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Recruiting NCT06931509

NCT06931509 Integration and Interactions Between Visual and Proprioceptive Feedbacks

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Clinical Trial Summary
NCT ID NCT06931509
Status Recruiting
Phase
Sponsor Centre Hospitalier Universitaire de Saint Etienne
Condition Hemiparetic Stroke
Study Type INTERVENTIONAL
Enrollment 38 participants
Start Date 2025-11-25
Primary Completion 2028-04-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Computerized mirror therapy (IVS3) + Tendon vibration (Vibramoov)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 38 participants in total. It began in 2025-11-25 with a primary completion date of 2028-04-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Mental imagery is a rehabilitation technique for stroke patients, involving the mental representation of movement. Recent technical advancements have enabled the use of visual, proprioceptive, and mixed feedback to enhance motor stimulation. Currently, all post-stroke patients receive these techniques indiscriminately. This study aims to demonstrate differences in the integration of visual and proprioceptive feedback in stroke patients and understand the determinants based on the affected brain area. Patients with motor disabilities will perform motor imagery tasks with various feedback types while their cortical activity is recorded using EEG. EEG data for each type of feedback will be correlated with the lesion area in order to better understand the ongoing mechanisms.

Eligibility Criteria

Inclusion Criteria: * Hemiplegic subjects : Male or female, aged 18 to 80 years, first ischemic or hemorrhagic stroke, having signed the written consent and affiliated or entitled to a social security scheme Exclusion Criteria: * Severe cognitive impairment, severe Aphasia or severe neglect that impair ability to understand instructions or to execute tasks

Contact & Investigator

Central Contact

Diana Rimaud, doctor of science

✉ Diana.Rimaud@chu-st-etienne.fr

📞 0477120467

Principal Investigator

Ahmed Adham, Md

PRINCIPAL INVESTIGATOR

Centre Hospitalier Universitaire de Saint Etienne

Frequently Asked Questions

Who can join the NCT06931509 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Hemiparetic Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06931509 currently recruiting?

Yes, NCT06931509 is actively recruiting participants. Contact the research team at Diana.Rimaud@chu-st-etienne.fr for enrollment information.

Where is the NCT06931509 trial being conducted?

This trial is being conducted at Saint-Etienne, France.

Who is sponsoring the NCT06931509 clinical trial?

NCT06931509 is sponsored by Centre Hospitalier Universitaire de Saint Etienne. The principal investigator is Ahmed Adham, Md at Centre Hospitalier Universitaire de Saint Etienne. The trial plans to enroll 38 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology