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Not Yet Recruiting NCT07747766

Program for Alleviating Relationship Trauma and Stress for Intimate Partner Violence - Randomized Control Trial

Conditions: Individuals Who Use Violence, Interpersonal Violence

Sex: Male
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 48
Sponsor: Cambridge Health Alliance

Location: Cambridge Health Alliance Center for Mindfulness and Compassion Malden Massachusetts

Summary

This research study investigates the feasibility of a randomized control trial of a group-based treatment program for reducing stress, trauma, substance use, and use of violence among individuals who were court-mandated to attend a program after committing an act(s) of domestic violence. The study is in a 2-arm design with an intervention group and a control group.

Eligibility Criteria

Inclusion Criteria: * Must be male-identifying or prefer to be in a male-identifying group; * Must be a resident of Washington state; * Must be court-referred to a treatment program for using violence with an intimate partner; * Have sufficient English fluency and literacy skills to understand the consent process, procedures and questionnaires and have the ability to provide written informed consent; * Have access to the internet and an electronic device with adequate data capacity; to complete questionnaires online and attend online video conference groups; * Must be available and willing to attend at least 17 out of 20 scheduled online group sessions; and * Must be available and willing to complete the online computerized assessments, and phone interviews. Exclusion Criteria: * Insufficiently stable housing or internet connection to be able to join at least 17 group sessions; * Current participation in another experimental research study; * Expected medical hospitalization in the next six months from study enrollment period; * Current or expected physical incarceration (excluding house arrest or other forms of electronic monitoring) in the next six months from study enrollment period; * Inpatient hospitalization for mental health, substance use, suicide attempt or self-harm within past three months; * Inability to participate safely in the study intervention and without disrupting the group (in the opinion of principal investigator OR meeting any of the following criteria) * Past year history of a psychotic disorder or clinician confirmed active psychosis assessed by the Structured Clinical Interview for DSM-5 (SCID-5); * Bipolar I disorder history or current severe level of mania assessed by the Structured Clinical Interview for DSM-5 (SCID-5); * Acute suicidality with intent will be excluded from the study (Structured Clinical Interview for DSM-5 \[SCID-5\]); * High levels of Psychopathy as defined by self-report psychopathy checklist (SRP-4); * Self-injurious behavior in past three months will require clinical assessment prior to participation in the program; * Acute homicidality with plan and/or intent; * Inability to join a group without intoxication. * Prior experience or exposure with Internal Family Systems (e.g. IFS therapy, IFS groups or retreats, current IFS practice, etc.)

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07747766). StuddyBuddy aggregates publicly available trial information.