Reliability, Validity and Responsiveness of the Upright Motor Control Test in Patients With Stroke

March 1, 2022 updated by: Bo-Jhen Chen, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

Impaired motor function is common after stroke. Individuals with stroke often exhibit synergic pattern that disturb daily function. It is crucial to identify the movement impairment in the clinical settings. Upright Motor Control Test (UMCT) is one of the tests developed to assess the selective movement control and functional strength in people with central nervous disorders. It can be used to reflect the impairment of motor function and evaluate changes of performance after treatment. Yet is little to know the clinimetrics of the UMCT on clinical utility. To date, only few researches explore that UMCT has some construct and criterion validity.

Therefore, this study aims to 1) establish the inter-rater reliability to administer the UMCT. 2) explore the correlation between the Fugl-Meyer Assessment of Motor Recovery after Stroke (FMA) and UMCT. 3). investigate whether the UMCT is able to predict the walking ability in patients with stroke.

Study Overview

Status

Terminated

Conditions

Study Type

Observational

Enrollment (Actual)

67

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

      • New Taipei City, Taiwan
        • Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

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

Ages Eligible for Study

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adults with first-ever, unilateral cerebral stroke within one month

Description

Inclusion Criteria:

  • First-ever, unilateral cerebral stroke within one month
  • Being able to maintain standing for more than 10 seconds

Exclusion Criteria:

  • Could not follow commands
  • Deformity or fracture of lower limb
  • Less than 20 years old

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Upright Motor Control Test
Time Frame: 1 month
6-18; higher score means better isolated joint control.
1 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fugl-Meyer Assessment of Motor Recovery after Stroke
Time Frame: 1 month
UE scale:0-66; LE scale:0-34; higher score means better motor function.
1 month

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
10 Meter Walk Test
Time Frame: 1, 3, 6, and 12 month
Test the time required to complete 10 meters of walking.
1, 3, 6, and 12 month
6-Minutes-Waking-Test
Time Frame: 1, 3, 6, and 12 month
Record the distance in six-minute walking.
1, 3, 6, and 12 month
Berg Balance Scale
Time Frame: 1, 3, 6, and 12 month
score: 0-56; lower score means higher risk of fall.
1, 3, 6, and 12 month
Stroke Rehabilitation Assessment of Movement Measure
Time Frame: 1, 3, 6, and 12 month
UE: 0-20; LE: 0-20: Mobility: 0-30; higher score indicated better motor function.
1, 3, 6, and 12 month

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Bo-Jhen Chen, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

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 (Actual)

February 6, 2018

Primary Completion (Actual)

June 30, 2021

Study Completion (Actual)

June 30, 2021

Study Registration Dates

First Submitted

March 14, 2018

First Submitted That Met QC Criteria

March 14, 2018

First Posted (Actual)

March 20, 2018

Study Record Updates

Last Update Posted (Actual)

March 16, 2022

Last Update Submitted That Met QC Criteria

March 1, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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