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NCT Number: NCT06059976

HYPNOSIS DURING PERIOPERATIVE CARDIAC SURGERY

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. To evaluate the feelings of patients who received perioperative support using Ericksonian hypnosis during their cardiac surgery treatment.

    Time frame: 1 years

    Perioperative Ericksonian hypnosis satisfaction questionnaire at 6 months and 1 year

Secondary outcomes

  1. 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.

    Time frame: 1 years

    Pain scale: EVS / EVA between 0 and 10

  2. Assessment of stress and anxiety in patients receiving hypnosis at 6 months and 1 year.

    Time frame: 1 years

    EVA anxiety scale, satisfaction questionnaire between 0 and 10

  3. Evaluation of quality of life at 6 months and 1 year.

    Time frame: 1 years

    EQ5D5L questionnaire on a scale between 0 and 100

Study contacts

Contact information is provided by the study sponsor or research team.

Angelina Pollet

CONTACT

[email protected]

0476766729

Delphine Rhem, doctor

CONTACT

[email protected]

04 76 76 67 29

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Registry information

Official study title

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

Acronym: OCEANIC

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Sep 29, 2023
Registry last updated
Jul 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.