Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

Virtual Reality Program to Support Healthcare Workers

Official title: Projecte Benestar 2026: Multicenter Study of the Effectiveness and Implementability of an Immersive Educational Program for Workers in Healthcare Settings

Run by Badalona Serveis Assistencials · NCT07649733 · Data updated 2026-11-12

A brief immersive virtual reality program is being tested to see if it helps reduce burnout and improve well-being for healthcare workers.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorBadalona Serveis Assistencials
Academic / other
Locations2 sites (Badalona, Barcelona and 1 other locations)
StatusRecruiting
StartedJune 8, 2026
Main results expectedDecember 2027
Study endsDecember 2027
Registry record updatedJune 16, 2026
Trial IDNCT07649733 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Active healthcare or healthcare-support staff at participating centers aged 18 or older who can consent and commit to weekly VR sessions and study questionnaires.

Probably not a fit

Individuals unable to use VR headsets due to photosensitive epilepsy, motion sickness, or visual/hearing impairments may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multicenter randomized controlled trial tests a VR-based educational program designed to support emotional well-being, self-care, mindfulness, and emotional regulation for healthcare workers. Participants are active staff at participating centers and are randomized to receive the VR program immediately or after a six-month wait-list period. The intervention comprises eight short VR sessions, each 9 to 15 minutes long, delivered via autonomous headsets. Primary outcome is emotional exhaustion measured by the Maslach Burnout Inventory; secondary outcomes include depersonalization, personal accomplishment, work engagement, usability, satisfaction, adherence, and tolerability. The design allows all participants to receive the program while enabling a comparison between immediate and delayed intervention groups.

Why it matters

Potential benefit: If successful, the program could reduce burnout and improve well-being among healthcare workers.

How similar studies have gone: Previous VR-based well-being initiatives in healthcare have shown potential, but this specific delayed-start, multicenter RCT is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Active permanent or temporary staff member at a participating healthcare center where the program is implemented
* Age 18 years or older
* Able to understand, accept, and sign the informed consent form
* Willing to complete the study procedures, attend the planned weekly sessions, and complete the study questionnaires

Exclusion Criteria:

* Photosensitive epilepsy or history of seizures triggered by visual stimuli
* Severe motion sickness or previous intolerance to immersive devices
* Visual or hearing impairment that prevents adequate use of the virtual reality headset

Where it's running

  • Badalona Serveis Assistencials
    Badalona, Barcelona, Spain
    Recruiting
  • ABS Valls Urbà | Gerència d'Atenció Primària i a la Comunitat
    Valls, Tarragona, Spain
    Recruiting

Study contacts

  • Principal investigator: Jose Ferrer Costa, MD, MSc — Badalona Serveis Assistencials - Universitat Oberta de Catalunya
  • Study coordinator: José Ferrer Costa, MD, MSc
  • Email: jfcosta@bsa.cat
  • Phone: +34937407482

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.