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Search / Trial NCT06888297

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Second Victim Phenomenon Healthcare Professionals Occupational Stress Peer Support Programs Psychological Support In Healthcare Patient Safety Healthcare Workforce Well Being Certification Of Support Interventions

ClinConnect Summary

The RESCUE trial is focused on helping healthcare professionals who experience the "second victim" phenomenon, which refers to the emotional distress they can face after being involved in stressful or traumatic events at work. This study aims to create and validate certification systems for support programs that help these professionals cope better and promote their well-being. By developing standards and training programs for peer supporters, the goal is to improve the overall support network within healthcare settings across Europe, ultimately enhancing patient safety and the quality of care.

To be eligible for the trial, participants must be healthcare professionals like doctors, nurses, or clinical managers with at least five years of experience in their field. They should currently work in a healthcare setting and be willing to take part in training and support activities related to the project. While the trial is not yet recruiting participants, those who do join can expect to engage in various training and evaluation processes aimed at improving support for themselves and their colleagues. This initiative is a significant step towards creating a healthier work environment for healthcare providers, which is vital for both their well-being and the safety of their patients.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Healthcare professionals (e.g., physicians, nurses, midwives, clinical managers, patient safety officers).
  • A minimum of 5 years of experience in healthcare-related fields such as clinical management, patient safety, quality assurance, or second victim support interventions.
  • Employed in a healthcare institution or involved in second victim support initiatives at the time of the study.
  • Willing to participate in peer support training, intervention certification, or evaluation processes related to the RESCUE project.
  • Able to provide informed consent to participate in the study.
  • Exclusion Criteria:
  • Non-healthcare professionals or individuals without experience in patient safety, clinical management, or second victim support.
  • Less than 5 years of professional experience in relevant fields.
  • Not affiliated with a healthcare institution or not involved in second victim support activities.
  • Unable to provide informed consent.

About Fundación Para El Fomento De La Investigación Sanitaria Y Biomédica De La Comunitat Valenciana

The Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana is a prominent clinical trial sponsor dedicated to advancing health research in the Valencian Community. By fostering collaboration between healthcare institutions, academic entities, and industry partners, the foundation aims to enhance biomedical innovation and improve public health outcomes. With a focus on prioritizing patient welfare and ethical research practices, it actively supports the development of cutting-edge therapies and medical solutions through rigorous clinical trials and research initiatives.

Locations

San Juan, Alicante, Spain

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported