A Preliminary Feasibility Efficacy of Participation in Daily Life Promotion Program
NCT ID: NCT02802956
Last Updated: 2016-06-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
30 participants
INTERVENTIONAL
2016-06-30
2018-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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intervention group
Daily Life Promotion Program
Daily Life Promotion Program
Daily Life Promotion Program
control group
general rehabilitation treatment
general rehabilitation treatment
general rehabilitation treatment
Interventions
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Daily Life Promotion Program
Daily Life Promotion Program
general rehabilitation treatment
general rehabilitation treatment
Eligibility Criteria
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Inclusion Criteria
* Must be able to follow orders and no other cognition impairment, Mini Mental State Examination scale must \>20.
Exclusion Criteria
* Clinical diagnosis of Musculoskeletal disorders or Nervous system diseases.
* Patient with Congestive Heart Failure, Hypertension, Atrial fibrillation.
* Could not communication with others.
* Foreigner.
20 Years
90 Years
ALL
No
Sponsors
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National Taiwan University Hospital
OTHER
Responsible Party
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Principal Investigators
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I MING HSIAO
Role: PRINCIPAL_INVESTIGATOR
National Taiwan University Hospital
Locations
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National Taiwan University Hospital
Taipei, Test2, Taiwan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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201509087RINC
Identifier Type: -
Identifier Source: org_study_id
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