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Motor Imagery Ability After Stroke (AVCIM)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

Stroke

Treatments

Behavioral: Assessment of motor imagery ability of healthy subject
Behavioral: Assessment of motor imagery ability

Study type

Interventional

Funder types

Other

Identifiers

NCT03661073
69HCL18_0059

Details and patient eligibility

About

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.

Enrollment

50 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Stroke
Experimental group
Description:
The investigator will include patients with stroke (either hemorrhagic or ischemic) with or without neglect in the experimental group.
Treatment:
Behavioral: Assessment of motor imagery ability
Healthy subjects
Sham Comparator group
Description:
The investigator will include healthy subjects aged-matched to participants of the experimental group in the control group.
Treatment:
Behavioral: Assessment of motor imagery ability of healthy subject

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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