- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04165915
Seniors'Health Paths " PAERPA ", (PAERPA)
Seniors'Health Paths " PAERPA ", a Support Being Made Available to General Practionners for Assistance in the Management of Elderly Persons at Risk of Losing Their Independence. Review of the Implementation of the Arrangement on the Est-héraultais Territory.
•Background: PAERPA experimentation implemented in the East-Herault region since September 2017 aims to identify fragility and prevent the risk of loss of autonomy in elderly persons older than 60 years by facilitating coordination between Professionals taking care of the patient with the personalized health plan " PPS". The main objective of this study was to evaluate the implementation of this device through the achievement or not of the objectives set by the PPS.
•Methods: Descriptive cohort study with retrospective inclusion and prospective follow-up from the East Herault CTA database. All patients over 60 years old living at home and having a PPS written between September 2017 and April 2018 were included. PPS monitoring for 1 year. Description of this population then analysis of PPS.
•Discussion: Our study aims to evaluate the implementation of the device to identify ways to improve the device for the management of subjects at risk of loss of autonomy.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Montpellier, France, 34295
- Uhmontpellier
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
An individual must fulfill all of the following criteria in order to be eligible for study enrollment:
- Aged of 60 years and more
- individual health care plan was prepared
- living in the Est-Héraultais territory
Exclusion Criteria:
- Hospitalized patients
- Patients who declined to have an individual heath care planPsychosis
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Estimating goals set by the PPS (personalized health plan)
Time Frame: 6 and 12 month follow-up
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achievement of objectives established in the individual health care plan after 6 and 12 month follow-up
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6 and 12 month follow-up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
correlation between unwillingness and cognitive disorder
Time Frame: 1 day
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correlation between unwillingness and cognitive disorder
|
1 day
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Correlation between unwillingness and numbers of established goals
Time Frame: 1 day
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Correlation between unwillingness and numbers of established goals
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1 day
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Correlation between unwillingness and locomotors goals
Time Frame: 1 day
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Correlation between unwillingness and locomotors goals
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1 day
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Chokri Boubakri, MD, University Hospitals of Montpellier
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RECHMPL19_0513
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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