Status:

RECRUITING

Brain Mechanisms of Social Perception in Parkinson's Disease

Lead Sponsor:

Hospices Civils de Lyon

Conditions:

Social Perception in Parkinson's Disease

Eligibility:

All Genders

30-75 years

Phase:

NA

Brief Summary

Social cognition is a complex process that enables humans to interpret social information and behave appropriately in a social environment. Social cognition can be impaired in Parkinson's disease pati...

Eligibility Criteria

Inclusion

  • Male or female between 30 and 75 years of age
  • Freely-given informed consent to participate to this study (written form)
  • Affiliated with a social security system or equivalent;
  • Person diagnosed with Parkinson's disease according to MDS-UPDRS criteria for at least 3 years and receiving dopaminergic treatment (e.g. : LEVODOPA, CARBIDOPA, BENZERASIDE, ENTACAPONE, MODOPAR, SINEMET, STALEVO, PRAMIPEXOLE, SIFROL, ROPINIROLE, REQUIP ; ROTIGOTINE, NEUPRO, PIRIBEDIL, TRIVASTAL, RASAGILINE, AZILECT, CONTAM, AMANTADINE, MANTADIX, APOMORPHINE, APOKINON, DOPACEPTIN, FOSLEVODOPA, FOSCARBIDOPA, SCYOVA) (for patients only)
  • Effective contraception for women of childbearing age or post-menopausal women (only for patients and healthy volunteers in stage 2 "imaging")
  • Requiring dopa testing as part of routine care (only for patients in stage 2 "imaging")
  • No disabling cognitive impairment (MOCA score ≥ 26)
  • No diagnosis of chronic disease associated with disability (only for healthy volunteers)

Exclusion

  • Contraindication to MRI (only for patients and healthy volunteers in step 2 "imaging"):
  • Wearing a pacemaker not approved for 3 Tesla MRI
  • Presence of intracerebral ferromagnetic or magnetizable material
  • Presence of intraocular ferromagnetic or magnetizable foreign bodies
  • Presence of non-removable ferro-magnetic or magnetizable foreign bodies in the cephalic region
  • Claustrophobia
  • History of head trauma with loss of consciousness lasting more than 30 min (only for patients and healthy volunteers in step 2 "imaging")
  • Participant not agreeing to be informed in the event of incidental discovery of an abnormality on MRI (only for patients and healthy volunteers in stage 2 "imaging")
  • Tremor or disabling dyskinesias preventing MRI (only for patients in stage 2)
  • Having exceeded the annual amount of compensation allowed for participation in research protocols (only for healthy volunteers)
  • Pregnant, parturient or breast-feeding women
  • Persons deprived of liberty by judicial or administrative decision
  • Persons under psychiatric care
  • Persons admitted to a health or social institution for purposes other than research
  • Adults under legal protection (guardianship, curatorship)
  • Participants in other intervention research involving a period of exclusion still in progress at the time of pre-inclusion.

Key Trial Info

Start Date :

July 15 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

April 1 2027

Estimated Enrollment :

83 Patients enrolled

Trial Details

Trial ID

NCT06884722

Start Date

July 15 2025

End Date

April 1 2027

Last Update

July 22 2025

Active Locations (1)

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Service de neurologie - troubles du mouvement et pathologies neuromusculaires, Hôpital neurologique Pierre Wertheimer/GHE

Bron, France, 69677