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Stress relief for refugee families: a new hope for mothers and kids

NCT ID NCT07062341

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study looks at whether a group stress management program called Self-Help Plus (SH+) can improve the mental health of refugee mothers and their preschool children in Uganda. About 725 mothers and their children will take part, with some villages getting the program and others getting usual care. The goal is to see if helping mothers cope with stress also helps their children thrive.

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

725 people

The number who actually took part.

Started

Oct 2025

Expected to finish

Feb 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 years and older

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 (Mothers): * Aged 18 years or older * Able to speak and understand Juba Arabic * Mother of a child aged 3-4 years at the time of enrollment * Not planning to move away from the study area (Rhino Camp) within the next year * At least moderate psychological distress, defined as a score ≥5 on the Kessler-6 (K6) screening scale Exclusion Criteria (Mothers): * Currently participating in another structured mental health intervention * Prior participation in SH+, or familiarity with its content * Imminent risk of suicide, assessed using the suicidality subscale of the Mini International Neuropsychiatric Interview (MINI) * Observable signs of psychosis, manic behavior, or intellectual disability that would preclude meaningful participation (as judged by trained assessors) Inclusion Criteria (Children): * Aged 3-4 years at the time of baseline enrollment * Resides with the enrolled mother in one of the selected villages in Rhino Camp * The child's mother meets all eligibility criteria and is enrolled in the trial * Provides assent Exclusion Criteria (Children): * Known cognitive impairment or developmental delay that would prevent participation in age-appropriate assessments, based on maternal report and enumerator judgment * Physical health condition that would prevent safe participation at the time of data collection

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Conditions

The condition(s) this trial relates to.

Psychological Well-Being

As listed by the trial registrant

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

Contacts and locations

Locations

  • Kabale University

    Kabale, Uganda

More trials for these conditions

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