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Studying Hand Sensation and Movement Recovery After Stroke Using Brain Scans

Tests hand sensing and movement tools, plus brain scans, in adults recovering from stroke.

Plain-language title generated from the registry record
Registry title: Sensory Mechanisms of Manual Dexterity Recovery After Stroke: a Prospective Cohort Study of Prediction and Cerebral Correlates

Key facts

Where
Paris, FranceSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 85 years old?

Source: NCT07340736, who can take part

Where in France

  • GHU Psychiatrie et NeurosciencesParis, FranceNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Centre Hospitalier St Anne
Trial code
NCT07340736
Record updated
14 January 2026
Original description
In the proposed research, we will assess motor and sensory functions of the hand using clinical tests and a tool designed to measure manual dexterity combined with vibrotactile stimulation. We will also evaluate the integrity of brain structure and function using MRI.Read full original descriptionShow less

Sensory Mechanisms of Manual Dexterity Recovery After Stroke: a Prospective Cohort Study of Prediction and Cerebral Correlates

In the proposed research, we will assess motor and sensory functions of the hand using clinical tests and a tool designed to measure manual dexterity combined with vibrotactile stimulation. We will also evaluate the integrity of brain structure and function using MRI.

Inclusion: First symptomatic stroke, ischaemic or haemorrhagic in the early subacute phase (up to 3 weeks post-stroke); Upper limb paresis (≤4/5 MRC Scale); Ability to grasp, lift and put down 1 block (from the BBT test); Be affiliated to a social security.

Exclusion: Contraindications to MRI (claustrophobia, presence of cochlear implants and/or pacemakers); Presence of another neurological or musculoskeletal condition affecting upper limb movement; Severe cognitive impairment and/or aphasia with inability to understand and carry out instructions; Life-threatening conditions or conditions requiring follow-up at 6 months; Epilepsy; Known hypersensitivity or allergy to silicone; Persons subject to legal protection measures; Persons subject to judicial protection measures; Pregnancy.

ClinicalTrials.gov NCT07340736