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New app aims to ease grief and prevent suicide after losing a baby

NCT ID NCT07011940

Symptom relief Sponsor: Oregon Research Behavioral Intervention Strategies, Inc. 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 16, 2026 · Updated 3 times

Summary

This study tests a mobile app called Along With Me to see if it can reduce post-traumatic stress and suicidal thoughts in parents who have recently lost a pregnancy or infant. About 300 participants will either use the app, use the app with support from a peer guide, or receive standard care. The goal is to find better ways to support grieving parents.

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 300 people

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

Started

Jul 2025

Expected to finish

Aug 2027

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

15 years and older

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: * Within the first month of pregnancy or early infant loss * Reside in the United State * Speak and read either English or Spanish at a 6th grade reading level * 15 or older Exclusion Criteria: * Not pregnant or has not experienced an early infant loss * Does not reside in the United State * Does not speak and read either English or Spanish at a 6th grade reading level * 14 or younger

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Conditions

The condition(s) this trial relates to.

Abortion, Spontaneous Infant Death post-traumatic stress disorder pregnancy disorder with abortive outcome Stillbirth sudden unexpected infant death Suicidal Ideation

As listed by the trial registrant

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

Grief Infant death Miscarriage Post-traumatic stress disorder Stillbirth Suicidal ideation

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. 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

  • Oregon Research Behavioral Intervention Strategies, Inc.

    RECRUITING

    Eugene, Oregon, 97477, United States

  • Oregon Research Behavioral Strategies, Inc.

    NOT_YET_RECRUITING

    Springfield, Oregon, 97477, United States

More trials for these conditions

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