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New group therapy aims to ease trauma after childbirth

NCT ID NCT07246356

Symptom relief Sponsor: University of Birmingham 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a group therapy program (GTEP) can help reduce trauma symptoms in people who had a traumatic birthing experience. Ten participants will join online sessions and complete questionnaires about their symptoms and well-being. The goal is to see if this approach is feasible and helpful for improving mental health and parent-infant bonding.

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 10 people

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

Started

Jun 2025

Expected to finish

Jun 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 65 years

Sex

Female participants only

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: * Aged between 18-65 years. * Currently under the Black Country Perinatal Mental Health Service * Experiencing self-reported trauma symptoms related to a birthing experience within the last 18 months (this includes the birth itself, the postnatal hospital stay, and/or any neonatal admissions). * Access to technology (e.g., laptop, internet connection) to be able to access the online group. * Access to a confidential space within their home, and childcare for their baby/any other existing children. * Proficient levels of English Language to engage with the group. * Ability to engage in group therapy based on clinical presentation. * Capacity to consent to engage in the GTEP group and research study. Exclusion Criteria: * Women/birthing people whose baby is no longer under their care. * Severe and enduring mental health presentations (i.e., diagnosis of bipolar, psychosis and/or schizophrenia. * Significant sensory impairment (e.g., needing a British Sign Language interpreter).

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Conditions

The condition(s) this trial relates to.

Birth Injuries post-traumatic stress disorder

As listed by the trial registrant

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

Bonding Psychological wellbeing PTSD (childbirth-related)

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

  • Black Country Healthcare NHS Foundation Trust

    RECRUITING

    Wolverhampton, WV4 5HN, United Kingdom

More trials for these conditions

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