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Can a simple message help close the depression treatment gap?

NCT ID NCT05580406

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether sending outreach messages (via secure messaging or phone) to people from racial and ethnic minority groups could help them start depression treatment after a new diagnosis. The study included 309 adults who had not started treatment within 30 days of diagnosis. The goal was to see if this approach could reduce disparities in depression care.

What this could mean

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

Active substance
outreach messaging
What this could lead to
If successful, this approach could help reduce racial and ethnic disparities in depression treatment initiation.
What could go wrong
This is a small pilot study, so results may not apply broadly. The outreach method may not work for all groups or 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

309 people

The number who actually took part.

Started

Apr 2023

Finished

Dec 2024

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 years and older

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: * New diagnosis of major depressive disorder or dysthymic disorder at a primary care visit ("new" defined as no depression diagnosis, psychotherapy visit or filled antidepressant prescription in the prior year) * Continuously enrolled in the participating health system for 365 days prior to the eligible diagnosis (to assure capture of prior diagnoses or treatments) * Patients Health Questionnaire-9 (PHQ-9) depression score of 10 or more within 14 days before to 7 days after the eligible diagnosis * No filled prescription for any antidepressant medication OR psychotherapy visit attended within 30 days of the eligible diagnosis\* * No recorded PHQ-9 depression score less than 5 since the eligible diagnosis * At least 18 years of age or older Exclusion Criteria: * Diagnosis of schizophrenia or bipolar disorder in the prior 2 years * Not registered to use Electronic Health Record (EHR) patient portal * Previously requested to not be contacted for research

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Henry Ford Health

    Detroit, Michigan, 48202, United States

  • Kaiser Permanente, Hawaii Market

    Honolulu, Hawaii, 96817, United States

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