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Robotic-assisted Locomotor Training on Mobility and Cardiopulmonary Function in Patients Suffering From Spinal Cord Injury

Primary Purpose

Spinal Cord Injury

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Robotic-assisted body weight supported treadmill training (Lokomat V6, Hocoma AG, Switzerland)
Passive lower limbs mobilization training (Motomed Vivo 2, RECK, Germany)
Sponsored by
Kowloon Hospital, Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injury focused on measuring Spinal cord injury, robotic, locomotion

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • adult patient with age 18 or above
  • suffering from incomplete spinal cord injury with classification B, C or D under the International Standards for Neurological Classification of Spinal Cord Injury (ISNSCI)
  • lesion level above or at T12; acquired the injury not more than 24 months at the time of recruitment
  • traumatic or non-traumatic, non-progressive lesion
  • able to tolerate standing on tilt-table in 90 degrees for more than 30 minutes
  • able to walk with or without orthosis but requires manual assistance in walking.

Exclusion Criteria:

  • fracture of spine or lower limbs which is not yet stabilized
  • severe osteoporosis or at high risk of pathological fracture
  • symptomatic postural hypotension; cardiac disease which is not recommended for moderate intensity exercise
  • severe muscle spasticity over lower limbs
  • severe lower limbs fixed contractures
  • leg length discrepancy for more than 2 centimeters
  • body weight exceeding 135 kilograms

Sites / Locations

  • Physiotherapy Department, Kowloon Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Robotic-assisted body weight supported treadmill training

Passive lower limbs mobilization training

Arm Description

Robotic assisted body weight supported treadmill training with conventional PT training

Passive lower limbs mobilization training with conventional PT training

Outcomes

Primary Outcome Measures

Change in Walking Index for Spinal Cord Injury version II from baseline to 8 weeks
A validated mobility independence assessment tool for spinal cord injury (SCI) population (Burns, Delparte, Patrick, Marino, & Ditunno, 2011). Subjects will be asked to walk on a 10-meter straight line and score will be given based on the use of walking aids, orthoses, manual assistance and distance covered.

Secondary Outcome Measures

Full Information

First Posted
November 8, 2013
Last Updated
January 25, 2019
Sponsor
Kowloon Hospital, Hong Kong
Collaborators
The Hong Kong Polytechnic University
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1. Study Identification

Unique Protocol Identification Number
NCT01989806
Brief Title
Robotic-assisted Locomotor Training on Mobility and Cardiopulmonary Function in Patients Suffering From Spinal Cord Injury
Official Title
Investigation on the Effect of Robotic-assisted Body Weight Supported Treadmill Training on Walking and Cardiopulmonary Recovery in Patients Suffering From Incomplete Spinal Cord Injury
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kowloon Hospital, Hong Kong
Collaborators
The Hong Kong Polytechnic University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Evidences showed that patients suffering from spinal cord injury (SCI) have poor mobility and higher chance to develop cardiopulmonary diseases, which leads to poor quality of life and shorter life expectancy. Different modalities were developed aiming at mobility restoration in SCI patients and robotic assisted body weight supported treadmill training is one of the latest technique in recent years. Yet there are scarce studies to investigate its effectiveness. The purpose of this study is to investigate the effectiveness of robotic-assisted body weight supported treadmill training on mobility and cardiopulmonary function of patients suffering from SCI by a randomized controlled trial. 80 patients suffering from incomplete SCI will be recruited for an 8-week training program. They will be randomized into either robotic assisted body weight supported treadmill training group or passive lower limb mobilization training group. The training effects will be measured by Walking Index for Spinal Cord Injury version II, lower extremity motor score, lower limb Modified Ashworth Scale, robotic gait system, gait analysis and gas analysis under sub maximal exercise stress test. Through the study, we intent to find the effectiveness of robotic-assisted body weight support treadmill training on walking and cardiopulmonary recovery with patients suffering from incomplete spinal cord injury. The hypothesis of the study is: Compared to the control group, robotic-assisted body weight supported treadmill training leads to a greater improvement in walking ability and cardiopulmonary functioning.
Detailed Description
Participants will be recruited from the spinal cord rehabilitation unit of Physiotherapy Department of Kowloon Hospital. Subjects will be allocated into intervention group or control group by using sealed envelope and they will be blinded for their group allocation. All participants will undergo standard physiotherapy program, including mobilization and strengthening exercise of limbs, trunk stabilization training, wheelchair maneuver training and overground walking training. Based on this standard training program twice per week, 60 minutes per session, participants will receive an additional 30 minutes (exclude set-up time) of robotic-assisted body weight supported treadmill training (BWSTT) or control training based on their group allocation 3 times for 8 week. EMG biofeedback system will be applied to bilateral vastus lateralis muscles during training with audio feedback to promote active participation. Outcome measures will be collected before the intervention and the subjects will be reassessed after finishing their 8 weeks of intervention. Outcome measures include Walking Index for Spinal Cord Injury version II, Spinal Cord Independence Measure version III, lower extremity motor score, Modified Ashworth Scale, L-stiff and L-force measured by Lokomat system, VO2 maximum, spirometry, and gait analysis (walking speed, heel-heel base support,bilateral stance duration, bilateral symmetry) The result of this study will provide useful information to enhance the clinical effectiveness of the management for spinal cord injury with the use of robotic assisted body weight supported treadmill training.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury
Keywords
Spinal cord injury, robotic, locomotion

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Robotic-assisted body weight supported treadmill training
Arm Type
Active Comparator
Arm Description
Robotic assisted body weight supported treadmill training with conventional PT training
Arm Title
Passive lower limbs mobilization training
Arm Type
Placebo Comparator
Arm Description
Passive lower limbs mobilization training with conventional PT training
Intervention Type
Device
Intervention Name(s)
Robotic-assisted body weight supported treadmill training (Lokomat V6, Hocoma AG, Switzerland)
Intervention Type
Device
Intervention Name(s)
Passive lower limbs mobilization training (Motomed Vivo 2, RECK, Germany)
Primary Outcome Measure Information:
Title
Change in Walking Index for Spinal Cord Injury version II from baseline to 8 weeks
Description
A validated mobility independence assessment tool for spinal cord injury (SCI) population (Burns, Delparte, Patrick, Marino, & Ditunno, 2011). Subjects will be asked to walk on a 10-meter straight line and score will be given based on the use of walking aids, orthoses, manual assistance and distance covered.
Time Frame
Baseline, 8 weeks
Other Pre-specified Outcome Measures:
Title
Change in Spinal Cord Independence Measure version III from baseline to 8 weeks
Description
A validated assessment tool for SCI patients (Catz et al., 2007) to measure performance in different aspects, including self-care ability, respiratory and sphincter management and mobility.. For self-care and respiratory & sphincter domain, scoring will be given based on patient's subjective report while the mobility performance will be tested by the assessors.
Time Frame
Baseline, 8 weeks
Title
Change in lower extremity motor score from baseline to 8 weeks
Description
The sum of muscle power of the 5 key muscles of lower limb. Manual muscle testing will be adopted in testing the muscle power and the grading will be based on the Medical Research Council scale for muscle strength.
Time Frame
Baseline, 8 weeks
Title
Change in Modified Ashworth Scale from baseline to 8 weeks
Description
Hip and knee flexors and extensors will be tested. Subjects will be asked to relax during lying supine and assessor will passively move the limbs in fast speed. Scoring will be given based on the occurrence and quality of resistance.
Time Frame
Baseline, 8 weeks
Title
Change in L-force from baseline to 8 weeks
Description
Strength will be assessed by L-force function which is installed in Lokomat system. subjects will be asked to perform isometric muscle contraction of hips and knees, the sensors in orthoses will measure the force exerted on it and record the result.
Time Frame
Baseline, 8 weeks
Title
Change in walking quality from baseline to 8 weeks
Description
Walking speed, heel-heel base of support, bilateral legs stance duration and bilateral symmetry will be assessed by gait analysis system (GAITRite System, CIR Systems, Inc., US) . Subjects will be asked to walk on a pressure-detectable walkway, which is connected to a computer system. Assistance as well as orthoses will be provided based on subject's own choice. Two meters of acceleration distance will be provided before the subject walk onto the walkway while another two meters of deceleration distance will be provided so as to ensure that subjects walk with their fastest comfortable speed on the whole track of walkway. Bilateral symmetry will be assessed by the stride length ratio as well as stance phase duration ratio of the weak limb to strong limb, where the strong limb is defined as the one with higher score in lower extremity motor score.
Time Frame
Baseline, 8 weeks
Title
Change in maximal oxygen consumption from baseline to 8 weeks
Description
For cardiopulmonary functioning, the subject will be asked to perform upper limb ergometry (Endorphin's 300 e2 resistance system, Endorphin Corporation, US) with a gas analysis system (Fitmate pro, COSMED, Italy). Subjects will wear a mask connecting to the gas analysis system and they will be asked to perform the upper limb ergometry with the following protocol: 1 minute of rest following with 1 minute of warm-up using the least resistance, then the resistance will be increased by 1 level per 1 minute time. The test will be stopped when the heart rate reaches 85% of maximal heart rate, or the subject cannot further tolerate the test. Maximal oxygen consumption will be recorded for further analysis.
Time Frame
Baseline, 8 weeks
Title
Change in L-stiff from baseline to 8 weeks
Description
Stiffness will be assessed by L-stiff function, which subjects will be asked to keep relaxing on the system while the Lokomat system performs passive limbs movement at different speed. The torque during movement will be detected by the sensors in the orthoses and recorded the result.
Time Frame
Baseline, 8 weeks
Title
Spirometry
Description
Spirometry will be used to assess the respiratory function of subjects. Subjects will be asked to perform a forced and prolonged expiration via mouth piece which connecting to a spirometer (Pony FX, COSMED, Italy) followed with a forced inspiration. A soft clip will be applied to subject's nose to minimize air leak from nose during test. Peak expiratory flow (PEF), forced expiratory flow rate in first second (FEV1) and forced vital capacity (FVC) will be assessed. 3 trials will be performed with 1 minute rest interval to prevent hyperventilation and the average value of the 3 trials will be recorded for analysis.
Time Frame
Baseline, 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult patient with age 18 or above suffering from incomplete spinal cord injury with classification B, C or D under the International Standards for Neurological Classification of Spinal Cord Injury (ISNSCI) lesion level above or at T12; acquired the injury not more than 24 months at the time of recruitment traumatic or non-traumatic, non-progressive lesion able to tolerate standing on tilt-table in 90 degrees for more than 30 minutes able to walk with or without orthosis but requires manual assistance in walking. Exclusion Criteria: fracture of spine or lower limbs which is not yet stabilized severe osteoporosis or at high risk of pathological fracture symptomatic postural hypotension; cardiac disease which is not recommended for moderate intensity exercise severe muscle spasticity over lower limbs severe lower limbs fixed contractures leg length discrepancy for more than 2 centimeters body weight exceeding 135 kilograms
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cheung Yu Yeung E, BSc
Organizational Affiliation
Kowloon Hospital, Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Physiotherapy Department, Kowloon Hospital
City
Hong Kong
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
31234791
Citation
Cheung EYY, Yu KKK, Kwan RLC, Ng CKM, Chau RMW, Cheing GLY. Effect of EMG-biofeedback robotic-assisted body weight supported treadmill training on walking ability and cardiopulmonary function on people with subacute spinal cord injuries - a randomized controlled trial. BMC Neurol. 2019 Jun 24;19(1):140. doi: 10.1186/s12883-019-1361-z.
Results Reference
derived

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Robotic-assisted Locomotor Training on Mobility and Cardiopulmonary Function in Patients Suffering From Spinal Cord Injury

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