A Preliminary Feasibility Efficacy of Participation in Daily Life Promotion Program

NCT ID: NCT02802956

Last Updated: 2016-06-16

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-06-30

Study Completion Date

2018-12-31

Brief Summary

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Efficacy of Participation in Daily Life Promotion Program for Patients with Chronic Stroke

Detailed Description

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The purpose of this three-year research project is to develop an intervention program to promote participation in daily life for patients with chronic stroke and to evaluate its efficacy.

Conditions

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Stroke

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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intervention group

Daily Life Promotion Program

Group Type EXPERIMENTAL

Daily Life Promotion Program

Intervention Type OTHER

Daily Life Promotion Program

control group

general rehabilitation treatment

Group Type EXPERIMENTAL

general rehabilitation treatment

Intervention Type OTHER

general rehabilitation treatment

Interventions

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Daily Life Promotion Program

Daily Life Promotion Program

Intervention Type OTHER

general rehabilitation treatment

general rehabilitation treatment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient with stroke after 6 months.
* Must be able to follow orders and no other cognition impairment, Mini Mental State Examination scale must \>20.

Exclusion Criteria

* Clinical diagnosis of Dementia or Psychosis.
* Clinical diagnosis of Musculoskeletal disorders or Nervous system diseases.
* Patient with Congestive Heart Failure, Hypertension, Atrial fibrillation.
* Could not communication with others.
* Foreigner.
Minimum Eligible Age

20 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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Taiwan

Central Contacts

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I MING HSIAO

Role: CONTACT

886-2-23123456*70420

Yi-Jiun Yang

Role: CONTACT

886-2-23123456*66763

Facility Contacts

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Yang Yi-Jiun, BS

Role: primary

886-2-23123456 ext. 67313

Other Identifiers

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201509087RINC

Identifier Type: -

Identifier Source: org_study_id

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