Skip to content

Hypnosis During Mechanical Ventilation Weaning

Hypnosis During Mechanical Ventilation Weaning : Feasibility and Physiological Impact

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07518498
Acronym
HYPREA
Enrollment
30
Registered
2026-04-08
Start date
2026-07-01
Completion date
2027-07-01
Last updated
2026-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypnosis, Hypnosis During Weaning From Invasive Mechanical Ventilation, Weaning Mechanical Ventilation

Keywords

Hypnosis, Weaning Mechanical Ventilation, Intensive care unit

Brief summary

Hypnosis is defined as an altered state of consciousness characterized by an increased susceptibility to suggestion. It is a technique commonly used in the medical field, primarily for the management of pain and anxiety. The literature demonstrates that better pain management is correlated with a shorter length of stay in the ICU and a shorter duration of mechanical ventilation. In patients hospitalized in the ICU requiring invasive mechanical ventilation, the emotional component plays a significant role in dyspnea, which can become an obstacle to weaning from ventilation. The analgesic and anxiolytic treatments used carry numerous side effects and contraindications, limiting their use in ICU patients. Furthermore, pulmonary edema is a common cause of failure to wean from invasive mechanical ventilation. By reducing the occurrence of hypertension and tachycardia, hypnosis could be used as a therapeutic strategy to limit its incidence. Thus, hypnosis could be a valuable therapeutic tool for improving tolerance and the success of ventilator weaning. Although hypnosis is already commonly used in intensive care units, its use is still limited by a lack of evidence for more specific indications. It is in this context that this study was conducted, to assess the feasibility of conducting a hypnosis session during weaning from invasive mechanical ventilation in the intensive care unit.

Interventions

BEHAVIORALHypnosis

The intervention consists of a standardized hypnosis session delivered by a trained practitioner during the weaning phase from invasive mechanical ventilation in an intensive care unit.

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER
Centre Hospitalier Régional Metz-Thionville
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 18 and older * Patients hospitalized in the intensive care unit and requiring invasive mechanical ventilation for at least 48 hours * Presence of the prerequisite criteria for ventilator weaning: effective cough, minimal bronchial congestion, patient awake and not agitated, hemodynamic stability (heart rate less than 140 beats per minute, systolic blood pressure between 90 and 160 mmHg without vasopressors), pressure support ventilation, FiO2 \< 40% and PEEP ≤ 8 cmH2O, PaO2/FiO2 \> 150, pH \> 7.35, respiratory rate \< 35 per minute * Patients enrolled in a social security program or eligible for such a program * Patients who has received complete information about the clinical research protocol and has signed an informed consent form * Patients who has undergone a preliminary clinical examination appropriate for the clinical research

Exclusion criteria

* Contraindication to hypnosis (particularly severe psychotic disorders) * Non-French-speaking individuals * Deaf or hard-of-hearing individuals * State of agitation or acute delirium * Individuals who have already undergone a spontaneous ventilation test or an attempt at orotracheal extubation during their hospitalization * Individuals receiving a new anxiolytic or sedative treatment within 2 hours prior to the weaning test * Individuals with a tracheostomy * Women of childbearing age who do not have access to effective contraception * Individuals covered by Articles L. 1121-5, L. 1121-7, and L. 1121-8 of the Public Health Code (pregnant women, women in labor, or breastfeeding women, minors not emancipated, adult subject to a legal protection measure, adult unable to give consent) * Person deprived of liberty by a judicial or administrative decision, or a person receiving psychiatric care pursuant to Articles L. 3212-1 and L. 3213-1

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of a hypnosis session during weaning from invasive mechanical ventilation.At the end of the recruitment periodNumber of hypnosis sessions conducted, relative to the number of eligible patients.

Secondary

MeasureTime frameDescription
Progression of pain and anxiety during weaning from invasive mechanical ventilation using hypnosis.During the hypnosis session (Day 1)Assessment of pain and anxiety using visual analog scales before and after the hypnosis session.
Frequency of failed weaning from invasive mechanical ventilation among patients who underwent a hypnosis session.During ICU stayVentilator weaning failure rate.
Complications associated with weaning from mechanical ventilation using hypnosis.During the ICU stayNumber and types of complications.
Length of stay in the intensive care unit following weaning from mechanical ventilation using hypnosis.ICU stayLength of stay in the intensive care unit.
Mortality following weaning from mechanical ventilation using hypnosis.At day 28Death rate
Patients' experiencesOn the day of discharge from the ICU, and no later than Day 28Form for patients who received hypnosis during weaning from mechanical ventilation.
Professionals' perceptions of hypnosisThroughout the study's enrollment period.Form for healthcare professionals who have conducted at least one hypnosis session.

Countries

France

Contacts

CONTACTSébastien Gibot, MD
s.gibot@chru-nancy.fr+ 33 383851495
STUDY_DIRECTORViviane MARTIN, PhD

The Regional and University Hospital Center of Nancy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 9, 2026