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Atmospheric Projection in the Emergency Department (AERIAL-MED)

L

Lausanne University Hospital (CHUV)

Status

Terminated

Conditions

Anxiety Acute
Pain, Acute

Treatments

Device: Immersive atmospheric projection
Device: Minimal atmospheric projection

Study type

Interventional

Funder types

Other

Identifiers

NCT05967988
CER-VD 2023-00867

Details and patient eligibility

About

The goal of this clinical trial is to learn about the reduction of pain and anxiety during a minor procedure in the emergency department on adult patients through the visualisation of atmospheric projection as a distraction mean. The main question it aims to answer is :

Can the atmospheric projection of a video reduce pain and anxiety in adult patients receiving painful procedures in the emergency department ?

Participants will look at an atmospheric projection (projection of a media on the walls and roof around the patient) while receiving their planned care procedures. Researchers will compare an active group watching a video with a control group watching a simple colored light to see if the visualisation of an atmospheric projected video reduces pain and anxiety more than the visualisation of a colored light does.

Enrollment

62 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥18 ;
  • Patient requiring one of the following treatment procedures : suturing, plaster cast placement and/or repositioning, fracture or dislocation reduction, ascites puncture, pleural puncture, lumbar puncture.

Exclusion criteria

  • Patient clinically unstable;
  • Patient incapable of discernment or consent ;
  • Altered mental status (cognitive disorders, mental retardation, acute state of confusion, acute psychosis);
  • Alcoholic patient with University of California, San Diego Brief Assessment of Capacity to Consent (UBACC) score of 10/10 ;
  • Patient hard of hearing ;
  • Patient with visual impairments preventing him/her from perceiving his/her environment ;
  • Patient unable to understand the use of visual analog scales (VAS);
  • Impaired sensitivity of the part of the body where the medical intervention is to take place;
  • Planned use of analgesia/sedation with a dissociative agent (midazolam, ketamine, propofol);
  • Incarcerated patient ;
  • Patient transferred from another hospital ;
  • Patient having already participated in this study during a previous consultation in the emergency department of the Centre Hospitalier Universitaire Vaudois.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

62 participants in 2 patient groups

Atmospheric 3D video projection
Experimental group
Description:
Patients in the interventional arm will watch an immersive atmospheric video projection on the walls of their examination room.
Treatment:
Device: Immersive atmospheric projection
Atmospheric 3D color projection
Sham Comparator group
Description:
Patients in the interventional arm will look at a neutral color of their choice projected on the walls of their examination room.
Treatment:
Device: Minimal atmospheric projection

Trial contacts and locations

1

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Central trial contact

Pr. Chantal Berna Renella, MD PHD; Pr. Olivier Hugli, MPH

Data sourced from clinicaltrials.gov

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