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Care prevention support system using health-care robot A randomized controlled trial based on Kanagawa Me-Byo Prospective study

Not Applicable
Conditions
Frailty
Registration Number
JPRN-UMIN000042352
Lead Sponsor
Kanagawa University of Human Service
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

Persons who cannot obtain informed consent from the person regarding the contents of the consent confirmation document Person who has difficulty filling out questionnaire Those who have difficulty communicating in Japanese Those who judge that it is inappropriate to implement an intervention program in view of physical and psychological burdens Persons who have difficulty wearing HAL due to body size disagreement such as weight, thigh length, lower leg length, waist width, or due to large deformation of the body Persons who are judged by a doctor to be inappropriate for wearing or using HAL, such as improper standing / walking exercises Persons who cannot attach electrodes due to skin diseases or allergies Persons who cannot take measures to prevent falls

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Walking speed
Secondary Outcome Measures
NameTimeMethod
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