Effects of wrist limited dynamic splint on carpal tunnel syndrome
Not Applicable
- Conditions
- Carpal tunnel syndrome.Carpal tunnel syndrome
- Registration Number
- IRCT2015061522753N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 24
Inclusion Criteria
the subjects gender should be female; the patients diagnosis should be carpal tunnel syndrome by a physiatrist doctor; the severity of illness should be mild or moderate; the subjects should be able to understand and do the orders of the tests.
Exclusion criteria: history of surgery on the affected hand; systemic illnesses; pregnancy; subjects who do not cooperate; subjects who do not have the results of neural conductive tests.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Function. Timepoint: Before and after the 6 weeks treatment. Method of measurement: Boston carpal tunnel syndrome questionnaire.;Symptome severity. Timepoint: Before and after the 6 weeks treatment. Method of measurement: Boston carpal tunnel syndrome questionnaire.;Grip strength. Timepoint: Before and after the 6 weeks treatment. Method of measurement: MIE digital device.;Pinch strength. Timepoint: Before and after the 6 weeks treatment. Method of measurement: MIE digital device.;Dexterity. Timepoint: Before and after the 6 weeks treatment. Method of measurement: Purduepeg board test.;Median nerve sensory conductive velocity. Timepoint: Before and after the 6 weeks treatment. Method of measurement: MEDLEC SYNERGY VIASIS electromiography device.;Median nerve distal sensory latency. Timepoint: Before and after the 6 weeks treatment. Method of measurement: MEDLEC SYNERGY VIASIS electromiography device.
- Secondary Outcome Measures
Name Time Method