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Blended Facilitation for Domestic Violence
Study Summary
This trial will study the effects of a new program to screen women Veterans for intimate partner violence.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- Group 1: Toolkit + Implementation as Usual
- Group 2: Toolkit + Blended Facilitation
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
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."
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."
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."
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."
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."
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