Risk Factors for the Occurrence of Post Intensive Care Syndrome (PICS)

NCT ID: NCT05534828

Last Updated: 2024-09-25

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 97 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-10-10
• Study Completion Date: 2023-06-30

Brief Summary

Monocentric, observational, descriptive RIPH3 study with prospective data collection.

Detailed Description

A consultation in the form of a teleconsultation with video conference is proposed to all adult patients who have stayed more than 24 hours in the Rangueil intensive care unit.

This consultation is scheduled and will take place approximately three months after the end of the stay in the intensive care unit.

During this consultation, signs will be sought through questioning to detect or even diagnose the presence of a PICS.

We will also look for elements that will allow us to characterize people with CHIP.

If a PICS was detected during the consultation, the summary letter sent to the attending physician informs him/her of

1. The presence of a CHIP in his patient

2. The nature of this CHIP (CHIP with a purely psychological component, CHIP with a psychological and physical component, etc.) In this same summary letter, the attending physician will be offered a list of specialists practicing at the CHU who are likely to take charge of the patient's CHIP.

Conditions

Post Intensive Care Syndrome

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Interventions

A consultation

A consultation at three months of discharge from the intensive care unit in the population of patients surviving a multivalent intensive care unit stay

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• adult patient
• hospitalized in the intensive care unit of Rangueil of the TOULOUSE University Hospital
• length of stay in intensive care equal or superior to 24 hours
• affiliated to a social security system
• having expressed no objection to participate in the study

Exclusion Criteria

• minor patient
• no consent to the study
• patient not capable of expressing his "non opposition" to the study
• patient under guardianship, curatorship or safeguard of justice

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Toulouse

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University Hospital of Toulouse

Toulouse, , France

Countries

France

Other Identifiers

2022-A01371-42

Identifier Type: OTHER

Identifier Source: secondary_id

RC31/22/0215

Identifier Type: -

Identifier Source: org_study_id