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Can a training program turn trauma into growth for emergency nurses?

NCT ID NCT07677527

Symptom relief Sponsor: Fatima Jinnah Women University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 30, 2026 · Last updated Jul 08, 2026 · Updated 3 times

Summary

This study tests a structured program designed to help emergency nurses cope with the psychological impact of repeatedly witnessing traumatic events. The program combines education, mindfulness, and peer support to reduce distress and promote positive growth. Sixty nurses from emergency departments will be randomly assigned to either the program or a control group, with changes in their well-being measured over time.

What this could mean

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

Active substance
Psychoeducational Vicarious Post-Traumatic Growth Intervention
What this could lead to
If effective, this program could provide a practical way to support mental health and resilience in nurses regularly exposed to trauma.
What could go wrong
This is a small, early-stage trial with 60 participants, so results may not apply broadly. The intervention may not produce lasting benefits.

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 60 people

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

Started

Mar 2026

Expected to finish

Sep 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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: 1. Registered nurses currently employed in emergency departments. 2. Minimum six months of emergency department work experience. 3. Able to read and understand English or Urdu. 4. Willing to provide informed consent. 5. Available to participate throughout intervention and follow-up assessments. Exclusion Criteria: 1. Current diagnosis of severe psychiatric disorder requiring intensive treatment. 2. Current participation in trauma-focused psychotherapy. 3. Cognitive impairment affecting study participation. 4. Planned transfer from emergency unit during study period. 5. Refusal to provide informed consent.

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Conditions

The condition(s) this trial relates to.

Compassion Fatigue Psychological Well-Being

As listed by the trial registrant

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

Post-traumatic growth, psychological Psychological distress Psychological well-being Psychological well-being in emergency unit nurses Vicarious trauma

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

  • Nishtar Hospital, Burn Unit (NMH), Multan Institute of Cardiology (MIC), Bakhtawar Amin Hospital, Multan, Khawaja Fareed Social Security Hospital

    RECRUITING

    Multan, 59070, Pakistan

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