Pilot study for a randomized controlled trial on the actual condition of walking and improvement through instructio
Not Applicable
- Conditions
- one
- Registration Number
- JPRN-UMIN000050621
- Lead Sponsor
- Showa Pharmaceutical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
People with hypersensitivity to the materials in the Walking Impact Analysis System (Safety Walk Navi) and the rise test box. People with pain, swelling, inflammation, injury, or paralysis of the lower limbs and with limited ambulation. People who cannot be fitted with the Safety Walk Navi device. Persons who are otherwise deemed unsuitable as subjects by the principal investigator.(Keep a record of the reasons for exclusion.)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method