Immersive Sensory Projections for Hospitalized Patients

ConditionHospitalism
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

About this trial

The purpose of this study is to assess the impact of adding three sensory elements (visual, auditory, olfactory) on reducing discomfort in patients hospitalized in the intensive care unit/continuing care unit.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years ;

Patient hospitalized in intensive care or continuing care unit for an estimated minimum of 48 hours;

Patient hospitalized for a medical indication (including in the pre-surgical phase) or in the post-surgical phase;

Patient or support person who speaks and understands French, has understood the research procedures and is able to complete the questionnaires;

Disqualifiers

Deaf or blind patient;

Asthmatic patient with background treatment;

Epileptic patient or known history of convulsion;

Known allergy or intolerance to essential oils or to a component of essential oils;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Hospitalization in intensive care or continuing care unit

    Procedure/Surgery

    Hospitalization in intensive care or continuing care unit for medical reasons or surgery, conscious or unconscious under mechanical ventilation. Resuscitation patients are then cared for in a continuing care unit.

Treatment groups

208 Participants
are divided into 2 treatment groups
Group A: Immersive sensory projectionsExperimental treatment 1 intervention
Group B: No immersive sensory projectionsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

REAnimation Patient Discomfort Questionnaire

Overall score on the REAnimation Patient Discomfort Questionnaire at the end-of-study visit

Time frame
2 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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