Robotic-assisted Locomotor Training on Mobility and Cardiopulmonary Function in Patients Suffering From Spinal Cord Injury
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|ClinicalTrials.gov Identifier: NCT01989806|
Recruitment Status : Completed
First Posted : November 21, 2013
Last Update Posted : January 28, 2019
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.
|Condition or disease||Intervention/treatment||Phase|
|Spinal Cord Injury||Device: Robotic-assisted body weight supported treadmill training (Lokomat V6, Hocoma AG, Switzerland) Device: Passive lower limbs mobilization training (Motomed Vivo 2, RECK, Germany)||Not Applicable|
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.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||16 participants|
|Intervention Model:||Parallel Assignment|
|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 Start Date :||December 2013|
|Actual Primary Completion Date :||July 2015|
|Actual Study Completion Date :||July 2015|
Active Comparator: Robotic-assisted body weight supported treadmill training
Robotic assisted body weight supported treadmill training with conventional PT training
Device: Robotic-assisted body weight supported treadmill training (Lokomat V6, Hocoma AG, Switzerland)
Placebo Comparator: Passive lower limbs mobilization training
Passive lower limbs mobilization training with conventional PT training
Device: Passive lower limbs mobilization training (Motomed Vivo 2, RECK, Germany)
- Change in Walking Index for Spinal Cord Injury version II from baseline to 8 weeks [ Time Frame: Baseline, 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.
- Change in Spinal Cord Independence Measure version III from baseline to 8 weeks [ Time Frame: Baseline, 8 weeks ]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.
- Change in lower extremity motor score from baseline to 8 weeks [ Time Frame: Baseline, 8 weeks ]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.
- Change in Modified Ashworth Scale from baseline to 8 weeks [ Time Frame: Baseline, 8 weeks ]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.
- Change in L-force from baseline to 8 weeks [ Time Frame: Baseline, 8 weeks ]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.
- Change in walking quality from baseline to 8 weeks [ Time Frame: Baseline, 8 weeks ]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.
- Change in maximal oxygen consumption from baseline to 8 weeks [ Time Frame: Baseline, 8 weeks ]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.
- Change in L-stiff from baseline to 8 weeks [ Time Frame: Baseline, 8 weeks ]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.
- Spirometry [ Time Frame: Baseline, 8 weeks ]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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01989806
|Physiotherapy Department, Kowloon Hospital|
|Hong Kong, China|
|Principal Investigator:||Cheung Yu Yeung E, BSc||Kowloon Hospital, Hong Kong|