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Not yet recruitingNCT07902050BEAR-SIUpdated Oct 28, 2026

BEAR for Women Who Have Experienced Sexual Assault and Have Suicidal Thoughts

An interventional study of BEAR Therapeutic Group in Sexual Assault and Rape and Suicidal Thoughts, sponsored by Stanford University. Not yet recruiting at 1 site in United States. Open to female participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-10-28.

Sponsored by Stanford University · Not applicable, Interventional, and Treatment

Updated Oct 28, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
Female
01

Study summary

The goal of this clinical study is to learn if the BEAR intervention effects outcome in women who have experienced sexual assault (broadly defined) and who have suicidal thinking. The main questions it aims to answer are:

  • Does this intervention decrease suicidal ideation?
  • Can this intervention increase self-efficacy in this population?

All women will participate in a 12 week therapy group, which is conducted in-person.

Participants will

  • Actively participate in the intervention, which is 1.5 hours, once per week for 12 weeks.
  • Complete weekly forms prior to group about suicidal thoughts and behaviors
  • Complete a series of questionnaires at baseline, six weeks, post-group, and at 3- and 12- month follow up.
  • Complete a qualitative interview about their experience of the intervention at post-group and one year follow up.
Read the detailed description

The study seeks cisgender women who have experienced sexual assault, broadly defined, and who also have suicidal thoughts and behaviors. The Building Empowerment and Resilience (BEAR) intervention is a 12-week manualized group therapy program developed for women who have experienced interpersonal violence. The group meets for 12 weeks, 1.5 hours each week. Participants must attend in-person, and it will only be conducted in Palo Alto, CA. All participants will receive the BEAR program.

The BEAR program integrates three components: 1) psychoeducation, 2) psychological skills, and 3) physical self-defense training. The psychoeducation component of the class covers topics such as healthy and unhealthy relationships, understanding stress response reactions in trauma, and shame and guilt. Social and cultural expectations are also discussed and linked to interpersonal violence.

The second component of the program advances a variety of skills that are important in all facets of the women's lives. These include skills such as assertiveness training, which is how to effectively stand up for one's rights; communication skills, which is how to communicate effectively through both verbal and nonverbal (body) language; and coping skills, which is how to managing stress and suicidal thoughts.

Physical self-defense skills are the final component of the program. An aim of the physical empowerment is to help the women embody their physical strength and voice. This physical aspect includes learning to use various levels of their voice; physical resistance moves that offer maximal opportunity for impact on an aggressor while minimizing harm to the women; specific hand/leg techniques (e.g., punching, kicking); where to target if they were attacked (e.g., nose); and training in "escape" skills that address breaking out of holds that are used by potential perpetrators (e.g., wrist grab or bear hug).

Intended group sizes will be 8-10 women per group, ages 18-75. A screening interview will be conducted to ensure eligibility. Assessments will be completed at baseline, six weeks into the group, post-group, and three- and twelve- months follow up. At each assessment point, a series of questionnaires will be completed. Additionally, after completion of the group and at the 12-month follow-up, a qualitative interview about their experience of the intervention will be conducted.

02

Conditions studied

  • Sexual Assault and Rape
  • Suicidal Thoughts

Keywords

  • sexual assault
  • suicidal thinking
  • depression
  • PTSD
  • anxiety
03

In context

Suicidal Ideation

569 studies on the registry are indexed under Suicidal Ideation; 203 are open to participants now.

This study's planned enrollment of 36 is below the median of 80 across 469 interventional studies indexed under Suicidal Ideation.

Browse Suicidal Ideation studies →

Lead sponsor

Stanford University is the lead sponsor of 2,168 studies on the registry; 431 are open to participants now.

Of its 267 completed or terminated interventional studies of FDA-regulated products, 207 (78%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Women ages 18-75
  2. History of sexual assault broadly defined with interpersonal or psychological distress (e.g., depression or anxiety) related to this history.
  3. Suicidal ideation or behaviors

Exclusion criteria

Exclusion Criteria:

  1. Active, significant substance abuse, which would interfere with participation
  2. Significant medical conditions that would preclude safe participation in the study
  3. No history of sexual assault
  4. Psychiatric instability
  5. History of assaultive behavior or is judged to be at potential risk to assault others.
  6. No current suicidal ideation or behaviors
  7. People who are unable to commit to the group for 12 weeks
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    BEAR therapy group

    The BEAR program integrates three components in a therapy group: psychoeducation (e.g., healthy relationships, stress response system, gender roles and socialization), psychological skills (e.g., assertive communication, coping skills, mindfulness), and physical self-defense (e.g., use of voice, physical techniques to maintain safety) training. (see detailed description).

    Behavioral: BEAR Therapeutic Group

Interventions

  • BehavioralBEAR Therapeutic Group

    The BEAR program is a 12-week manualized group therapy program developed for women who have experienced sexual assault and have suicidal thinking. The program integrates three components: psychoeducation (e.g., healthy relationships, stress response system, gender roles and socialization), psychological skills (e.g., assertive communication, coping skills, mindfulness), and physical self-defense training (e.g., use of voice, physical techniques to maintain safety). The therapeutic group meets for 12 weeks, 1.5 hours each week. This is an in-person study and participants must attend in-person. The program will be conducted in Palo Alto, CA only.

06

What researchers measure

Primary outcomes

  1. Change in suicidal thinking from baseline to immediately post-treatment as measured by the Beck Scale for Suicidal Ideation

    Beck Scale for Suicide Ideation (BSSI) is a 21-item instrument used to measure the severity of suicidal ideation in adults. The severity of suicidal ideation is calculated by summing the ratings for the first 19 items, and total BSS scores can range from 0 to 38 points, with higher numbers indicating more severe suicidal ideation.

    Time frame: From baseline to end of treatment at 12 weeks

  2. Change in baseline coping self-efficacy to immediately post-treatment on the coping self-efficacy scale

    The Coping Self-efficacy Scale is used to measure coping self-efficacy. There are 26 items, rating on a scale with the following anchor points: 0 (cannot do at all), 5 (moderately certain can do), and 10 (certain can do). Total scale scores range from 0 to 260, with higher scores meaning high coping self-efficacy.

    Time frame: From baseline to end of treatment at 12 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 28, 2026
Show all 1 update
  1. Oct 28, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07902050
Collaborators
American Foundation for Suicide Prevention
Responsible party
Jennifer Keller (Clinical Professor, Stanford University) — Principal investigator
First posted
Oct 28, 2026
Start date
Dec 2026 (estimated)
Primary completion
Jan 2029 (estimated)
Completion
Jan 2030 (estimated)
Last update
Oct 28, 2026

Study contacts

Clinical Research Coordinator
Contact
bearstudy@stanford.edu
650-724-7184
Jennifer Keller, PhD
principal investigator · Stanford University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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