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Can a simple care plan reduce stress for trauma survivors in the hospital?

NCT ID NCT06330753

Symptom relief Sponsor: Brigham and Women's Hospital 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
Registered, but not yet taking participants.
By invitation only This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a trauma-informed care plan (TICP) placed in the electronic medical record helps healthcare teams better care for patients with trauma and complex needs. About 200 patients and their clinicians will use the plan, and researchers will measure how acceptable, appropriate, and feasible it is. The goal is to see if the plan improves patient satisfaction and reduces anxiety during healthcare visits.

What this could mean

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

Active substance
Trauma-informed care plan (a written plan placed in the electronic medical record to guide healthcare team interactions)
What this could lead to
If it works, this could help healthcare teams better understand and support patients with trauma, reducing patient stress and improving care satisfaction.
What could go wrong
This is a small, early-stage study focused on feasibility and acceptability, not on proving health outcomes. The plan may not change actual care or may not work in other settings.

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 200 people

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

Started

Jan 2025

Expected to finish

Nov 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

18 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: * patients ( ages 18-60) * who have frequent health care appointments * have complex health care needs * consent to participate in study * English or spanish speaking. Exclusion Criteria: * patients less than 18 and older than 60. * patients too ill (medically/phytologically) to consent. * suicidal or homicidal patients.

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Conditions

The condition(s) this trial relates to.

acute stress disorder Coitus injury

As listed by the trial registrant

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

Trauma and stressor related disorders Violence, domestic Violence, sexual Violence, structural

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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    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

  • Brigham and Women's Hospital

    Boston, Massachusetts, 02116, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.