HYPNOSIS DURING PERIOPERATIVE CARDIAC SURGERY

Recruiting

• Conditions: Hypnosis With Cardiac Surgery

• Registration Number: NCT06059976
• Lead Sponsor: University Hospital, Grenoble

Brief Summary

Evaluation of practices: retrospective and prospective monocentric survey on the satisfaction of patients undergoing Cardiac Surgery who were able to benefit from additional management by Ericksonian Medical Hypnosis during their stay.

Detailed Description

Since 2018, additional care using Ericksonian Medical Hypnosis has been offered to patients undergoing cardiac surgery. Cardiac surgery is one of the most complex and high-risk procedures, requiring a general anaesthetic and a stay in intensive care.

Its aim is to reduce pre-operative stress and anxiety, which are always present to varying degrees before this type of treatment. The aim is to put the patient back at the centre of his or her care by making them active and active participants throughout the treatment process.

Many studies have demonstrated the benefits of hypnosis in reducing anxiety, depression, pain perception, sedation and comfort during hospitalisation. However, very few studies have looked at the quality of life of these patients for up to a year.

Hypnosis support is subject to the number and presence of trained nursing staff.

In order to assess the feelings of patients who have benefited from this additional treatment, and to improve our practices, we would like to carry out a satisfaction survey using questionnaires including the EQ5D-5L quality of life questionnaire.

Study Timeline

• Study Start: 2023-06-01
• Study First Submitted: 2023-09-19
• Study First Submitted QC: 2023-09-26
• Study First Posted: 2023-09-29
• Status Verified: 2024-07
• Last Update Submitted: 2024-07-15
• Last Update Posted: 2024-07-16
• Primary Completion: 2025-06-30
• Study Completion: 2025-12-30

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• > 18 years
• Patients undergoing major cardiac surgery
• Patients who have had perioperative hypnosis sessions.

Exclusion Criteria

• Opposition of the patient to the conservation of data
• Subject under guardianship or subject deprived of liberty, as referred to in articles L1121-5 to L1121-8 of the CSP (French Public Health Code)
• Pregnant or breast-feeding women
• Contraindication to the practice of hypnosis

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To evaluate the feelings of patients who received perioperative support using Ericksonian hypnosis during their cardiac surgery treatment.	1 years	Perioperative Ericksonian hypnosis satisfaction questionnaire at 6 months and 1 year

Secondary Outcome Measures

Name	Time	Method
Evaluation of quality of life at 6 months and 1 year.	1 years	EQ5D5L questionnaire on a scale between 0 and 100
Assessment of pain in patients receiving hypnosis sessions in cardiac surgery on the day of discharge from hospital, at 6 months and at 1 year.	1 years	Pain scale: EVS / EVA between 0 and 10
Assessment of stress and anxiety in patients receiving hypnosis at 6 months and 1 year.	1 years	EVA anxiety scale, satisfaction questionnaire between 0 and 10

Trial Locations

Locations (1)

Delphine Rhem; 🇫🇷 Grenoble, France