- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01117194
Effect on Shoulder Training Using Rehabilitation Robot for Stroke Patients
December 20, 2012 updated by: National Taiwan University Hospital
Rehabilitation Robot for Upper Limbs, Component Project 5: Effect on Shoulder Training Using Rehabilitation Robot for Stroke Patients
The purpose is to study the effect of rehabilitation robot on shoulder training for stroke patients.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
12
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Taipei, Taiwan, 100
- Recruiting
- Dpt. Physical Medicine and Rehabilitation, NTUH
-
Contact:
- Wen-Shiang Chen
- Phone Number: 67087 +886-2-2123456
- Email: wenshiang@gmail.com
-
Principal Investigator:
- Wen-Shiang Chen, MD PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- stroke (1-3 months)
- Brunnstrom Stage II-III
- single, unilateral
Exclusion Criteria:
- aphasic
- shoulder impairment
- severe osteoporosis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: control group
|
|
|
Experimental: shoulder training, rehabilitation robot
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Use an intelligent robot to assist upper limb rehabilitation.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Barthel index,
Time Frame: 1 year
|
1 year
|
|
Modified Asworth Scale
Time Frame: 1 year
|
1 year
|
|
STREAM and PASS scales
Time Frame: 1 year
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
shoulder range of motion, VAS
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Wen-Shiang Chen, MD, PhD, Dpt. Physical Medicine and Rehabilitation, NTUH Taipei, Taiwan
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2010
Primary Completion (Anticipated)
February 1, 2013
Study Completion (Anticipated)
February 1, 2013
Study Registration Dates
First Submitted
January 18, 2010
First Submitted That Met QC Criteria
May 4, 2010
First Posted (Estimate)
May 5, 2010
Study Record Updates
Last Update Posted (Estimate)
December 21, 2012
Last Update Submitted That Met QC Criteria
December 20, 2012
Last Verified
November 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 200804031D
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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