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Behavioral Intervention
PARTS-NB for Domestic Violence (PARTS-IPV Trial)
Malden, MA
N/A
Recruiting
Led By Zev Schuman-Olivier, MD
Research Sponsored by Cambridge Health Alliance
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Must be male-identifying or prefer to be in a male-identifying group
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at 12 and 20 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial is looking at whether a group treatment program can help people who have been ordered by the court to attend a program after committing domestic violence. The program aims to reduce stress, trauma, substance use
See full description
Who is the study for?
This trial is for male-identifying individuals in Washington state, court-mandated to attend a program after domestic violence incidents. Participants must have internet access, be willing to attend most online sessions and complete assessments. Exclusions include severe mental health issues like bipolar I disorder or acute suicidality, unstable housing, concurrent experimental studies participation, recent hospitalizations, high psychopathy levels or severe personality disorders.Check my eligibility
What is being tested?
The PARTS-NB program is being tested for its effectiveness in reducing stress, trauma, substance use and violent behavior among men mandated to receive treatment for domestic violence. The study involves attending online group sessions and completing questionnaires to assess the impact of the intervention.See study design
What are the potential side effects?
As this trial involves a behavioral intervention rather than medication, traditional side effects are not applicable. However, participants may experience emotional discomfort or distress when discussing traumatic experiences or confronting their behaviors during therapy.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I identify as male or prefer male group settings.
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Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at 12 and 20 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at 12 and 20 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Feasibility of Intervention
Secondary study objectives
Acceptability of Intervention
Intervention Satisfaction
Revised Conflict Tactics Scale (CTS2)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: PARTS-NBExperimental Treatment1 Intervention
All study participants will be in the PARTS-NB arm and go through the treatment program called "Program for Alleviating Relationship Trauma and Stress through New Behaviors".
Find a Location
Closest Location:Cambridge Health Alliance Center for Mindfulness and Compassion· Malden, MA· 644 miles
Who is running the clinical trial?
Cambridge Health AllianceLead Sponsor
63 Previous Clinical Trials
22,330 Total Patients Enrolled
Boston UniversityOTHER
493 Previous Clinical Trials
9,998,028 Total Patients Enrolled
Washington State Department of Social and Health ServicesOTHER
3 Previous Clinical Trials
299 Total Patients Enrolled
Washington State Department of Commerce Office of Crime Victims AdvocacyUNKNOWN
Zev Schuman-Olivier, MDPrincipal InvestigatorCambridge Health Alliance Center for Mindfulness and Compassion
16 Previous Clinical Trials
2,193 Total Patients Enrolled