Trial record 18 of 198 for:    stroke [CONDITION] AND rehabilitation [TREATMENT] | Open Studies

Effect on Shoulder Training Using Rehabilitation Robot for Stroke Patients

This study is currently recruiting participants. (see Contacts and Locations)
Verified November 2012 by National Taiwan University Hospital
Sponsor:
Information provided by (Responsible Party):
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT01117194
First received: January 18, 2010
Last updated: December 20, 2012
Last verified: November 2012
  Purpose

The purpose is to study the effect of rehabilitation robot on shoulder training for stroke patients.


Condition Intervention Phase
Stroke
Device: Rehabilitation Robot for Upper Limb Dysfunction (NTUH Model One)
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Prevention
Official Title: Rehabilitation Robot for Upper Limbs, Component Project 5: Effect on Shoulder Training Using Rehabilitation Robot for Stroke Patients

Resource links provided by NLM:


Further study details as provided by National Taiwan University Hospital:

Primary Outcome Measures:
  • Barthel index, [ Time Frame: 1 year ] [ Designated as safety issue: No ]
  • Modified Asworth Scale [ Time Frame: 1 year ] [ Designated as safety issue: No ]
  • STREAM and PASS scales [ Time Frame: 1 year ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • shoulder range of motion, VAS [ Time Frame: 1 year ] [ Designated as safety issue: No ]

Estimated Enrollment: 12
Study Start Date: January 2010
Estimated Study Completion Date: February 2013
Estimated Primary Completion Date: February 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: shoulder training, rehabilitation robot Device: Rehabilitation Robot for Upper Limb Dysfunction (NTUH Model One)
Use an intelligent robot to assist upper limb rehabilitation.
Other Name: self-developed robotic arm
No Intervention: control group

  Eligibility

Ages Eligible for Study:   50 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • stroke (1-3 months)
  • Brunnstrom Stage II-III
  • single, unilateral

Exclusion Criteria:

  • aphasic
  • shoulder impairment
  • severe osteoporosis
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01117194

Contacts
Contact: Wen-Shiang Chen +886-2-2123456 ext 67087 wenshiang@gmail.com

Locations
Taiwan
Dpt. Physical Medicine and Rehabilitation, NTUH Recruiting
Taipei, Taiwan, 100
Contact: Wen-Shiang Chen    +886-2-2123456 ext 67087    wenshiang@gmail.com   
Principal Investigator: Wen-Shiang Chen, MD PhD         
Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Principal Investigator: Wen-Shiang Chen, MD, PhD Dpt. Physical Medicine and Rehabilitation, NTUH Taipei, Taiwan
  More Information

No publications provided

Responsible Party: National Taiwan University Hospital
ClinicalTrials.gov Identifier: NCT01117194     History of Changes
Other Study ID Numbers: 200804031D
Study First Received: January 18, 2010
Last Updated: December 20, 2012
Health Authority: Taiwan: Department of Health

Additional relevant MeSH terms:
Stroke
Cerebral Infarction
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases
Brain Infarction
Brain Ischemia

ClinicalTrials.gov processed this record on July 22, 2014