotional status are assessed. Follow-up measurements consist of the assessment of pain complaints (quality, quantity) and the assessment of somatosensory and nociceptive changes using quantitative sensory testing and cold pressor testing.
Achtergrond van het onderzoek
Shoulder pain is a common complication after stroke and in some cases difficult to treat. Better prevention in the acute stroke phase and appropriate treatment in of shoulder pain may be accomplished when more is known about the neurophysiological mechanisms underlying the development and chronification of shoulder pain after stroke. The objective of the study is to identify somatosensory and nociceptive changes in the acute phase after stroke in relation to the development of shoulder pain.
Doel van het onderzoek
Shoulder pain is related to somatosensory and nociceptive changes in the acute phase after stroke. These changes may indicate the involvement of specific mechanisms (nociceptive, neuropathic) of post-stroke shoulder pain. Changes may either precede or follow the development of shoulder pain.
Onderzoeksopzet
1. Baseline: 0-2 weeks post-stroke;
2. Follow up 1: 3 months post-stroke;
3. Follow up 2: 6 months post-stroke.
Onderzoeksproduct en/of interventie
N/A
Publiek
M. Roosink
University of Twente, Biomedical Signals and Systems
Enschede 7500 AE
The Netherlands
+31 (0)53 4892740
m.roosink@utwente.nl
Wetenschappelijk
M. Roosink
University of Twente, Biomedical Signals and Systems
Enschede 7500 AE
The Netherlands
+31 (0)53 4892740
m.roosink@utwente.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Older than 18 years;
2. Legally competent;
3. Able to communicate;
4. First-ever unilateral CVA (ischemic or hemorrhagic) of the middle cerebral artery (if possible confirmation by CT or MRI scan);
5. Somatosensory and motor loss during baseline measurement (0-2 weeks after stroke);
6. Sign informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Pregnancy;
2. HIV/AIDS;
3. Any other brain disease (trauma, tumor, parkinson, multiple sclerosis);
4. Any peripheral neurological disease (amputation, neuropathy);
5. Pre-existent psychiatric disorders;
6. Pre-existent use of psychotropic substances or medication;
7. Chronic pain complaint (> 3 subsequent months) in the 6 months prior to stroke.
Opzet
Deelname
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| Register | ID |
|---|---|
| NTR-new | NL1648 |
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