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RPCW for Sexual Assault (RPCW Trial)
N/A
Waitlist Available
Led By ParksMarsh A Kathleen, PhD
Research Sponsored by State University of New York at Buffalo
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline to post-intervention (approximately 1 to 2-weeks); change from post-intervention to 3-month follow up; change from 3- to 6-month follow up
Awards & highlights
RPCW Trial Summary
This trial is testing a new intervention to reduce the risk of sexual revictimization for college women. The intervention includes online education modules and in-person group skills training focused on problem solving and behavioral rehearsal. The trial will include 96 women and follow them for 6 months to see if the intervention is effective.
RPCW Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline to post-intervention (approximately 1 to 2-weeks); change from post-intervention to 3-month follow up; change from 3- to 6-month follow up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline to post-intervention (approximately 1 to 2-weeks); change from post-intervention to 3-month follow up; change from 3- to 6-month follow up
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in ability to perceive sexual assault risk cues
Change in number of hazardous drinking days per week
Change in the total number of hazardous drinking days over the past month
+1 moreSecondary outcome measures
Change in state emotion regulation
Change in the use of dating protective strategies
Change in the use of drinking protective behavioral strategies
+1 moreRPCW Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Revictimization Prevention for College Women (RPCW)Experimental Treatment1 Intervention
Active intervention that includes information to reduce hazardous drinking and increase sexual assault risk perception.
Group II: Health Education Control (HEC)Active Control1 Intervention
Time and attention control.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
RPCW
2022
N/A
~60
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Who is running the clinical trial?
State University of New York at BuffaloLead Sponsor
246 Previous Clinical Trials
49,429 Total Patients Enrolled
1 Trials studying Sexual Assault
102 Patients Enrolled for Sexual Assault
National Institute on Alcohol Abuse and Alcoholism (NIAAA)NIH
799 Previous Clinical Trials
1,362,452 Total Patients Enrolled
3 Trials studying Sexual Assault
495 Patients Enrolled for Sexual Assault
ParksMarsh A Kathleen, PhDPrincipal InvestigatorSUNY Buffalo
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have been drinking heavily in the past month, which means having 4 or more drinks at least once in the last 30 days.You have a serious mental illness, like severe depression, schizophrenia, or bipolar disorder.You have thoughts of hurting yourself or others.You have had a prior substance abuse issue since you were 14 years old or younger.
Research Study Groups:
This trial has the following groups:- Group 1: Revictimization Prevention for College Women (RPCW)
- Group 2: Health Education Control (HEC)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- 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
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