Strength for U in Relationship Empowerment

  • STATUS
    Recruiting
  • days left to enroll
    37
  • participants needed
    186
  • sponsor
    Women and Infants Hospital of Rhode Island
Updated on 19 February 2024
drug use

Summary

The objective of this study is to test whether the innovative intervention, "Strength for U in Relationship Empowerment" (SURE), reduces the frequency of IPV more than an attention, time, and information matched control condition in perinatal women seeking mental health care.

Description

Intimate partner victimization (IPV) is a significant social and public health problem among perinatal women. IPV places a woman at high risk for several psychiatric disorders, which transforms the perinatal period from an already challenging process into a potentially overwhelming one. IPV and untreated mental illness during the perinatal period poses 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 (e.g. primary care) are more effective sites for focused case finding and intervention. In addition, the presence of IPV increases the likelihood of disengagement from treatment, which could further compromise the health and safety of women and their fetus/infant. Despite the high-risk profile of women with IPV and mental health illness, there are low screening and intervention rates of female mental health patients with IPV within mental health settings.

The objective of this R01 Award is to fill this critical gap by building upon our promising pilot findings to test whether the innovative intervention, "Strength for U in Relationship Empowerment" (SURE), reduces the frequency of IPV more than an attention, time, and information matched control condition in perinatal women seeking mental health care.

The investigators propose a two-group, randomized controlled trial in which 186 perinatal women with IPV women seeking mental health care who will be assigned to either (a) SURE, a computer-delivered, single-session brief intervention plus one interventionist-led phone booster that is consistent with motivational interviewing and informed by the literature on effective interventions for our target population and targeted risk factors, or (b) a computer-delivered control + one interventionist-led phone booster condition. Computer-delivered follow-up assessments will occur at 6 weeks, 3 months, 6 months, and 12 months after the baseline assessment.

Details
Condition Inactivated poliovirus vaccine, mental health, Perinatal
Age 18years - 45years
Treatment Strength for U in Relationship Empowerment (SURE), Attention, time, and information matched control
Clinical Study IdentifierNCT04218864
SponsorWomen and Infants Hospital of Rhode Island
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Pregnant women
Women who have had a baby in the last 6 months
Between the ages of 18 - 45 years old
Have reported partner abuse within the last year as measured by the Woman Abuse Screening Tool (WAST)
Are in treatment or looking for treatment for mental health at one of the study site clinics

Exclusion Criteria

Cannot provide informed consent
Unable to understand English
Clear my responses

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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