Comparison of Robot-assisted Gait Training According to Gait Speed in Participants With Stroke

June 18, 2019 updated by: Joon-Ho Shin, National Rehabilitation Center, Seoul, Korea
Comparison of the experimental group that applied the speed of the robot-assisted gait training constantly and the control group that applied the gradual increase of the speed of the robot-assisted gait training.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Unknown

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Anticipated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
20

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

19 years to 80 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Hemiplegic patients secondary to first cerebrovascular accidents
  • Functional ambulation category score ≥ 3

Exclusion Criteria:

  • History of surgery of affected lower limb
  • Fracture of affected lower limb

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
EXPERIMENTAL: Constant gait speed group
experimental group that applied the speed of the robot-assisted gait training constantly
Other: Constant gait speed group
The speed of the robot-assisted gait treatment is constantly applied for 5 times a week for 2 weeks.
OTHER: Increasing gait speed group
control group that applied the gradual increase of the speed of the robot-assisted gait training
Other: Increasing gait speed group
The speed of the robot-assisted gait treatment is gradually increase for 5 times a week for 2 weeks.

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Energy expenditure (EE)
Time Frame: 2 weeks after baseline
EE(kcal/min): energy expenditure per minute
2 weeks after baseline

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Energy expenditure (EE)
Time Frame: baseline, 1 weeks after baseline, 3 weeks after baseline
EE(kcal/min): energy expenditure per minute
baseline, 1 weeks after baseline, 3 weeks after baseline
Heart rate (HR)
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Cardiac frequency
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Volume of Oxygen (VO2)
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
O2 consumption/1min
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Respiratory Quotient (R)
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Respiratory quotient
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Metabolic equivalent (METS)
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
the amount of oxygen consumed while sitting at rest and is equal to 3.5 ml O2 per kg body weight x min
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
oxygenated hemoglobin (OxyHb)
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
oxygenated hemoglobin concentration of cortical activation
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
deoxygenated hemoglobin (DeoxyHb)
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
deoxygenated hemoglobin concentration of cortical activation
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Lower extremity Fugl-Meyer Assessment
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Fugl-Meyer Assessment uses to examine the motor function and coordination of affected lower extremity. It includes 17 items of a 3-point ordinal scale, ranging 0-34, with higher scores indicating lower impairment.
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Functional Ambulation Category
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
Functional Ambulation Category is used to assess gait ability with 6 levels ranging from 0 to 5 on the basis of the amount of physical support required, regardless of use of an assistive device
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
10m walk test
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
10m walk test is used to examine gait speed, in which participant was asked to walk on a 14 meter of walkway wearing harness with two conditions; with the fastest speed or with self-selected comfortable speed.
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
timed up and go test
Time Frame: baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline
simple test used to assess a person's mobility and requires both static and dynamic balance
baseline, 1 weeks after baseline, 2 weeks after baseline, 3 weeks after baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
National Rehabilitation Center, Seoul, Korea

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
July 1, 2019

Primary Completion (ANTICIPATED)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
December 31, 2020

Study Completion (ANTICIPATED)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
December 31, 2020

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
June 18, 2019

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 18, 2019

First Posted (ACTUAL)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
June 19, 2019

Study Record Updates

Last Update Posted (ACTUAL)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
June 19, 2019

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 18, 2019

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
June 1, 2019

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • NRC-2019-01-002

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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