Tools for Health and Resilience Implemented After Violence Exposure (Project THRIVE)

Preventing Risky Drinking and PTSD After Sexual Assault: A Web-Based Intervention

Sexual assault victimization is a common and particularly harmful form of trauma that is associated with increased risk for high-risk drinking and other conditions of public health concern, such as PTSD. Given evidence that sexual assault survivors who have low social support or receive negative social reactions to sexual assault disclosure are more likely to experience PTSD and drinking problems, improving social support is a novel target for intervention. The proposed study will attempt to prevent the onset of high-risk drinking and PTSD in sexual assault survivors by developing and testing a web-based early intervention aimed at increasing contact with social supporters and mitigating the harm of negative social reactions; ultimately, results will contribute to advancing the field's understanding of the potential for social support to mitigate the harm of trauma.

Study Overview

• Status: Completed
• Conditions: Post Traumatic Stress Disorder; Problem Drinking
• Intervention / Treatment: Behavioral: App-based intervention

Detailed Description

This study involves developing, modifying, and preliminarily testing an intervention to prevent high-risk drinking and PTSD in women who have experienced sexual assault (SA) in the past 10 weeks. In the pilot trial phase of this study, intervention feasibility will be tested in an open trial with N = 40 women with past-10-week SA histories, active drinking, and elevated distress. Participants will complete surveys at baseline, termination, and 3-month follow-up. Participants will be randomized to either the intervention (N = 20) or assessment-only control (N = 20). We hypothesize that (H1) most participants will respond positively on items assessing satisfaction with the intervention, (H2) participants will report above-average usability on a standardized measure, (H3) completion rates for daily activities will be similar to previous web-based interventions, (H4) participants will show significant learning as evidenced by increases in correct responses to knowledge questions from baseline to post, and (H5) participants in the intervention condition will evidence less high-risk drinking and PTSD at 3-month follow-up than participants in the assessment-only condition.

• Study Type: Interventional
• Enrollment (Actual): 41
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Washington
    • Seattle, Washington, United States, 98105
      • University of Washington School of Medicine

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• informed consent
• self-identification as female
• sexual assault, defined as endorsement of unwanted, attempted or completed sexual contact in the past 10 weeks
• age > 18
• English fluency
• smartphone and internet access at least daily for 3 weeks and at least weekly for 3 months
• consumption of >1 alcoholic drink in the past month
• >1 episode of high-risk drinking in past 6 months, defined as either more than 3 drinks on a given day or more than 7 drinks in a given week
• at least 3 symptom clusters endorsed on the PTSD Checklist.

Exclusion Criteria:

• active suicidality
• psychosis

Study Plan

How is the study designed?

Design Details

• Primary Purpose: PREVENTION
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Intervention; The THRIVE app involves 3 weeks of daily activities. Day 1 involves identification of activities to add to a "self-care activity list" with guidance around selecting activities that increase social contact, reduce alcohol use, and reduce avoidance. They will also complete an active-learning exercise about cognitive distortions and create a "stuck point to-do list" consisting of their cognitive distortions. In subsequent days, participants will be prompted to complete activities from both lists. They will also have access optional activities on topics such as asking for help, preventing isolation, deciding whether to disclose an assault, coping with negative reactions to disclosure, and thinking in helpful ways about social support. They will be prompted to complete brief daily surveys in the app, which will populate a symptom tracker. Participants in will have brief weekly phone contact with a coach to monitor safety and troubleshoot issues with app use.	Behavioral: App-based intervention; A app-based cognitive-behavioral intervention to prevent the development of PTSD and high-risk drinking in recently-victimized adults; Other Names: THRIVE app
NO_INTERVENTION: Assessment-only control; The assessment-only control condition will involve access to a version of the app that includes daily surveys and a symptom tracker populated by these surveys, but without any of the other exercises included in the experimental version of the app. Participants in the control condition will have brief weekly phone contact with a coach to monitor safety and troubleshoot issues with app use.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Problem Drinking Scores at Baseline and 3 Weeks	Sum scores on Rutgers Alcohol Problem Index- Short Form (RAPI-S), which assesses alcohol use consequences. Range: 0-64; higher scores indicate worse outcome.	Baseline, post-intervention (3 weeks after baseline)
Problem Drinking Scores at Baseline and 3 Months	Sum scores on Rutgers Alcohol Problem Index- Short Form (RAPI-S), which assesses alcohol use consequences. Range: 0-64; higher scores indicate worse outcome.	Baseline, 3 month follow-up
Posttraumatic Stress Symptom Severity Score at Baseline and 3 Weeks	Sum scores on the Posttraumatic Stress Disorder Checklist for the Diagnostic and Statistical Manual of Mental Disorders-5 (PCL-5), which assesses posttraumatic stress symptom severity. Range: 0-80; higher scores indicate worse outcome.	Baseline, post-intervention (3 weeks after baseline)
Posttraumatic Stress Symptom Severity Score at Baseline and 3 Months	Sum scores on the Posttraumatic Stress Disorder Checklist for the Diagnostic and Statistical Manual of Mental Disorders-5 (PCL-5), which assesses posttraumatic stress symptom severity. Range: 0-80; higher scores indicate worse outcome.	Baseline, 3 month follow-up

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Anxiety	Sum scores on Generalized Anxiety Disorder-7 (GAD-7), which assesses symptoms of anxiety. Range: 0-21; higher scores indicate worse outcome.	Baseline, post-intervention (3 weeks after baseline), 3 month follow-up
Coping Self-efficacy	Mean scores on the Trauma Coping Self-Efficacy Scale (CSE-T), which assesses one's perceived ability to manage the demands of recovering from a potentially-traumatic event. Range: 1 to 7; higher scores indicate better outcome.	Baseline, post-intervention (3 weeks after baseline), 3 month follow-up
Depression	Sum scores on the Patient Health Questionnaire-8 (PHQ-8), which assesses symptoms of depression. Range: 0-24; higher scores indicate worse outcome.	Baseline, post-intervention (3 weeks after baseline), 3 month follow-up
Alcohol Consumption (Quantity)	Number of drinks per week reported on the Daily Drinking Questionnaire	Baseline, post-intervention (3 weeks after baseline), 3 month follow-up
Alcohol Consumption (Frequency)	Number of drinking days per week reported on the Daily Drinking Questionnaire	Baseline, post-intervention (3 weeks after baseline), 3 month follow-up
Alcohol Consumption (Hours)	Hours spent drinking per week reported on the Daily Drinking Questionnaire	Baseline, post-intervention (3 weeks after baseline), 3 month follow-up

Collaborators and Investigators

• Sponsor: University of Washington
• Collaborators: National Institute on Alcohol Abuse and Alcoholism (NIAAA)
• Investigators: Principal Investigator: Emily Dworkin, PhD, University of Washington

Study record dates

Study Major Dates

• Study Start (ACTUAL): January 13, 2021
• Primary Completion (ACTUAL): August 24, 2021
• Study Completion (ACTUAL): November 20, 2021

Study Registration Dates

• First Submitted: June 11, 2018
• First Submitted That Met QC Criteria: October 9, 2018
• First Posted (ACTUAL): October 11, 2018

Study Record Updates

• Last Update Posted (ACTUAL): December 2, 2022
• Last Update Submitted That Met QC Criteria: November 15, 2022
• Last Verified: November 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Mental Disorders; Trauma and Stressor Related Disorders; Stress Disorders, Traumatic; Stress Disorders, Post-Traumatic
• Other Study ID Numbers: STUDY00005025; R00AA026317 (NIH)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No