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Blended Facilitation for Domestic Violence

N/A
Waitlist Available
Led By Katherine M. Iverson, PhD MA BA
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up for each site, the proportion calculated in the latter half of the facilitation phase (months 7-9) will be compared to the proportion calculated for the last three months of the maintenance phase (months 19-21)
Awards & highlights

Study Summary

This trial will study the effects of a new program to screen women Veterans for intimate partner violence.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~for each site, the proportion calculated in the latter half of the facilitation phase (months 7-9) will be compared to the proportion calculated for the last three months of the maintenance phase (months 19-21)
This trial's timeline: 3 weeks for screening, Varies for treatment, and for each site, the proportion calculated in the latter half of the facilitation phase (months 7-9) will be compared to the proportion calculated for the last three months of the maintenance phase (months 19-21) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Disclosure Rate (primary clinical effectiveness outcome)
Change in Reach (primary implementation outcome)
Secondary outcome measures
Adoption of Screening (secondary implementation outcome)
Change in Adoption of Referrals / Resource Provision (secondary implementation outcome)
Change in Implementation Fidelity (secondary implementation outcome)
+2 more

Trial Design

2Treatment groups
Experimental Treatment
Group I: Toolkit + Implementation as UsualExperimental Treatment2 Interventions
Participating clinics assigned to this arm will receive a guiding toolkit and implementation as usual regarding IPV screening practices.
Group II: Toolkit + Blended FacilitationExperimental Treatment2 Interventions
Participating clinics assigned to this arm will receive a guiding toolkit and blended facilitation to support IPV screening practices.

Find a Location

Who is running the clinical trial?

VA Office of Research and DevelopmentLead Sponsor
1,609 Previous Clinical Trials
3,299,182 Total Patients Enrolled
VA Boston Healthcare SystemFED
68 Previous Clinical Trials
963,031 Total Patients Enrolled
Katherine M. Iverson, PhD MA BAPrincipal InvestigatorVA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
1 Previous Clinical Trials
60 Total Patients Enrolled

Media Library

Blended Facilitation Clinical Trial Eligibility Overview. Trial Name: NCT04106193 — N/A
Domestic Violence Research Study Groups: Toolkit + Implementation as Usual, Toolkit + Blended Facilitation
Domestic Violence Clinical Trial 2023: Blended Facilitation Highlights & Side Effects. Trial Name: NCT04106193 — N/A
Blended Facilitation 2023 Treatment Timeline for Medical Study. Trial Name: NCT04106193 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is participation in this medical study limited to individuals over 35 years of age?

"For admittance into this trial, participants must be between 18 and 100 years old. Alternatively, those under the age of 18 can take part in 2 clinical trials while 6 separate studies are available to individuals over 65."

Answered by AI

Is it still possible to enroll in this research endeavor?

"Contrary to expectations, clinicaltrials.gov states that this research is not currently recruiting patients even though it was initially posted on November 1st 2020 and updated lastly in November 3rd 2022. For those seeking treatment options, 10 other studies are presently enrolling subjects at the moment."

Answered by AI

How many places are administering this trial?

"Presently, 8 clinical sites are recruiting participants for the trial. The locations consist of Albuquerque's New mexico VA Health Care System, Sacramento's VA Northern California Health Care System and Tucson's Southern Arizona VA Health Care System among other medical centres."

Answered by AI

Who meets the criteria to be eligible for this trial?

"This medical research is seeking 7421 volunteers who have experienced intimate partner violence (IPV) and are aged between 18 and 100. Preference will be given to female veterans over the age of majority."

Answered by AI

What are the aims of this experiment?

"The primary outcome of this trial will be a comparison between the rate of disclosure at baseline (months 1-3) and the rate during months 7-9. Secondary objectives encompass Change in Adoption of Screening, Maintenance, and Change in Psychosocial Service Use as secondary implementation outcomes, respectively."

Answered by AI
~1680 spots leftby Apr 2025