NCT06724770

Brief 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. 1.Which components of the e-Resilience intervention need to be improved?
  2. 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. 3.Is the e-Resilience tool helpful and applicable to clinical settings in the opinion of middle managers in healthcare institutions?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 15, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 26, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 26, 2024

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

November 29, 2024

Completed
10 days until next milestone

First Posted

Study publicly available on registry

December 9, 2024

Completed
Last Updated

December 9, 2024

Status Verified

December 1, 2024

Enrollment Period

11 months

First QC Date

November 29, 2024

Last Update Submit

December 4, 2024

Conditions

Outcome Measures

Primary Outcomes (3)

  • Number of incorporations and adaptations necessary for the validation of e-Resilience in a relevant environment.

    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).

    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).

    Number of correct answers to questions on knowledge of models, techniques, tools and strategies for building resilience in clinical settings.

    3 months

Secondary Outcomes (6)

  • Clarity of the e-Resilience tool components.

    3 months

  • Usefulness and applicability of the e-Resilience tool.

    3 months

  • Perception of improvement of own capacity to strengthen the resilience of healthcare teams.

    3 months

  • Willingness to recommend e-Resilience.

    3 months

  • Willingness to use e-Resilience in the future.

    3 months

  • +1 more secondary outcomes

Study Arms (1)

e-Resilience Intervention

EXPERIMENTAL

Middle management and healthcare professionals who voluntarily participate in the e-Resilience intervention.

Other: Resilience training intervention

Interventions

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

e-Resilience Intervention

Eligibility Criteria

Age26 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Healthcare professionals and middle management in active healthcare institutions.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universidad Miguel Hernández de Elche

Elche, Alicante, 03202, Spain

Location

Related Publications (19)

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    PMID: 30653550BACKGROUND
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    PMID: 33998338BACKGROUND
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    PMID: 32905028BACKGROUND
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    PMID: 34766796BACKGROUND
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    PMID: 32940160BACKGROUND
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    PMID: 24064782BACKGROUND
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    PMID: 18696313BACKGROUND
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    PMID: 7850498BACKGROUND
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    PMID: 2723619BACKGROUND
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    PMID: 32306981BACKGROUND
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    PMID: 31744109BACKGROUND
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    PMID: 25384822BACKGROUND
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    PMID: 29870489BACKGROUND

Related Links

MeSH Terms

Conditions

Occupational Stress

Condition Hierarchy (Ancestors)

Occupational DiseasesStress, PsychologicalBehavioral SymptomsBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: Participants voluntarily adhere to the intervention. The intervention consists of the review and use of the e-Resilience tool. It is a toolkit that provides training in skills to strengthen the resilience of teams working in healthcare institutions. Participants complete knowledge questionnaires before and after the intervention. There is no control group.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

November 29, 2024

First Posted

December 9, 2024

Study Start

January 15, 2024

Primary Completion

November 26, 2024

Study Completion

November 26, 2024

Last Updated

December 9, 2024

Record last verified: 2024-12

Locations