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Recruiting NCT07379099

Implementation of the Personalized Care Plan (PCP) Proposed at the End of Step 2 of the ICOPE Program

Observational Frailty Frailty at Older Adults

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Frailty, Frailty at Older Adults. Basic parameters: from 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

Primary outcome measures

  • Proportion of PCP completed [Time frame: At 12 months]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Maison de santé des Fontaines — Toulouse

Identifiers

NCT: NCT07379099 · INEPPS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗