Assessing speech intonation after a right-side stroke
Development of a Tool to Assess Receptive Prosody in the Aftermath of a Right Stroke: Use of the Inverse Correlation Paradigm
This project tests a new audio-based method to detect and measure problems with speech intonation (prosody) in adults who had a recent right-hemisphere stroke compared with matched control participants.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris) |
| Trial ID | NCT05874011 on ClinicalTrials.gov |
What this trial studies
The study will apply a data-driven psychoacoustic technique called reverse correlation to uncover how listeners mentally represent prosodic patterns and to quantify perceptual deficits after right supratentorial stroke. Investigators plan a prospective diagnostic cohort of about 150 stroke patients and matched controls to determine whether reverse-correlation measures reliably mark prosodic impairment. Collected patient data will be used for lesion-symptom mapping to relate brain lesions to specific prosodic processing changes. The project also aims to develop a mobile audio-health platform to deliver the test remotely and to provide a day-to-day metric for tracking response to speech therapy.
Who should consider this trial
Good fit: Adults (18+) who are right-handed French native speakers with a first right supratentorial stroke within the past year, able to give informed consent, without dementia or severe dysarthria, and who pass basic comprehension testing (BDAE command score ≥10/15) are ideal candidates.
Not a fit: People with significant language comprehension deficits, known dementia, severe dysarthria, illiteracy, non–French speakers, or those more than one year after their first right-sided stroke are unlikely to benefit or be eligible.
Why it matters
Potential benefit: If successful, this approach could provide a more sensitive diagnostic tool for prosody problems and a portable metric to monitor recovery and guide speech therapy.
How similar studies have performed: Reverse-correlation methods have been used in healthy volunteers and small pilot data in stroke patients are promising, but larger clinical validation is still needed.
Eligibility criteria
Show full inclusion / exclusion criteria
--\>Inclusion Criteria: Inclusion criteria for patients Patient: * with a right supratentorial stroke (1st clinical episode of deficit) confirmed on imaging and less than 1 year old at the time of inclusion * right-handed * male and female over 18 years of age * french mother tongue * affiliated or beneficiary of a social security plan * free, informed and written consent signed * Inclusion criteria for control subjects: Subject: * no known history of stroke * right-handed * over 18 years of age and matched with a case on age (plus or minus 10 years) * french mother tongue * affiliated or beneficiary of a social security plan * free, informed and written consent signed --\>Exclusion Criteria: Non-inclusion criteria for patients and controls subjects * comprehension disorders: score less than 10/15 on the BDAE (Boston Diagnostic Aphasia Examination) command execution test * known dementia * illiteracy * severe dysarthria * psychiatric history requiring hospitalization in a specialized environment for more than two months * history of brain injury * major visual or auditory perceptual disorder (hearing loss greater than 40 dB HL)
Where this trial is running
Paris
- Assistance Publique - Hôpitaux de Paris, Hôpital Pitié-Salpêtrière — Paris, France (Recruiting)
Study contacts
- Principal investigator: Marie VILLAIN, Ms. — Assistance Publique - Hôpitaux de Paris
- Study coordinator: Marie VILLAIN, Ms.
- Email: marie.villain@aphp.fr
- Phone: (0)6 72 34 60 26
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.