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Trial record 26 of 314 for:    Recruiting, Not yet recruiting, Available Studies | "Brain Injuries, Traumatic"

Measuring Motor Imagery Ability in Patients With Traumatic Brain Injury.

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ClinicalTrials.gov Identifier: NCT03315273
Recruitment Status : Recruiting
First Posted : October 20, 2017
Last Update Posted : November 24, 2017
Sponsor:
Collaborator:
University Hospital, Ghent
Information provided by (Responsible Party):
University Ghent

October 3, 2017
October 20, 2017
November 24, 2017
November 7, 2017
April 30, 2018   (Final data collection date for primary outcome measure)
  • Motor imagery ability [ Time Frame: 2 assessments with an interval of 2 weeks ]
    Results of test battery assessing motor imagery ability
  • Validity translated MIQ-RS [ Time Frame: 2 assessments with an interval of 2 weeks ]
    Validity of the translated MIQ-RS in patients with traumatic brain injury and healthy volunteers
Same as current
Complete list of historical versions of study NCT03315273 on ClinicalTrials.gov Archive Site
Test-retest reliability [ Time Frame: 2 assessments with an interval of 2 weeks ]
Test- retest reliability of the motor imagery ability test battery
Same as current
Not Provided
Not Provided
 
Measuring Motor Imagery Ability in Patients With Traumatic Brain Injury.
Measuring Motor Imagery Ability in Patients With Traumatic Brain Injury.
  1. Validation of translated Motor Imagery ability questionnaire MIQ-RS
  2. Investigating the Motor Imagery ability in patients with traumatic brain injury
  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.

Interventional
Not Applicable
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Intervention Model Description:
Comparison of 2 groups: one existing of patients with traumatic brain injury and one control group of healthy volunteers matched for age, sex and educational level
Masking: None (Open Label)
Primary Purpose: Treatment
  • Traumatic Brain Injury
  • Healthy
Other: Test battery to measure the motor imagery ability
Participants will perform 3 different tests to measure the motor imagery ability
  • Experimental: Traumatic brain injury

    Patients who have suffered a traumatic brain injury will be assessed with a test battery including

    • a motor imagery ability questionnaire (MIQ-rs)
    • a mental rotation test
    • a chronometry test (TDMI)
    Intervention: Other: Test battery to measure the motor imagery ability
  • Active Comparator: Control

    Healthy volunteers matched for age, sex and educational level will be assessed with the same test battery including

    • a motor imagery ability questionnaire (MIQ-RS)
    • a mental rotation test
    • a chronometry test (TDMI)
    Intervention: Other: Test battery to measure the motor imagery ability
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
80
Same as current
September 30, 2018
April 30, 2018   (Final data collection date for primary outcome measure)

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

Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
Yes
Contact: Anke Van Bladel, PT 09/332.46.57 anke.vanbladel@ugent.be
Belgium
 
 
NCT03315273
EC/2017/0826
Not Provided
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Not Provided
University Ghent
University Ghent
University Hospital, Ghent
Principal Investigator: Kristine Oostra, MD University Hospital, Ghent
University Ghent
November 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP