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Life sciences · Interventional Study
ClinicalTrials.gov · October 28, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07902050). This is a study registration, not published results. Lead sponsor: Stanford University. Recruitment status: NOT_YET_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 36 participants (ESTIMATED). Conditions: Sexual Assault and Rape, Suicidal Thoughts. Interventions: BEHAVIORAL: BEAR Therapeutic Group. Primary outcome measures: Change in suicidal thinking from baseline to immediately post-treatment as measured by the Beck Scale for Suicidal Ideation , From baseline to end of treatment at 12 weeks; Change in baseline coping self-efficacy to immediately post-treatment on the coping self-efficacy scale , From baseline to end of treatment at 12 weeks. Brief 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.