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