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Robot-assisted Gait Training in Patients With Parkinson's Disease

Primary Purpose

Parkinson Disease

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Robot-assisted gait training
Intensive treadmill training
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease focused on measuring Parkinson Disease, Gait, Balance, Rehabilitation, Robot-assisted gait training

Eligibility Criteria

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

Inclusion Criteria:

  • Clinically confirmed patients with idiopathic Parkinson's disease
  • Hoehn & Yahr stage 2.5 or 3 patients
  • Patients with a Mini-Mental Status Examination (MMSE) score of 24 or higher

Exclusion Criteria:

  • Patients with severe dyskinesia or on-off fluctuations due to medication
  • Patients who need to change drugs during the study period
  • Patients with sensory abnormalities of the lower limb
  • Patients with vestibular disease or paroxismal vertigo
  • Patients with other neurological or orthopedic disease involving legs, or severe cardiovascular diseases

Sites / Locations

  • Seoul National University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Robot-assisted gait training

Intensive treadmill training

Arm Description

Robot-assisted gait training using an exoskeletal robot (Walkbot_S; P&S Mechanics Co. Ltd., Seoul, Korea)

Intensive treadmill training using an usual treadmill

Outcomes

Primary Outcome Measures

10 meter walk test (sec) : single task

Secondary Outcome Measures

10 meter walk test (sec) : single task
10 meter walk test (sec) : cognitive dual-task
10 meter walk test (sec) : physical dual-task
Berg balance scale
The Berg balance scale is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function (Maximum score 56).
Timed-up & go test (sec)
Korean version of Falls Efficacy Scale-International
The FES-I is a 16-item questionnaire of fall-related self-efficacy. The 16 items of the FES-I are rated according to "how concerned you are about the possibility of falling", using the following responses (score in parentheses): not at all (1), somewhat (2), fairly (3), and very concerned (4). Thus, the total score ranges from 16 to 64 points.
New Freezing of Gait questionnaire (NFOG-Q) - Part I
Part I detected the presence of FOG using a dichotomous item in which individuals were classified as a freezer (FR) or a non-freezer (NFR) if they had experienced FOG-episodes during the past month.
New Freezing of Gait questionnaire (NFOG-Q) - Part II, III
Parts II and III were designed for FRs only, providing a total summed score between 0 and 28. Part II (items 2-6, scoring range 0-19) rated the severity of FOG based on its duration and frequency in its most common manifestation, i.e. during turning and initiation of gait. Part III rated the impact of FOG on daily life (items 7-9, scoring range 0-9). No separate on and off rating of parts II and III was considered to avoid unreliable assessment.
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part I
Part I - Non-motor experiences of daily living, questionnaire
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part II
Part II - Motor experiences of daily living, questionnaire
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part III
Part III - Motor examination, structured physical examination
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part IV
Part IV - Motor complications, questionnaire
Functional connectivity in resting-state fMRI (Correlation coefficient)
Correlation coefficient between BOLD signals in motor network At least 6 minutes resting state fMRI imaging is desirable for acquiring stable resting state brain imaging data. The investigators divide the entire brain into voxels, and if the investigators assume TR=3sec, one voxel has 120 time series data. This data reflects the blood-oxygenation level dependent (BOLD) signal, which is related to neural activity via a complex interplay of cerebral blood flow, blood volume, and metabolic rate of oxygen.

Full Information

First Posted
March 21, 2018
Last Updated
December 2, 2019
Sponsor
Seoul National University Hospital
Collaborators
National Rehabilitation Center, Seoul, Korea
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1. Study Identification

Unique Protocol Identification Number
NCT03490578
Brief Title
Robot-assisted Gait Training in Patients With Parkinson's Disease
Official Title
Effect of Robot-assisted Gait Training in Patients With Parkinson's Disease: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
April 23, 2018 (Actual)
Primary Completion Date
November 14, 2019 (Actual)
Study Completion Date
November 14, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
Collaborators
National Rehabilitation Center, Seoul, Korea

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Robot-assisted gait training can improve gait ability of patients with Parkinson's disease by repeating a normal gait pattern with high intensity. This study is a randomized controlled trial to investigate the effect of robot-assisted gait training on walking ability and functional connectivity of brain in patients with Parkinson's disease using an exo-skeletal robot.
Detailed Description
Parkinson's disease is a disease caused by dopamine deficiency in the striatum resulting from the loss of dopaminergic neuronal cells in the cerebral substantia. It is a progressive neurodegenerative disease characterized by motor symptoms including gait disturbance and balance instability. In the early stages of Parkinson's disease, dysfunction of the sensorimotor area of the basal ganglia typically occurs, leading to habitual control hurdles. Accordingly, cognitive efforts are required to perform habitual tasks such as walking, and the automaticity of walking is reduced. Walking performance in a dual-task condition has been used to assess gait automaticity in patients with Parkinson's disease. Patients with Parkinson's disease are known to exhibit changes in functional connectivity of the brain from an early stage. In addition, a number of studies have reported that patients with Parkinson's disease with gait freezing have a change in resting brain activity and functional connectivity of the brain. However, no studies have examined the functional connectivity of the brain in patients with Parkinson's disease before and after rehabilitation. Robot-assisted gait training is a method of rehabilitation that repeats normal gait patterns at high intensity. Recent meta-analysis has shown that robot-assisted gait training improved the recovery of independent gait after stroke compared with conventional rehabilitation therapy. On the other hand, robot-assisted gait training in Parkinson's disease has been reported to improve walking speed and walking endurance compared to conventional physical therapy, but is not superior to treadmill exercise of the same intensity. In addition, it has been reported that in patients with Parkinson's disease with balance impairment, robot-assisted gait training can improve balance disorder compared with physical therapy, and gait freezing has improved in some small-scale patients. However, studies on the effectiveness of robot-assisted gait training in Parkinson's disease are still lacking, and the mechanism of the effect has not been elucidated. In particular, the effect on gait automaticity, which is a characteristic of Parkinson 's disease, and functional connectivity of the brain has not been studied. Therefore, this study is aimed to investigate the effect of robot-assisted gait training on walking ability and functional connectivity of brain in patients with Parkinson's disease using an exo-skeletal robot.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Parkinson Disease, Gait, Balance, Rehabilitation, Robot-assisted gait training

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomized controlled trial
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Robot-assisted gait training
Arm Type
Experimental
Arm Description
Robot-assisted gait training using an exoskeletal robot (Walkbot_S; P&S Mechanics Co. Ltd., Seoul, Korea)
Arm Title
Intensive treadmill training
Arm Type
Active Comparator
Arm Description
Intensive treadmill training using an usual treadmill
Intervention Type
Device
Intervention Name(s)
Robot-assisted gait training
Intervention Description
Patients should use their belts (Harness) to support their weight when walking in equipment. In the first training session, the patient focuses on fitting and adapting the equipment and helps the patient learn. To minimize skin damage, the patient can wear a protector. The initial walking speed starts at 1.0 km/h and can be increased gradually to 3.0 km/h. The gait robot provides an auditory feedback according to gait cycle and a visual feedback on the patient's active participation. If the patient can tolerate, the gait robot may control the walking speed automatically according to the patient's participation. The treatment time per session is 45 minutes including don and doff time. Total 12 sessions are provided for 4 weeks.
Intervention Type
Device
Intervention Name(s)
Intensive treadmill training
Intervention Description
Patients exercise on the treadmill. The initial walking speed starts at 1.0 km/h and can be increased gradually to 3.0 km/h. The therapist provides appropriate visual and auditory instructions to allow the patient to participate in the treadmill training. The treatment time per session is 45 minutes including warm-up and cool-down. Total 12 sessions are provided for 4 weeks.
Primary Outcome Measure Information:
Title
10 meter walk test (sec) : single task
Time Frame
at 4 weeks
Secondary Outcome Measure Information:
Title
10 meter walk test (sec) : single task
Time Frame
baseline, at 8 weeks
Title
10 meter walk test (sec) : cognitive dual-task
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
10 meter walk test (sec) : physical dual-task
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Berg balance scale
Description
The Berg balance scale is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function (Maximum score 56).
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Timed-up & go test (sec)
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Korean version of Falls Efficacy Scale-International
Description
The FES-I is a 16-item questionnaire of fall-related self-efficacy. The 16 items of the FES-I are rated according to "how concerned you are about the possibility of falling", using the following responses (score in parentheses): not at all (1), somewhat (2), fairly (3), and very concerned (4). Thus, the total score ranges from 16 to 64 points.
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
New Freezing of Gait questionnaire (NFOG-Q) - Part I
Description
Part I detected the presence of FOG using a dichotomous item in which individuals were classified as a freezer (FR) or a non-freezer (NFR) if they had experienced FOG-episodes during the past month.
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
New Freezing of Gait questionnaire (NFOG-Q) - Part II, III
Description
Parts II and III were designed for FRs only, providing a total summed score between 0 and 28. Part II (items 2-6, scoring range 0-19) rated the severity of FOG based on its duration and frequency in its most common manifestation, i.e. during turning and initiation of gait. Part III rated the impact of FOG on daily life (items 7-9, scoring range 0-9). No separate on and off rating of parts II and III was considered to avoid unreliable assessment.
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part I
Description
Part I - Non-motor experiences of daily living, questionnaire
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part II
Description
Part II - Motor experiences of daily living, questionnaire
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part III
Description
Part III - Motor examination, structured physical examination
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPRDS) - Part IV
Description
Part IV - Motor complications, questionnaire
Time Frame
baseline, at 4 weeks, at 8 weeks
Title
Functional connectivity in resting-state fMRI (Correlation coefficient)
Description
Correlation coefficient between BOLD signals in motor network At least 6 minutes resting state fMRI imaging is desirable for acquiring stable resting state brain imaging data. The investigators divide the entire brain into voxels, and if the investigators assume TR=3sec, one voxel has 120 time series data. This data reflects the blood-oxygenation level dependent (BOLD) signal, which is related to neural activity via a complex interplay of cerebral blood flow, blood volume, and metabolic rate of oxygen.
Time Frame
baseline, at 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinically confirmed patients with idiopathic Parkinson's disease Hoehn & Yahr stage 2.5 or 3 patients Patients with a Mini-Mental Status Examination (MMSE) score of 24 or higher Exclusion Criteria: Patients with severe dyskinesia or on-off fluctuations due to medication Patients who need to change drugs during the study period Patients with sensory abnormalities of the lower limb Patients with vestibular disease or paroxismal vertigo Patients with other neurological or orthopedic disease involving legs, or severe cardiovascular diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Han Gil Seo, MD, PhD
Organizational Affiliation
Seoul National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
ZIP/Postal Code
03080
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
34896605
Citation
Kim H, Kim E, Yun SJ, Kang MG, Shin HI, Oh BM, Seo HG. Robot-assisted gait training with auditory and visual cues in Parkinson's disease: A randomized controlled trial. Ann Phys Rehabil Med. 2022 May;65(3):101620. doi: 10.1016/j.rehab.2021.101620. Epub 2022 Feb 23.
Results Reference
derived
PubMed Identifier
30616685
Citation
Kang MG, Yun SJ, Shin HI, Kim E, Lee HH, Oh BM, Seo HG. Effects of robot-assisted gait training in patients with Parkinson's disease: study protocol for a randomized controlled trial. Trials. 2019 Jan 7;20(1):15. doi: 10.1186/s13063-018-3123-4. Erratum In: Trials. 2020 May 27;21(1):438.
Results Reference
derived

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Robot-assisted Gait Training in Patients With Parkinson's Disease

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