- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07379099
Implementation of the Personalized Care Plan (PCP) Proposed at the End of Step 2 of the ICOPE Program (INEPPS)
January 23, 2026 updated by: MSPU de Pins-Justaret
Implementation of the Personalized Care Plan (PCP) Proposed at the End of Step 2 of the ICOPE Program : Description of the Procedures for Negotiating the PCP With the Patient, the Procedures for Implementing the PCP in a Multi-professional Setting, and Implementation of the PCP at 1 Year
The ICOPE (Integrated Care for the Elderly) program is based on an integrated approach including a personalized care plan (PCP).
Negotiation methods with the patient and interprofessional cooperation could be key elements in the success of this program.
The main objective is to evaluate the feasibility of the implementation of the ICOPE program on the number and content of the PCP carried out at 1 year
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
600
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Bruno Chicoulaa
- Phone Number: 0033661614449
- Email: bruno1.chicoulaa1@dumg-toulouse.fr
Study Locations
-
-
-
Toulouse, France, 31300
- Recruiting
- Maison de santé des Fontaines
-
Contact:
- Antoine Cabrol, Dr
- Phone Number: 0033561499090
- Email: antoine.cabrol@dumg-toulouse.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Older adults aged 60 years and above, functionally independent
Description
Inclusion Criteria:
- Age ≥ 60 years
- ADL ≥ 5.5
- Affiliated or beneficiary of a social security scheme or equivalent.
- having completed a STEP 2 ICOPE
- not opposed to the collection of their data
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of PCP completed
Time Frame: At 12 months
|
Proportion of personalized care plan (PCP) completed
|
At 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2024
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
April 1, 2028
Study Registration Dates
First Submitted
January 23, 2026
First Submitted That Met QC Criteria
January 23, 2026
First Posted (Actual)
January 30, 2026
Study Record Updates
Last Update Posted (Actual)
January 30, 2026
Last Update Submitted That Met QC Criteria
January 23, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- INEPPS
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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