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Preventing Mental Disorders Among Women Internally Displaced by War in Ukraine: The SHAWL Trial

Boston Medical Center (BMC) logo

Boston Medical Center (BMC)

Status

Completed

Conditions

War-Related Trauma
Prevention
Refugee Health
Mental Health Disorder
Depressive Symptoms Mild to Moderate in Severity
Acceptance and Commitment Therapy
Anxiety

Treatments

Behavioral: Attention control
Behavioral: Acceptance and Commitment Therapy

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06679114
H-45281
R34MH134077 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This study is a randomized controlled trial among 120 recently displaced women to determine the effectiveness of a single-session Acceptance and Commitment Therapy (ACT) group therapy on prevention of development of mental health disorders or worsened mental health symptoms.

Full description

The war in Ukraine has provoked the world's current largest humanitarian displacement: since February 2022, one-third of Ukrainians have been forced to leave their homes, resulting in upwards of 7 million internally displaced persons. Estimates suggest that 60% of Ukraine's displaced persons are women, who face stressors including difficulty accessing necessary primary health and psychological care, restricted access to food and stable housing, and increased strain from separation from their social networks and additional family care responsibilities.

Early reports from Ukraine consistently describe the psychological distress that displaced women are presently experiencing. It is anticipated that nearly one in five people exposed to conflict will develop mental disorders, notably depressive and anxiety disorders. Thus, improving access to mental health prevention programs that mitigate development of mental disorders for women in Ukraine is critical.

This study will adapt a community-based Acceptance and Commitment Therapy (ACT) intervention to prevent the development symptoms of depression and anxiety among women displaced by war in Ukraine. ACT is an evidence-based approach that uses acceptance, mindfulness and behavioral change processes to improve psychological flexibility. Recently displaced women who screen positive for symptoms of depression and anxiety will be recruited. The investigators plan to adapt and evaluate a single-session ACT group intervention to limit effects of mental health distress among these displaced women.

The central hypothesis of this research is that an ACT-based intervention delivered in a humanitarian context will help displaced women in Ukraine learn skills to improve psychological flexibility, thereby decreasing symptoms of depression and anxiety and ultimately mitigating onset of mental disorders.

Enrollment

120 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 or over
  • Identify as a displaced woman within one year of migration
  • Endorsing mild to moderate depressive symptoms (subscale score between 3 and 7) and/or anxiety symptoms (subscale score between 2 and 6) on the Mental Health Assessment Inventory (MHAI) but not exceeding the maximum score for either subscale (i.e., not exceeding 7 on the depressive symptoms subscale and not exceeding 6 on the anxiety symptoms subscale)
  • Ability to provide informed consent
  • Speak Ukrainian or Russian

Exclusion criteria

  • Diagnosis of a depressive or anxiety disorder, or symptoms necessitating urgent referral for evaluation of suicidal or homicidal ideation
  • Receipt of psychiatric care for depression or anxiety in the past 5 years
  • A severe medical problem that inhibits ability to participate in the trial

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 2 patient groups

Behavioral: ACT Therapy
Experimental group
Description:
Participants randomized to this group will receive a single-session ACT intervention
Treatment:
Behavioral: Acceptance and Commitment Therapy
Attention control
Active Comparator group
Description:
Participants in the control group will receive minimally enhanced usual care to receive treatment as usual enhanced by a health information group session.
Treatment:
Behavioral: Attention control

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Kimberly Hook, PhD, MA; Karsten Lunze, MD DrPH MPH

Data sourced from clinicaltrials.gov

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