Measuring Motor Imagery Ability in Patients With Traumatic Brain Injury.
NCT ID: NCT03315273
Last Updated: 2019-05-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
49 participants
INTERVENTIONAL
2017-11-07
2018-10-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
2. Investigating the Motor Imagery ability in patients with traumatic brain injury
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Training Cognition With Neurofeedback After Stroke
NCT06852209
Feasibility of a Motor-cognitive Training Program in Patients With Traumatic Brain Injury
NCT06149975
Efficacy of Multidimensional Management of Mild Traumatic Brain Injury
NCT03811626
Perceptual-Cognitive Training After a Mild Traumatic Brain Injury: Towards a Sensitive Marker for Recovery
NCT03213730
The Neural Substrates for Working Memory Training
NCT03012269
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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)
Test battery to measure the motor imagery ability
Participants will perform 3 different tests to measure the motor imagery ability
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)
Test battery to measure the motor imagery ability
Participants will perform 3 different tests to measure the motor imagery ability
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Test battery to measure the motor imagery ability
Participants will perform 3 different tests to measure the motor imagery ability
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* 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
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Ghent
OTHER
University Ghent
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Kristine Oostra, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Ghent
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ghent University Hospital
Ghent, , Belgium
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
EC/2017/0826
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.