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Trying out examinations for future research

Researchers test the feasibility of examinations and study procedures before using them in larger research projects.

Testing a treatment or activity · Study reference: NCT05698810

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.

Open the official registry record ↗

Follow this study

Looking for volunteers

Start (reported actual date)
2023-03-20
Main measurements finished (planned)
2033-03-20
Study finished (planned)
2033-03-20

Planned dates can move. A study finishing does not tell us when a paper will be published.

No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Age 18 years and over · Also accepts healthy volunteers

These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.

Read all the rules for taking part

Sex eligibility reported by registry: all

Inclusion Criteria: * Age ⩾ 18 years * Affiliated to a social security scheme * Free and informed consent signed Exclusion Criteria: * Subject in a period of exclusion from another study. * Subject deprived of liberty by a judicial or administrative decision, or major subject subject to a legal protection measure (guardianship, curatorship and safeguarding of justice) referred to in Articles 1121-6 to 1121-8 of the Public Health Code. * Subject who would receive more than 4500 euros in compensation because of his participation in other research involving the human person in the 12 months preceding this study. * Pregnant woman, parturient, nursing mother (Article 1121-5 of the Public Health Code) * Subject not reachable urgently.
Full study name & original research details

Official study title

Preparation and Feasibility of Exams for Expected Studies (PRELUDE)

Short title used by the registry

Preparation and Feasibility of Exams for Expected Studies

Original description

Feasibility study: the examinations carried out as part of this protocol aim to carry out all the acquisitions and simulations of use, necessary for the development of the clinical research protocols to come to Clinatec (in particular, configuration of the equipment, dimension of the examination time and the size of the cohorts etc ...)

Further description from the registry

To ensure the feasibility of a clinical trial, it is necessary to test the parameters as well as the sequence of the different examination times offered to participants. The expected results of this protocol are mainly the dimension of experimental paradigms and the optimization of the clinical management of subjects.

Conditions reported: Healthy Volunteers; Parkinson's Disease Patients; Para/Tetraplegic Patients

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Interventional
Interventions
CE marked Medical Device MagnetoEncephaloGraphy (MEG) usability; CE marked Medical Device Magnetic Resonance Imaging (MRI) usability; CE marked Medical Device ElectroEncephaloGraphy (EEG) usability; CE marked Medical Device ElectroCardioGraphy (ECG) usability
Phases
NA
Sponsor
University Hospital, Grenoble
Start date reported by registry
2023-03-20 (actual)

Registry updated: 2025-09-02 · Status last verified by the registry submitter: 2025-08

Registry records retrieved 2026-10-13 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

No central contact is listed. Check the location contacts or the official registry record.

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

Clinatec Cea/Chuga

Grenoble, France

Recruiting

Stéphan CHABARDES, MD, PhD · +33476767559 · SChabardes@chu-grenoble.fr

Caroline SANDRE-BALLESTER, PhD · 0438782851 · csandreballester@chu-grenoble.fr

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.