Parkinson's Disease Trial, Not Yet Recruiting
voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice
Who may and may not be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who may be able to join
- People who have been diagnosed with REM Sleep Behavior Disorder (RBD), confirmed by a sleep study called a polysomnography.
- People who are able to use a smartphone that works with the study's app.
- People who have a care partner (such as a spouse or family member) who shares their bedroom at night.
- Healthy volunteers who are matched in age and sex to the RBD patients enrolled in the trial.
- Healthy volunteers who are able to use a smartphone that works with the study's app.
- Healthy volunteers with no history of RBD.
- People with a confirmed clinical diagnosis of Parkinson's disease (PD) (for a separate confirmation group in the trial).
- People who score between 3 and 12 points on the RBD Screening Questionnaire (for the confirmation group).
- People who do not have dementia (for the confirmation group).
- People who are able to use a smartphone that works with the study's app (for the confirmation group).
- People who have a care partner who shares their bedroom at night (for the confirmation group).
Who may not be able to join
Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.
- People who are not able to give informed consent for the study procedures, as determined by the trial investigator, or who lack the motivation to participate, as determined by the trial investigator.
- People who do not have social security coverage.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Margherita FABBRI, Toulouse Hospital
Phone: 33-561777204
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
This date has passed while the registry still lists the trial as open to participants. Sponsors often update a trial's status without revising its projected end date, so it may well still be recruiting — but the record is out of date in at least one respect. Check with the study contact before relying on either.
Where this trial is recruiting
Primary endpoints
Incidence of nights in a confirmation cohort in which RBD episodes are indicated by a score (digital biomarker) derived from passive actigraphy and photoplethysmography data captured by a smartwatch
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.