Clinical Applicability of Robot-assisted Gait Training System in Acute Stroke Patients

Sponsor
China Medical University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02755415
Collaborator
(none)
60
1
2
19
3.2

Study Details

Study Description

Brief Summary

Investigation of the clinical feasibility and efficacy of a newly developed robot-assisted gait training system for acute stroke survivors. It is anticipated that robot-assisted gait rehabilitation will achieve significantly better gait and quality of life outcomes than the standing table rehabilitation.

Condition or Disease Intervention/Treatment Phase
  • Device: HIWIN Robotic Gait Training System
  • Other: Static Standing Table
N/A

Detailed Description

Stroke is not only the second leading cause of mortality in Taiwan, it is also the primary cause of long-term physical and psychological disabilities in our society. Array of reasons have been suggested to be an obstacle for stroke patients to receive adequate physical rehabilitation, including the lack of physical capacity, severe neurological deficits or the loss of strength. Given the critical importance of high-intensity and high-repetitiveness of early rehabilitation for stroke patients in achieving sustainable long term outcomes, robot-assisted gait rehabilitation devices have gained great interest in the last decade and is slowly becoming part of the clinical rehabilitation program for stroke patients. However, despite the growing interest and the significant resources invested for the development of robot-assisted rehabilitation devices, there still lacks empirical evidence of its clinical applicability for stroke patients. Moreover, available evidence to date have mostly focused on sub-acute and chronic stroke patients and investigation in acute stroke population, especially in those with complete incapacitation for ambulation, is sparse. It is therefore the aim of the proposed project to fulfil this significant gap in our clinical knowledge by comparatively investigate the clinical applicability of a recently developed HIWIN Robotic Gait Training System (MRG-P100) against the traditional rehabilitation program with an emphasis on the determination of psychological and functional capacity recovery status in acute stroke survivors.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Clinical Applicability of Robot-assisted Gait Training System in Acute Stroke Patients
Study Start Date :
May 1, 2016
Anticipated Primary Completion Date :
Apr 1, 2017
Anticipated Study Completion Date :
Dec 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Static Standing Table Training

Patients in this group will receive standard hospital based rehabilitation as well as static standing table training

Other: Static Standing Table
As part of the standard hospital rehabilitation, static standing table allows patient to be in a fully supported standing position

Experimental: Robotic Gait Training

Patients in this group will receive standard hospital based rehabilitation as well as robot-assisted gait rehabilitation training

Device: HIWIN Robotic Gait Training System
HIWIN Robotic Gait Training System is an automatic training system that combines weight-bearing standing, repetitive stepping and gait training

Outcome Measures

Primary Outcome Measures

  1. Berg Balance Scale [15-20 minutes]

    The Berg Balance Scale (or BBS) is a widely used clinical test of a person's static and dynamic balance abilities and is generally considered to be the gold standard for clinical practice

Secondary Outcome Measures

  1. Pittsburgh Sleep Quality Index [10-15 minutes]

    The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The questionnaire has been used in many settings, including research and clinical activities, and has been used in the diagnosis of sleep disorders

  2. EuroQol five dimensions questionnaire (EQ-5D) [10-15 minutes]

    EuroQol five dimensions questionnaire (EQ-5D) is a standardized instrument for measuring generic health status.

  3. Resting muscle tone [10 minutes]

    A device developed by Myoton Technology (Myoton AS, Estonia) will be used to determine the resting muscle tone (oscillation frequency [Hz]) of the tibialis anterior muscle, gastrocnemius muscle, rectus femoris muscle and biceps femoris muscle.

  4. Resting muscle elasticity [10 minutes]

    A device developed by Myoton Technology (Myoton AS, Estonia) will be used to determine the resting muscle elasticity (Oscillation stiffness [N/m]) of the tibialis anterior muscle, gastrocnemius muscle, rectus femoris muscle and biceps femoris muscle.

  5. Six minute walk test [6 minutes]

    The six-minute walk test (6MWT) measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface. The goal is for the individual to walk as far as possible in six minutes. The individual is allowed to self-pace and rest as needed as they traverse back and forth along a marked walkway.

  6. Beck's depression Inventory [7-10 minutes]

    The Beck Depression Inventory (BDI) is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Between the age of 20-80 years;

  • Diagnosis of first, single unilateral cortical-subcortical acute stroke verified by brain imaging;

  • Paresis of a lower limb;

  • Ability to walk for only a few meters either with or without aid.

Exclusion Criteria:
  • Deemed by a physician to be medically unstable;

  • Other prior musculoskeletal conditions that affected gait capacity;

  • Co-existence of other neurological diseases;

  • Cognitive impairments that would impact on the safe participation in the study (MMSE<23)

Contacts and Locations

Locations

Site City State Country Postal Code
1 China Medical University Hospital Taichung Taiwan 408

Sponsors and Collaborators

  • China Medical University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
China Medical University Hospital
ClinicalTrials.gov Identifier:
NCT02755415
Other Study ID Numbers:
  • CMUH105-REC1-037
First Posted:
Apr 28, 2016
Last Update Posted:
Jul 27, 2016
Last Verified:
Jul 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by China Medical University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 27, 2016