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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.
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
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Hopital Pellegrin
Bordeaux, France
CHU de Lille
Lille, France
CHU de Limoges
Limoges, France
CHU Poitiers
Poitiers, France
Start Date
December 6, 2022
Primary Completion Date
December 6, 2025
Completion Date
June 6, 2027
Last Updated
July 23, 2025
250
ESTIMATED participants
ESPark Intervention
PROCEDURE
Lead Sponsor
University Hospital, Bordeaux
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT06113640