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Specialist Parkinson’s care at home

Researchers study care delivered at home by a team of professionals with different areas of expertise in Parkinson’s.

Testing a treatment or activity · Study reference: NCT05433441

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.

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Looking for volunteers

Start (reported actual date)
2022-12-06
Main measurements finished (planned)
2025-12-06
Study finished (planned)
2027-06-06

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: For the patient: * Patient with a diagnosis of idiopathic Parkinson's disease * Patient over 18 years ; * Patient with a Hoehn and Yahr Stage greater than or equal to 3; * Patient without major cognitive impairment defined by a MOCA score ≥21 * Patient living at home ; * Patient with an identified non-professional primary caregiver; * Person affiliated with or benefiting from a social security plan; * Free, informed and and express consent (confirmed in writing) (no later than the day of inclusion and before any examination required by the research). For the caregiver: * Male or female over 18 years * Able to respond to research interviews/questionnaires * Free, informed and express consent (confirmed in writing) (no later than the day of inclusion and before any examination required by the research). Exclusion Criteria: For the patient: * Patient with medically indicated dementia impairing comprehension and adherence, and/or with severe confusion or psycho-hallucinatory state; * Institutionalized or foster care patients; * Patients with a known severe and unstable general pathology that does not allow for patient follow-up; * Patients already included in another non-drug management trial; * Patients whose institutionalization is envisaged in the short term (within 6 months) or for whom a change of residence is envisaged in the short term and would not allow for follow-up assessments; * Patients under guardianship or unable to express consent * Primary caregiver not wishing to participate in the study or unable to be available for the planned study follow-up; * Presence of a primary caregiver with a known severe and unstable disease that does not allow for the conduct of the study; * Presence of a primary caregiver with a known cognitive or psychiatric disorder (chronic progressive psychosis) that does not allow for the proper conduct of the study. * Pregnant or breastfeeding woman. For the caregiver: * Unable to follow the research interviews or questionnaires. * Primary caregiver not wishing to participate in the study or unable to be available for the planned study follow-up; * Primary caregiver with a known severe and unstable illness that does not allow for the proper conduct of the study; * Primary caregiver with known cognitive or psychiatric disorders (chronic progressive psychosis) that do not allow the study to be conducted properly.
Full study name & original research details

Official study title

Evaluation of the Effectiveness of the Parkinson's Specialized Teams Intervention on the Quality of Life of Parkinson's Patients in the Territory of the Nouvelle-Aquitaine and Hauts-de-France: ES-Park Pilot Study.

Short title used by the registry

Evaluation of the Effectiveness of the Parkinson Specialized Teams Intervention

Original description

A pilot experiment interventional study is proposed in order to set up multidisciplinary team for Parkinson's patients at home. The aim of this study is to evaluate the effectiveness of this specialized Parkinson's team (ESPark) intervention a on the quality of life of patients with moderate to severe Parkinson's disease

Further description from the registry

Parkinson's disease (PD) and related disorders are the second most common cause of motor disability in the elderly after stroke. Progressively, the disability impacts the activities of daily living and social life of Parkinson's patients with a major impact on their quality of life. The diversity and complexity of the needs of parkinsonian patients and their caregivers justify a specific multidisciplinary approach. Several studies have evaluated the effectiveness of the intervention of such teams on the maintenance of activities of daily living and quality of life of Parkinson's patients with contradictory results. In France, the experience of specialized Alzheimer teams (ESA) based on the same concept seems to have brought positive results on autonomy and resocialization. Based on the positive experience of ESA intervention in Alzheimer's disease and in view of the data in the literature on Parkinson's disease, we would like to develop the same type of care with teams adapted to the problems of Parkinson's disease patients, which we could call ESParks, and to evaluate the effectiveness of such teams in the context of support for Parkinson's patients.

Conditions reported: Parkinson Disease

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
ESPark Intervention
Phases
NA
Sponsor
University Hospital, Bordeaux
Start date reported by registry
2022-12-06 (actual)

Registry updated: 2025-07-23 · Status last verified by the registry submitter: 2025-07

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.

Alexandra FOUBERT-SAMIER, Dr · 05 57 82 12 53 · alexandra.samier-foubert@u-bordeaux.fr

Sandrine DUPOUY · 05 57 82 14 62 · sandrine.dupouy@chu-bordeaux.fr

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.

Hopital Pellegrin

Bordeaux, France

Recruiting

Alexandra FOUBERT-SAMIER, Dr · alexandra.samier-foubert@u-bordeaux.fr

CHU de Lille

Lille, France

Recruiting

Nicolas CARRIERE, Dr · 0320446752 · nicolas.carriere@chu-lille.fr

CHU de Limoges

Limoges, France

Recruiting

Jean-Luc HOUETO, Pr · jean-luc.houeto@chu-limoges.fr

CHU Poitiers

Poitiers, France

Recruiting

Isabelle BENATRU, Dr · isabelle.benatru@chu-poitiers.fr

Facility not reported

France

Status not reported

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