Development of care techniques to reduce (alleviate) symptoms of pain and numbness as an aftereffect of stroke
Not Applicable
Recruiting
- Conditions
- stroke
- Registration Number
- JPRN-UMIN000052975
- Lead Sponsor
- Senri Kinran University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients who are judged by the attending physician, charge nurse, or principal investigator to be unsuitable as research participants at the time consent is obtained. 2.Patients who are judged by the attending physician, charge nurse, or principal investigator to be "unable to give effective informed consent due to language impairment, cognitive impairment, etc.". 3.Other patients who are judged by the principal investigator to be inappropriate as research participants.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Pain level: VAS (Visual Analogue Scale) [before and after the intervention, and upon waking and sleeping], SF-MPQ-2 (Short-Form McGill Pain Questionnaire-2) [before intervention, 1 month after, 2 months after]. 2. Presence and amount of analgesic medication [daily]. Impact on life: SF-12 (MOS 12-Item Short-Form Health Survey) [before, one month after, and two months after the intervention], HADS (Hospital Anxiety and Depression Scale) [before, one month after, and two months after the intervention], SIAS (Stroke Impairment Assessment Set) [before intervention]. 4. Relaxation effect: Heart rate variability [each time during intervention].
- Secondary Outcome Measures
Name Time Method