Evaluating Healthcare Professionals' Satisfaction and Stress Mitigation Using Virtual Reality Intervention in Surgical Ward

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAmsterdam UMC, location VUmc

About this trial

The goal of this feasibility study is to learn whether a VR intervention is feasible, acceptable, and satisfactory for healthcare workers in surgical wards to help mitigate stress. Secondary objectives include assessing its potential contribution to stress reduction, user comfort, and practical integration into daily workflows.

Participants will take part in a single 10-minute VR intervention session.

Eligibility criteria

Qualifiers

Volunteering healthcare professionals (≥18 years old) working in direct patient care, such as nurses, residents, physician assistants, and surgeons, on the surgical ward.

Disqualifiers

Diagnosed with epilepsy

Experienced VR as a trigger for their migraines

Severe dizziness, nausea or physical disabilities will be excluded.

Diagnosed with arrythmias, bradycardia or tachycardia

Trial design

Treatments tested in this trial

  • Virtual Reality intervention

Treatment groups

75 Participants
are divided into 1 treatment group

Sponsors and collaborators

Amsterdam UMC, location VUmc

Lead sponsor

European Union (Horizon Europe Programme)

Collaborator

Rigshospitalet, Denmark

Collaborator

Universitätsklinikum Hamburg-Eppendorf

Collaborator