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Can a Six-Week resilience programme sharpen emergency Nurses' skills and Well-Being?

NCT ID NCT07703319

Disease control Sponsor: Nablus University for Vocational and Technical Education Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 14, 2026 · Last updated Jul 17, 2026 · Updated 2 times

Summary

This study tests whether a six-week resilience-building programme can improve psychological well-being and advanced life support performance among emergency nurses in Palestinian hospitals. The programme includes cognitive-behavioural techniques, mindfulness, and stress management. Nurses in the intervention group will complete questionnaires and a simulated emergency scenario to measure changes. The goal is to see if building resilience helps nurses cope better and perform more effectively under pressure.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
a six-week culturally adapted resilience-building programme combining cognitive-behavioural techniques, mindfulness, stress inoculation training, and mental rehearsal
What this could lead to
If effective, this programme could offer a practical way to boost mental health and clinical skills in high-stress emergency nursing environments.
What could go wrong
This is a small, quasi-experimental study in one region, so results may not apply broadly. The intervention is behavioural and relies on self-report and simulation, which may not reflect real-world performance.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 140 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

23 to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Registered nurses currently employed in the Emergency Department of the selected Palestinian hospitals. Nurses working full-time Willingness to commit to the 6-week intervention program and complete all simulation-based assessments. Provided written informed consent to participate in the study. Exclusion Criteria: * Nurses who have participated in formal resilience or stress management training programs within the past year. Nurses currently receiving medical or psychological treatment for diagnosed mental health conditions. Nurses with physical or medical conditions that prohibit them from performing Advanced Life Support (ALS) chest compressions during the simulation assessment.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Resilience, psychological

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Saqr

    Nablus, West Bank, 00970, Palestinian Territories

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