Design of an Intervention to Equip Middle Managers and Managers in Healthcare Institutions with Tools to Increase the Resilience of Their Teams (e-Resiliencia)

December 4, 2024 updated by: Irene Carrillo Murcia

Diseño De Una Intervención Para Dotar a Mandos Intermedios Y Directivos De Instituciones Sanitarias Con Herramientas Para Incrementar La Resiliencia De Sus Equipos

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Spain
    • Alicante
      • Elche, Alicante, Spain, 03202
        • Universidad Miguel Hernandez de Elche

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Healthcare professionals and middle management in active healthcare institutions.

Exclusion Criteria:

  • Inability to complete the web-based intervention due to access difficulties or lack of digital literacy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: e-Resilience Intervention
Middle management and healthcare professionals who voluntarily participate in the e-Resilience intervention.
Other: Resilience training intervention
Training intervention on tools and strategies to strengthen the resilience of work teams in healthcare centres.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of incorporations and adaptations necessary for the validation of e-Resilience in a relevant environment.
Time Frame: 5 months
Number of change proposals of the expert group to adapt the tool to the target environments' needs and enhance its applicability.
5 months
Hits on resilience knowledge questionnaire (pre-intervention).
Time Frame: 3 months
Number of correct answers to questions on knowledge of models, techniques, tools and strategies for building resilience in clinical settings.
3 months
Hits on resilience knowledge questionnaire (post-intervention).
Time Frame: 3 months
Number of correct answers to questions on knowledge of models, techniques, tools and strategies for building resilience in clinical settings.
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clarity of the e-Resilience tool components.
Time Frame: 3 months
Clarity of the e-Resilience tool components (scale 1-5, where 1 = not clear at all and 5 = totally clear).
3 months
Usefulness and applicability of the e-Resilience tool.
Time Frame: 3 months
Usefulness and applicability of the e-Resilience tool (scale 1-5, where 1 = not useful or applicable at all and 5 = fully useful and applicable).
3 months
Perception of improvement of own capacity to strengthen the resilience of healthcare teams.
Time Frame: 3 months
The contents of the course have allowed me to learn strategies to strengthen the resilience of the professionals or teams in my charge (scale 1-5, where 1 = strongly disagree and 5 = strongly agree).
3 months
Willingness to recommend e-Resilience.
Time Frame: 3 months
I will recommend the intervention to other colleagues (scale 1-5, where 1 = strongly disagree and 5 = strongly agree).
3 months
Willingness to use e-Resilience in the future.
Time Frame: 3 months
I will apply any of the tools or strategies learned to strengthen individual, team or organisational resilience in my work environment. (scale 1-5, where 1 = strongly disagree and 5 = strongly agree).
3 months
Overall satisfaction with the e-Resilience intervention.
Time Frame: 3 months
Overall satisfaction with the e-Resilience intervention (scale 0-10, where 0 = not at all satisfied and 10 = completely satisfied).
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Irene Carrillo Murcia

Collaborators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2024

Primary Completion (Actual)

November 26, 2024

Study Completion (Actual)

November 26, 2024

Study Registration Dates

First Submitted

November 29, 2024

First Submitted That Met QC Criteria

December 4, 2024

First Posted (Estimated)

December 9, 2024

Study Record Updates

Last Update Posted (Estimated)

December 9, 2024

Last Update Submitted That Met QC Criteria

December 4, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ILISABIO22_AP09

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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