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NCT03315273 Clinical Trial

Measuring Motor Imagery Ability in Patients With Traumatic Brain Injury.

Healthy Clinical Trial

Official title:
Measuring Motor Imagery Ability in Patients With Traumatic Brain Injury.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03315273
Other study ID # EC/2017/0826
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 7, 2017
Est. completion date October 30, 2018

Study information
Verified date May 2019
Source University Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

1. Validation of translated Motor Imagery ability questionnaire MIQ-RS

2. Investigating the Motor Imagery ability in patients with traumatic brain injury

Description:

1. Translation of the MIQ-RS following the WHO guidelines. Followed by a validation of this translated questionnaire in patients with traumatic brain injury and in healthy volunteers.

2. Investigating the motor imagery ability using 3 different test

- MIQ-RS (movement imagery questionnaire)

- TDMI (time dependent motor imagery)

- mental chronometry test

Patients and controls will perform all 3 test twice with an interval of 2 weeks to measure the test-retest reliability.

Recruitment information / eligibility
Status Completed
Enrollment 49
Est. completion date October 30, 2018
Est. primary completion date October 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- TBI minimum 3 months ago and maximal 1 year ago

Exclusion Criteria:

- Other neurological disorders

- Severe cognitive deficits, unable to understand the study protocol

- Severe motor impairment, unable to perform the TDMI (Time Dependent Motor Imagery) screening test

Control group:

Matched for age, sex and educational level No neurological disorders present

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Test battery to measure the motor imagery ability
Participants will perform 3 different tests to measure the motor imagery ability

Locations
Country Name City State
Belgium Ghent University Hospital Ghent

Sponsors (2)
Lead Sponsor Collaborator
University Ghent University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Motor imagery ability Results of test battery assessing motor imagery ability 2 assessments with an interval of 2 weeks
Primary Validity translated MIQ-RS Validity of the translated MIQ-RS in patients with traumatic brain injury and healthy volunteers 2 assessments with an interval of 2 weeks
Secondary Test-retest reliability Test- retest reliability of the motor imagery ability test battery 2 assessments with an interval of 2 weeks
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