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Tiny tots, big healing: EMDR shows promise for preterm babies with trauma

NCT ID NCT07590778

Symptom relief Sponsor: Tanja Holtackers 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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested a storytelling version of EMDR therapy in 10 preterm-born infants (0-2 years old) who had post-traumatic stress symptoms from medical care. Parents reported daily on their child's symptoms, sleep, and emotional functioning. The goal was to see if this early intervention is feasible and can reduce trauma-related stress in these vulnerable babies.

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

10 people

The number who actually took part.

Started

Feb 2025

Finished

Feb 2026

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

0 to 24 months

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Preterm birth (\<37 weeks gestational age) * Age between 0 and 24 months * Presence of frequent and severe post-traumatic stress symptoms (occurring daily to multiple times per week), considered related to medical trauma following premature birth * Not currently hospitalized * Availability of a parent or legal guardian able to provide informed consent Exclusion Criteria: * Insufficient proficiency in Dutch to complete study procedures and questionnaires * Severe physical illness or medical condition that is considered to be the primary focus of clinical care and/or interferes with participation in the intervention * Current participation in other trauma-focused psychological treatment

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Conditions

The condition(s) this trial relates to.

Premature Birth

As listed by the trial registrant

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

Post-traumatic stress symptoms Preterm infant

Contacts and locations

Locations

  • St. Antonius Hospital

    Utrecht, Utrecht, Netherlands

More trials for these conditions

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