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The goal of this clinical trial is to develop and evaluate the preliminary efficacy of an intervention to address alcohol use, sexual distress, and sexual assault risk among college women with a history of sexual victimization. The main questions it aims to answer are: 1) what is the feasibility of the recruitment method, research design, interventionist training methods, and delivery of the intervention; 2) does the intervention, relatively to control, the 2- and 4-month follow-up produces reductions in the quantity/frequency of alcohol use and heavy drinking, sexual distress, and sex-related drinking motives, and sexual revictimization. Participants will engage in both individual and group based intervention for alcohol use, sexual distress, and sexual assault risk. Follow-up assessments are completed at 2- and 4-months following program completion. The intervention is compared to a wait list control group who will have the opportunity to complete the program after completing the 4-month follow up.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| AWARE Program | Experimental | The AWARE program addresses alcohol use, sexual distress and sexual revictimization risk. |
|
| Control Group | No Intervention | The comparison is a wait list control group. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AWARE | Behavioral | AWARE addresses alcohol use, sexual distress, and sexual assault risk among college women with a history of sexual victimization. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Alcohol Use | The number of past month drinking days (Minmum = 0, Maximum = 30), average drinks per drinking day (Minmum = 0, Maximum = unspecificed), number of heavy drinking days (Minimum = 0, Maximum = 30), assessed via the Time Line Follow Back, with greater scores meaning worse outcomes. | Change from baseline alcohol use at 4 months. |
| Sexual Distress | Assessed via the Female Sexual Dysfunction Index, Minimum = 2, Maximum = 36 with higher scores meaning worse outcomes, and the Female Sexual Distress Scale, Minimum = 0, Maximum = 52 with lower scores meaning worse outcomes. | Change from overall levels of sexual dysfunction at 4 months. |
| Sexual Victimization | Assessed via the Sexual Experiences Survey. Scored based on frequency and severity, Minumum = 0, Maximum = 63, higher scores means worse outcomes. | Reductions in severity and frequency of victimization in comparison to control at 4 months. |
| Measure | Description | Time Frame |
|---|---|---|
| Sex-Related Drinking Expectancies | Assessed via the Sex Related Alcohol Expectancies, Minimum = 14, Maximum = 70 | Change in sexual related drinking expectancies at 4 months. |
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Inclusion Criteria:
Exclusion Criteria:
The intervention enrolls cis-gender college women.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Rhode Island Hospital | Providence | Rhode Island | 02904 | United States |
Data will be shared using the National Institute of Mental Health Data Archive (NDA).
The research team will submit data on or before the NDA submission due dates (April 1 and October 1 each year) in accordance with the applicable Data Sharing Terms and Conditions of award.
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| ID | Term |
|---|---|
| D000428 | Alcohol Drinking |
| D012735 | Sexual Dysfunction, Physiological |
| ID | Term |
|---|---|
| D004327 | Drinking Behavior |
| D001519 | Behavior |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
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