Computerized intervention for reducing intimate partner victimization for perinatal women seeking mental health treatment: A multisite randomized clinical trial protocol.
Female
Humans
Pregnancy
Costs and Cost Analysis
Crime Victims
/ psychology
Empowerment
Intimate Partner Violence
/ prevention & control
Mental Health
Mental Health Services
/ economics
Motivational Interviewing
Psychotherapy
/ economics
Randomized Controlled Trials as Topic
Research Design
Self Efficacy
Multicenter Studies as Topic
Computer delivered brief intervention
Empowerment
Intimate partner violence
Motivational interviewing
Perinatal women
Journal
Contemporary clinical trials
ISSN: 1559-2030
Titre abrégé: Contemp Clin Trials
Pays: United States
ID NLM: 101242342
Informations de publication
Date de publication:
06 2020
06 2020
Historique:
received:
07
01
2020
revised:
09
04
2020
accepted:
14
04
2020
pubmed:
20
4
2020
medline:
5
8
2021
entrez:
20
4
2020
Statut:
ppublish
Résumé
Intimate partner victimization (IPV) is a significant social and public health problem among perinatal women. Research suggests that 21% to 33% of perinatal women report IPV and there is an enormous amount of morbidity associated with IPV. Moreover, IPV places women at high risk for several psychiatric disorders, which transforms the perinatal period from an already challenging process into a potentially overwhelming one. Further, IPV and untreated mental illness during the perinatal period pose a dual risk of adverse physical and emotional outcomes for women and their developing fetus/infant. Given the high rates of IPV among women who seek mental health treatment, mental health clinics compared to other medical settings are more effective sites for focused case finding and intervention. Our team has successfully tested an innovative, computerized intervention, Strength for U in Relationship Empowerment (SURE). SURE is a brief, interactive program consistent with motivational interviewing and incorporates empowerment strategies. The proposed multisite randomized clinical trial (N = 186) will test whether SURE relative to control is associated with reduced IPV, greater positive affect and well-being, and greater perceived emotional support. We will also evaluate the role of theoretical mediators of empowerment and self-efficacy. Finally, we will estimate the resources needed and costs to deliver SURE, as well as the incremental cost effectiveness of SURE compared with treatment as usual. If SURE is found to be efficacious and cost effective, it can be easily integrated into clinical care and will fill a critical gap for a vulnerable, high-risk population.
Identifiants
pubmed: 32305456
pii: S1551-7144(20)30089-6
doi: 10.1016/j.cct.2020.106011
pmc: PMC7254924
mid: NIHMS1587460
pii:
doi:
Types de publication
Clinical Trial Protocol
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
106011Subventions
Organisme : NICHD NIH HHS
ID : R01 HD094801
Pays : United States
Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no competing interests.
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