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Brain training boosts Well-Being in traumatized new moms

NCT ID NCT06054412

Symptom relief Sponsor: Wayne State University 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 20, 2026 · Updated 2 times

Summary

This study looks at whether a brain-training technique called neurofeedback can help new mothers who have experienced trauma feel better and manage their emotions. Twenty postpartum women with trauma-related symptoms will try the training alongside their usual care. The goal is to see if it improves their well-being, reduces stress, and helps with parenting.

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 20 people

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

Started

Mar 2024

Expected to finish

Dec 2027

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

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: * Must have clinically concerning symptoms of Post-traumatic Stress Disorder and/or it's dissociative sub-type, as indicated by either a score of 3+ on the Primary Care PTSD Screen for DSM-5 (PC-PTSD-5) screening measure for PTSD symptoms OR endorsement of 2 or more past-month symptoms of moderate or greater severity on the depersonalization/derealization subscale of the Dissociative Subtype of PTSD Scale (DSPS). * Must be between 3-24 months postpartum * Must be receiving regular, primarily in-person psychotherapy from a therapist at a clinic in the Greater Detroit area. Exclusion Criteria: * Are currently pregnant * Have a lifetime history of significant untreated mental illness (not currently treated schizophrenia, schizoaffective disorder, bipolar disorder, or substance use disorder) or neurological or pervasive developmental disorder * Have a documented history of epilepsy * Have ever experienced previous head injury with loss of consciousness * Are currently experiencing domestic or intimate partner violence or otherwise state that their current living conditions are unsafe * Are currently experiencing psychosis or have been suicidal within the last six months * Are currently taking, or in the past month has taken benzodiazepines, narcotic drugs, or cannabis * Have engaged in self-harming behaviors in the last 3 months requiring medical attention * Do not have competence to understand or consent to the study procedures * Do not have fluency in written and spoken English

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Conditions

The condition(s) this trial relates to.

dissociative disorder Emotional Regulation mood disorder post-traumatic stress disorder Psychological Well-Being

As listed by the trial registrant

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

Dissociation Emotional regulation Maternal behavior Maternal care patterns Maternal distress Mood disturbance Post traumatic stress disorder Well-being, psychological

Contacts and locations

Locations

  • Wayne State University

    Detroit, Michigan, 48202, United States

More trials for these conditions

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