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The BEAR Therapeutic Program for Women

The Building Empowerment and Resilience Therapeutic Program for Women With a History of Trauma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04418778
Enrollment
120
Registered
2020-06-05
Start date
2023-03-01
Completion date
2026-07-31
Last updated
2025-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Anxiety, PTSD, Trauma, Psychological

Keywords

empowerment, therapeutic intervention

Brief summary

The current study aims to test a novel therapeutic intervention for women who have a history of interpersonal trauma. The Building Empowerment and Resilience (BEAR) Therapeutic group incorporates psychological skills, psychoeducation, and physical empowerment training, all within a therapeutic process. It will be implemented iwith women who have experienced interpersonal trauma (physical, sexual, or emotional abuse/neglect). The investigators aim to understand how this program effects one's self-efficacy and whether the program can reduce rates mental health problems (such as depression and anxiety) and reduce the rates of revictimization. Women who participate in the BEAR group must be able to attend in-person sessions. The control group can be remote.

Interventions

BEHAVIORALBEAR

Building Empowerment and Resilience Therapy group

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Women ages 18-70 2. History of physical, sexual, and/or emotional abuse/neglect/violence, with subsequent interpersonal or psychological distress (e.g., depression or anxiety) related to this history.

Exclusion criteria

1. Active, significant substance abuse 2. Significant medical conditions that would preclude safe participation in the study 3. High levels of depression with significant suicide risk 4. Psychiatric instability 5. History of assaultive behavior or is judged to be at potential risk to assault others.

Design outcomes

Primary

MeasureTime frameDescription
Trauma Symptom Inventory-II (TSI-2).baseline to post-group (3 months)The TSI-2 is a self-report measure of trauma-related symptoms and behaviors.
Change in Coping Self-Efficacy Scale (CSES)baseline to post-group (3 months)The CSES is designed to measure an individual's perception of her competence to carry out coping strategies effectively when faced with a challenge or threat.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026