Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
Healthy Volunteers
NCT06080659

Network-based biOmarker Discovery of Neurodegenerative Diseases Using Multimodal Connectivity

Led by Rennes University Hospital · Updated on 2026-01-05

120

Participants Needed

1

Research Sites

160 weeks

Total Duration

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AI-Summary

What this Trial Is About

The aim of the NODAL clinical trial is to demonstrate the feasibility of new, low-cost, non-invasive biomarkers of neurodegenerative pathologies as early Alzheimer and Parkinson, based on the estimation of the multimodal connectome.

CONDITIONS

Official Title

Network-based biOmarker Discovery of Neurodegenerative Diseases Using Multimodal Connectivity

Who Can Participate

Age: 50Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • French mother tongue
  • Right-handed
  • Education level equal to or higher than Primary School Certificate
  • No medical or psychiatric condition likely to affect cognition (except diagnosis for patients)
  • Affiliated with a social security scheme
  • Provided informed consent
  • For subjective cognitive decline-plus group: meets Jessen criteria
  • For Alzheimer's patients with mild cognitive impairment: meets Albert criteria
  • For newly diagnosed Parkinson's patients without cognitive deficits: meets Postuma criteria
  • For Parkinson's patients with mild cognitive impairment: meets Litvan criteria
Not Eligible

You will not qualify if you...

  • MRI contraindications such as abdominal circumference plus upper limbs > 200 cm
  • Having an implantable pacemaker or defibrillator
  • Presence of neurosurgical clips
  • Having cochlear implants
  • Having neural or peripheral stimulators
  • Intra-orbital or brain metallic foreign bodies
  • Recent endoprostheses (<4 weeks) or osteosynthesis devices (<6 weeks)
  • Claustrophobia
  • Pregnant or breastfeeding women
  • Adults under legal protection or deprived of liberty
  • Score >2 on modified Hachinski scale (patients only)
  • Dementia by McKhann criteria (patients only)
  • Sensory deficits interfering with tests (patients only)
  • Cognitive impairment with MoCA score < 26 (healthy volunteers only)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU Rennes

Rennes, France

Actively Recruiting

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Research Team

M

marie-laure gervais, Phd

CONTACT

P

Pierre-Yves JONIN, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

5

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