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

NCT07155681 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2025-09-04

No results posted yet for this study

Summary

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.

Conditions

  • Stress
  • Stress (Psychology)

Interventions

DEVICE

Virtual Reality intervention

Virtual Realtiy intervention with biofeedback for 10 minutes during a shift on the ward for healthcare professionals

Sponsors & Collaborators

  • European Union (Horizon Europe Programme)

    collaborator UNKNOWN

  • Rigshospitalet, Denmark

    collaborator OTHER

  • Universitätsklinikum Hamburg-Eppendorf

    collaborator OTHER

  • Amsterdam UMC, location VUmc

    lead OTHER

Principal Investigators

  • Anne Eskes, associate professor · AmsterdamUMC

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-11-01
Primary Completion
2026-04-01
Completion
2026-06-01

Countries

  • Denmark
  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07155681 on ClinicalTrials.gov