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Design of an Intervention to Equip Middle Managers and Managers in Healthcare Institutions with Tools to Increase the Resilience of Their Teams

NCT06724770 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-12-09

No results posted yet for this study

Summary

The main objective of this preparatory action (experimental study without control group, before and after measurements) is to develop and test the feasibility of the e-Resilience tool in a relevant environment (TRL6). This web-based tool has been designed to facilitate the work of the top and middle management of healthcare institutions to strengthen the resilience of their teams to face critical situations inherent to healthcare activity.

The main questions it aims to answer are:

1. Which components of the e-Resilience intervention need to be improved?
2. Does the e-Resilience tool improve the knowledge of middle managers in healthcare institutions on specific techniques and strategies to strengthen the resilience of the professionals and teams under their care?
3. Is the e-Resilience tool helpful and applicable to clinical settings in the opinion of middle managers in healthcare institutions?

Participants in the study are middle management and healthcare professionals from primary care centres and hospitals in the Valencian Community (Spain). A group of experts review the components of the intervention/tool to improve its adaptability to clinical settings. Subsequently, a sample of healthcare professionals and middle managers complete the intervention by answering a knowledge questionnaire before and after the intervention and a survey to evaluate the tool.

There is no control group.

Conditions

  • Occupational Health
  • Resilience
  • Job Stress
  • Well-being At Work
  • Highly Stressful Situations
  • Healthcare Worker

Interventions

OTHER

Resilience training intervention

Training intervention on tools and strategies to strengthen the resilience of work teams in healthcare centres.

Sponsors & Collaborators

  • Foundation for the Promotion of Healthcare and Biomedical Research in the Valencian Community (FISABIO)

    collaborator UNKNOWN

  • Irene Carrillo Murcia

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
26 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-15
Primary Completion
2024-11-26
Completion
2024-11-26

Countries

  • Spain

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 NCT06724770 on ClinicalTrials.gov