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New stress program aims to help young women cope

NCT ID NCT07357129

Symptom relief Sponsor: Bogazici University Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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)
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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
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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This status has not been confirmed recently, so it may be out of date.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 pilot study will test a low-intensity program called Self-Help Plus (SH+) to help young women aged 18-29 manage stress. The program, developed by the World Health Organization, has been effective in other groups and will be used for the first time with Turkish-speaking women in Türkiye. Sixty participants with high stress levels will either receive the program immediately or after a 3-month wait, and researchers will measure changes in distress and depression symptoms.

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 60 people

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

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Sep 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 29 years

Sex

Female participants only

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: 1. being a woman 2. being ages between 18 and 29 3. being fluent in Turkish 4. having high levels of psychological distress (scoring above 15 on the Turkish version of the Kessler Psychological Distress Scale (K-10) Exclusion Criteria: 1. having an imminent risk of suicide (measured by WHO PM+ assessment tool) 2. having a diagnosis for severe mental disorder (e.g., psychotic disorders or substance dependence) 3. having cognitive impairment (e.g., received a diagnosis of dementia or severe intellectual disability) 4. currently receiving psychological treatment, e.g., therapy.

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As listed by the trial registrant

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

Stress (psychology)

How to take part

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  1. The official record

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    Open the record ↗

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