Skip to main content
Clinical Trials/NCT03661073
NCT03661073
Completed
Not Applicable

Comprehensive Assessment of Motor Imagery Ability After Stroke

Hospices Civils de Lyon1 site in 1 country50 target enrollmentJuly 17, 2018
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Hospices Civils de Lyon
Enrollment
50
Locations
1
Primary Endpoint
Score of vividness
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Individuals with stroke may experience sensory-motor deficit and/or neglect, with possible reduction in motor imagery ability (MI). To our knowledge, no study completely investigated MI ability in one individual whereas MI practice can be performed using visual or kinesthetic modalities (respectively visualizing with mind's eyes or imagining movement using sensation) and internal or external perspectives (performing action as spectator or as actor). This study aims to investigate MI ability in patients with stroke as compared to aged-matched healthy individuals. The investigators will assess explicit MI ability using 3 questionnaires (Movement Imagery Questionnaire-RS - MIQ-RS, Kinesthetic and Visual Imagery Questionnaire-20 - KVIQ-20, Vividness of Movement Imagery Questionnaire-2 - VMIQ-2) and 2 tests (imagined Time Up and Go - iTUG, imagined Box and Block test - iBBT). Outcome parameters will be i) the composite score of vividness measured for all tests using Likert scales, ii) the temporal equivalence between MI and Physical practice (PP - where MI/PP ratio equal to 1 indicate good MI ability and respect of temporal equivalence between MI and PP) and iii) the amplitude of electrodermal activity. The investigators will also study implicit MI ability using a hand laterality judgment task. Outcomes parameters will be response time (i.e. the duration to identify the hand laterality) and the percentage of correct responses.

Registry
clinicaltrials.gov
Start Date
July 17, 2018
End Date
January 17, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • For both groups:
  • be more than 18 years old
  • be less than 75 years old
  • benefit from social security
  • For experimental group:
  • patient admitted in Henry Gabrielle hospital for rehabilitation
  • patient with one single episode of stroke

Exclusion Criteria

  • For patients:
  • sign of cognitive decline (MMSE score under 27/30)
  • evolutionary pathology associated
  • For healthy subjects:
  • neurological or orthopaedical history

Outcomes

Primary Outcomes

Score of vividness

Time Frame: Day 1

Participants will self-report vividness that describe the success in imagining movements using a 5-points Likert scale (1=no image or no sensation to 5=image as clear as PP or sensation as intense as PP) for the KVIQ-20. The investigators will average the vividness for each items of the questionnaire.

Secondary Outcomes

  • Temporal equivalence measured during KVIQ-20(Day 1)
  • Amplitude of electrodermal responses that will be measured during imagined movement with reference to actual movements measured during VMIQ -2.(Day 1)
  • Amplitude of electrodermal responses that will be measured during imagined movement with reference to actual movements measured during MIQ-RS.(Day 3)
  • Score of vividness measured during iTUG.(Day 5)
  • Temporal equivalence measured during iTUG.(Day 5)
  • Score of vividness measured during MIQ-RS.(Day 3)
  • Response time to identify the hand laterality during the implicit motor imagery ability assessment(Day 3)
  • Amplitude of electrodermal responses that will be measured during imagined movement with reference to actual movements measured during iTUG.(Day 5)
  • Temporal equivalence measured during iBBT.(Day 5)
  • Amplitude of electrodermal responses that will be measured during imagined movement with reference to actual movements measured during KVIQ-20.(Day 1)
  • Score of vividness measured during VMIQ -2(Day 1)
  • Temporal equivalence measured during MIQ-RS.(Day 3)
  • Percentage of correct response to identify the hand laterality during the implicit motor imagery ability assessment(Day 3)
  • Amplitude of electrodermal responses that will be measured during imagined movement with reference to actual movements measured during iBBT.(Day 5)
  • Score of vividness measured during iBBT.(Day 5)

Study Sites (1)

Loading locations...

Similar Trials