Development and Pilot Trial of an Intervention to Reduce Disclosure Recipients Negative Social Reactions and Victims Psychological Distress and Problem Drinking



Status:Recruiting
Conditions:Depression, Psychiatric, Psychiatric, Psychiatric, Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 24
Updated:10/19/2018
Start Date:September 10, 2018
End Date:August 28, 2020
Contact:Katie Edwards, PhD
Email:Katie.Edwards@unh.edu
Phone:603-862-3720

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The purpose of this randomized controlled trial is to evaluate an intervention, Supporting
Survivors and Self: An Intervention for Social Supports of Survivors of Partner Abuse and
Sexual Aggression (SSS). SSS trains potential recipients of IPV or SA disclosure on the best
methods of responding to a victim's disclosure. Consenting college students will be
randomized into the SSS intervention or a wait-list control condition. Evaluation data will
be multi-informant (i.e., data from both informal supports and victims) and multi-method
(i.e., qualitative and quantitative). The investigators hypothesize that individuals
receiving the SSS intervention, compared to individuals in the wait-list control condition,
will provide less negative and more positive social reactions to victims' disclosure.

Intimate partner violence (IPV) and sexual assault (SA) are public health issues that impact
the vast majority of college students in some capacity (as a victim and/or disclosure
recipient). Most (75+%) victims disclose to informal supports, such as friends.
Unfortunately, over 80% of victims' disclosures are met with negative social reactions (e.g.,
blame) from informal supports (used interchangeably with disclosure recipients). Negative
social reactions predict deleterious psychological (e.g., posttraumatic stress disorder) and
behavioral (e.g., problem drinking) health outcomes in victims. Although recent research has
shed light on the factors (e.g., victim attributions) that predict informal supports'
negative (e.g., egocentric and blaming statements) and positive (e.g., providing emotional
support) social reactions, there is no intervention to date that targets potential recipients
of IPV and SA disclosure to inform these individuals of the best methods of responding to an
IPV or SA disclosure. This type of intervention, if effective in reducing negative social
reactions in informal supports, could reduce problem drinking and related outcomes in
victims.

Thus, in the current study, the investigators evaluate an intervention (i.e., Supporting
Survivors and Self [SSS]) created for potential informal support disclosure recipients.
College students are the target population for the initial version of the SSS intervention
given the high rates of SA, IPV, and alcohol misuse among this demographic. The interactive,
two-session intervention teaches potential disclosure recipients what to say and not to say
and ways to promote healthy coping and discourage unhealthy coping in victims. The role of
alcohol in risk for and outcomes associated with IPV and SA as well as alcohol-specific
social reactions are addressed in the SSS intervention because alcohol is involved in most
situations of IPV and SA among college students, and drinking to cope is common among
victims.

This study is a small-scale, yet rigorous, initial evaluation of the SSS intervention that
includes a prospective (i.e., intervention prior to potential disclosure) and experimental
(i.e., randomized control trial) methodology. Outcome data will be multi-informant (i.e.,
data from both informal supports and victims) and multi-method (i.e., qualitative and
quantitative). The investigators will:

1. Implement and evaluate the effectiveness of the SSS intervention compared to a wait-list
control condition among potential informal supports. Hypothesis 1a: Individuals
receiving the SSS intervention (N=450) compared to individuals in the wait-list control
condition (N=450) will report fewer IPV and SA rape myths as well as greater intentions
to provide positive social reactions and fewer intentions to provide negative social
reactions. Hypothesis 1b: Individuals who receive SSS intervention and are subsequent
disclosure recipients (n=100) will report providing less negative social reactions and
more positive social reactions than individuals in the control condition who are
subsequent disclosure recipients (n=100); mediators (e.g., low victim blame) and
moderators (e.g., victim alcohol use at time of assault) of outcomes will be examined.
Hypothesis 1c: Individuals who receive the SSS intervention and are subsequent victims
of IPV and/or SA (n=60) will report less self-blame, PTSD, depression, drinking to cope,
and problem drinking compared to individuals in the control condition who are subsequent
victims of IPV and/or SA (n=60); mediators (e.g., engagement in healthy coping) and
moderators (e.g., gender) will be explored. Methodology: A random sample of college
students from a public university will be invited to participate in a pre-test (all
participants), SSS intervention (only participants randomly assigned to this condition),
and six-month post-test (all participants). A subsample of disclosure recipients in the
SSS intervention condition will be invited to participate in a qualitative exit
interviews (after the post-test) to enrich findings and inform SSS revisions.

2. Determine the feasibility in recruiting victims who disclosed to individuals in the SSS
and control conditions to complete outcome surveys and gather preliminary effectiveness
data on the SSS intervention. Hypothesis 2a: Victims who disclose to an individual in
the SSS intervention (n=50) will report trends towards receiving more positive social
reactions to disclosure, less negative social reactions to disclosure, and fewer
symptoms of PTSD, depression, drinking to cope, and negative alcohol-related
consequences compared to individuals who disclose to an individual in the control
condition (n=50).

Inclusion Criteria:

- undergraduate student at University of New Hampshire

- read and understand English

- able to independently complete online surveys
We found this trial at
1
site
Durham, New Hampshire 03824
Phone: 603-862-2360
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Durham, NH
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