← Back to Clinical Trials
Recruiting NCT07649733

NCT07649733 Projecte Benestar 2026: Virtual Reality Program for Healthcare Workers

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07649733
Status Recruiting
Phase
Sponsor Badalona Serveis Assistencials
Condition Burnout, Healthcare Workers
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2026-06-08
Primary Completion 2027-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Projecte Benestar Virtual Reality Educational Program

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2026-06-08 with a primary completion date of 2027-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Projecte Benestar 2026 is a multicenter randomized controlled study evaluating a brief immersive educational program delivered through virtual reality for healthcare workers. The program is designed to support emotional well-being, self-care, mindfulness, and emotional regulation in professionals working in healthcare settings. Participants will be active healthcare or healthcare-support workers from participating centers. They will be randomly assigned to one of two groups. One group will receive the virtual reality program at the beginning of the study, while the other group will continue usual activity and receive the same program later, after a wait-list period. The main objective is to evaluate whether the program reduces emotional exhaustion, measured with the Maslach Burnout Inventory. Secondary objectives include evaluating changes in depersonalization, personal accomplishment, work engagement, usability, satisfaction, adherence, and tolerability of the virtual reality program.

Eligibility 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

Contact & Investigator

Central Contact

José Ferrer Costa, MD, MSc

✉ jfcosta@bsa.cat

📞 +34937407482

Principal Investigator

Jose Ferrer Costa, MD, MSc

PRINCIPAL INVESTIGATOR

Badalona Serveis Assistencials - Universitat Oberta de Catalunya

Frequently Asked Questions

Who can join the NCT07649733 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Burnout, Healthcare Workers. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07649733 currently recruiting?

Yes, NCT07649733 is actively recruiting participants. Contact the research team at jfcosta@bsa.cat for enrollment information.

Where is the NCT07649733 trial being conducted?

This trial is being conducted at Badalona, Spain, Valls, Spain.

Who is sponsoring the NCT07649733 clinical trial?

NCT07649733 is sponsored by Badalona Serveis Assistencials. The principal investigator is Jose Ferrer Costa, MD, MSc at Badalona Serveis Assistencials - Universitat Oberta de Catalunya. The trial plans to enroll 100 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology