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Could a weekly group session boost resilience in mothers facing unique challenges?

NCT ID NCT07738289

Symptom relief Sponsor: Sinop 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 31, 2026 · Last updated Jul 31, 2026

Summary

This study tests whether a structured group therapy program can improve psychological resilience and family functioning in mothers who care for children with intellectual disabilities. Twenty mothers are randomly assigned to either the therapy group or a control group. The therapy involves seven weekly sessions led by a social worker, combining education, cognitive-behavioral techniques, mindfulness, and relaxation. Researchers measure resilience and family functioning before, right after, and three months later, and also gather personal stories to understand the experience.

What this could mean

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

Active substance
Structured group therapy (behavioral intervention)
What this could lead to
If effective, this group therapy could offer a practical, low-cost way to support mothers' mental health and strengthen family dynamics.
What could go wrong
This is a very small trial (20 participants) and early-stage, so results may not apply broadly. The therapy requires time and commitment, and benefits may vary.

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

20 people

The number who actually took part.

Started

Dec 2023

Finished

May 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

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 * Female adults aged 18 years or older. * Mothers who were the primary caregivers of a child diagnosed with intellectual disability according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria. * Had provided continuous care for the child with intellectual disability for at least five years. * Able to communicate in Turkish and participate in group sessions. * Voluntarily agreed to participate in the study and provided written informed consent. Exclusion Criteria * Presence of a chronic physical or mental illness severe enough to interfere with participation in the group intervention or group interaction. * Inability or unwillingness to participate throughout the intervention. * Withdrawal of informed consent at any stage of the study.

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Conditions

The condition(s) this trial relates to.

intellectual disability

As listed by the trial registrant

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

Family functioning Psychological resilience

Contacts and locations

Locations

  • Sinop University

    Sinop, Merkez, 57100, Turkey (Türkiye)

More trials for these conditions

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