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Completed

NCT Number: NCT06786962

Virtual Reality Hypnosis and Nurses' Stress

The practice of nursing is based on helping relationships and empathy. The work is physically, mentally and emotionally demanding. This requires the mobilization of personal resources (lifestyle, coping strategies) and work resources (managerial, medical support, recognition) to cope with stress. When these resources are present, nurses can activate a resilience process through coping strategies. However, stress levels and emotional impact are such that they can lead to states of suffering and trauma such as compassion fatigue (CF). The prevalence of CF is high in the nursing profession and particularly among neonatal intensive care (NICU) nurses.

Several levels of intervention exist to prevent CF in services: organizational, inter-individual and individual. At the individual level, certain interventions such as meditation have been studied, showing positive effects with the highest levels of evidence.

On the other hand, interventions such as hypnosis have not yet been studied in this context. There is, however, an interest in studying hypnosis as a non-pharmacological intervention to reduce stress and improve emotional regulation. Indeed, the hypnotic process (promoting attentional and cognitive rest, redirecting attentional focus, reducing mental effort) is a resource activator. In order to combine individual and organizational support, the intervention must be offered in the workplace and during working hours, given the difficulty nurses have in extracting themselves from the service, the restricted break time and the acceptability of the virtual reality system. In a context where break time is short and precious, it is necessary to use a tool that adapts to these constraints. Virtual reality with the HypnoVR® tool meets these needs. This device acts as a restorative environment. It has already proven its effectiveness in the care of painful and stressed patients in critical situations. It has not yet been studied in the context of work-related stress in healthcare professionals, such as neonatal intensive care nurses. The protocol takes into account the results of studies reporting the effects associated with the use of virtual reality (VR).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

RENNES

Rennes, Brittany Region, 35000, France

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Nurse
  • Regularly work in a neonatal intensive care unit
  • Be of legal age and not opposed to participating in research
  • Fluency in French

Exclusion criteria

  • Age < 18
  • Refusal to participate
  • Current anticonvulsant or psychotropic treatment

Treatment and study plan

Virtual Reality Hypnosis

Device

The experimental group of 22 participants consists of a hypnosis intervention using a virtual reality device (HypnoVR®).

Participants are seated in a quiet area of the unit:

They choose a visual scenario from among 3 proposals, guaranteeing the conditions of a restorative environment. During each session, the same script (support mode) is spoken and the same music (serenity program with soothing tones) is associated with the script. Each participant is fitted with a virtual reality mask and a headset with active noise reduction.

Control arm (SEQ):

Other

Restoration time

Participants are seated in a quiet area of the unit. The control group of 21 participants consists of a break with the following instructions and suggestions:

"Take advantage of this break, this time just for you, to recharge your batteries. Sit in this armchair and I suggest you think of something pleasant and comfortable".

Primary outcomes

  1. Stress levels

    Time frame: From enrollment to the end of treatment at 8 weeks

    Perceived stress: a single question on stress symptoms : "Stress is a situation in which a person feels tense, restless, nervous or anxious, or can't sleep at night because their mind is constantly troubled. Are you feeling this type of stress these days?" The answer will be recorded on a five-point Likert scale ranging from 1 (not at all) to 5 (a lot).

  2. Emotions

    Time frame: From enrollment to the end of treatment at 8 weeks

    Emotions : 10 items from the short version of the Positive and Negative Affects Schedule .

  3. Anxiety

    Time frame: From enrollment to the end of treatment at 8 weeks

    State anxiety : 10 items from the short version of the State Anxiety Scale

  4. Restoration

    Time frame: From enrollment to the end of treatment at 8 weeks

    Restoration: 3 items from the Mental Restoration Scale

  5. Satisfaction and compassion fatigue

    Time frame: From enrollment to the end of treatment at 8 weeks

    Satisfaction and compassion fatigue: 21 items from the ProQOL - 21 scale

  6. Comfort level

    Time frame: From enrollment to the end of treatment at 8 weeks

    Comfort: indicator of parasympathetic changes in emotional situations during each session, with the ANI Guardian® device.

Secondary outcomes

  1. Evaluation of experience

    Time frame: From enrollment to the end of treatment at 8 weeks

    Experience Open-ended question about the user experience during the session ("Your comments on the session"): "How did you experience this session?" Responses will be analyzed using an approach combining inductive coding and content analysis based on hypnosis processes identified in the literature

  2. Acceptability

    Time frame: From enrollment to the end of treatment at 8 weeks

    To assess acceptability, participants will rate their perception of the relaxation activity using five items from the Unified Theory of Acceptance and Use of Technology (UTAUT). These items assess ease of use, usefulness, effectiveness, overall satisfaction and behavioral intention. Participants will respond on a 10-point Likert scale ranging from 1 (strongly disagree) to 10 (strongly agree).

Sponsors and collaborators

Lead sponsor

CARESP: Cellule d'animation régionale en soins palliatifs

Other

Collaborators

  • University of Rennes 2

Registry information

Official study title

Effects of a Virtual Reality Hypnosis Intervention on Reducing Stress and Compassion Fatigue in Neonatal Intensive Care Nurses

Acronym: HYPNOVRNEO

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jan 22, 2025
Registry last updated
Feb 14, 2025

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.

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