search
Back to results

Mitigating PTSD-CUD After Sexual Assault (RISE-C)

Primary Purpose

Posttraumatic Stress Disorder, Cannabis Use Disorder

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
RISE Guide
Relaxation Control
Sponsored by
University of Nevada, Las Vegas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Posttraumatic Stress Disorder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Women sexual assault survivors presenting for emergency care <72 hours post-assault at 1 of our 4 emergency care sites English speakers 18+ years of age Able to provide informed consent Have a smartphone with continuous service >1 year Report >1x/weekly cannabis use on a substance use screener Report elevated AS (>17 on the Anxiety Sensitivity Index-3) Exclusion Criteria: Inability to provide informed consent (e.g., serious injury preventing the ability to hear, speak, or see to consent and participate, or other causes (e.g., diagnosed cognitive deficits, diagnosed dementia, asleep at time of screening)). Prisoner Currently pregnant Lives with assailant and plans to continue to do so Admitted patient No mailing address Previously enrolled No sexual assault nurse examiner (SANE) examination Reporting current plan and intent for suicide or homicide Does not understand written and spoken English

Sites / Locations

  • University Medical Center
  • UNC Chapel Hill
  • Tulsa Forensic Nursing
  • SAFE Austin

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

RISE Guide

Relaxation

Arm Description

Brief cognitive behavioral intervention completed in the 3 weeks post-assault delivered via Internet on participants' smartphones targeting anxiety sensitivity, or fear of anxious arousal. Patients learn psychoeducation regarding the nature of stress, cognitive retraining to reduce negative interpretations of stress, and how to complete interoceptive exposures to reduce anxiety sensitivity. These skills are supported by 6 concurrent then subsequent weeks of ecological momentary intervention to deliver personalized intervention reminders based on symptoms.

Patients will download the "Breathe2Relax" app, which delivers information about how to use diaphragm breathing (taking slow, deep breaths through the diaphragm) to manage stress. Participants will receive reminders to engage with the intervention. Participants will also receive ecological momentary intervention reminders to engage with the relaxation intervention.

Outcomes

Primary Outcome Measures

Anxiety Sensitivity Index-3 (ASI-3)
18-item self-report measure of anxiety sensitivity assessing all three subdomains of anxiety sensitivity (physical, cognitive, social). Participants respond to 18 items (e.g., It scares me when my heart beats rapidly) on a 4-point Likert scale. Scores range from 0-72, with higher scores indicating higher levels of anxiety sensitivity.

Secondary Outcome Measures

Marijuana Problems Scale (MPS)
19-item self-report measure of problems related to cannabis use (e.g., problems with work, school, social functioning). Participants rate 19 items on a 3- point Likert scale. Scores range from 0 to 38, with higher scores indicating more problems related to cannabis use.
Marijuana Motives Measure - Coping
The MMM is a 25-item self-report measure of cannabis motives, including coping-oriented motives for cannabis use. Participants respond to a list of motives (e.g., to forget my worries, to get high) on a 5-point Likert scale. Scores range from 25 to 125 for the entire measure, with higher scores indicating higher levels of various types of marijuana motives. The primary motive that will be used as an outcome is coping motives (scores range from 4 to 20 on this subscale).
Patient Reported Outcome Measurement Information System - Anxiety Measurement Information System (PROMIS) Anxiety and Depression
7-items assessing self-reported symptoms of anxiety (e.g., anxious, worried, nervous) rated on a 5-point scale. Scores range from 7 to 35, with higher scores indicating higher levels of anxiety. T-scores are used for final scoring.
Patient Reported Outcome Measurement Information System - Depression Measurement Information System (PROMIS) Anxiety and Depression
8 items assessing self-reported symptoms of depression (e.g., worthlessness, helplessness, sadness) rated on a 5-point scale. Scores range from 8 to 40, with higher scores indicating higher levels of depression. T-scores are used for final scoring.
Cannabis Use Frequency
Ecological momentary assessment will include self-report measures of whether or not cannabis was used that day (yes/no). The item will be scored as 0 (no) vs. 1 (yes), with higher scores indicating higher levels of cannabis use frequency.
Cannabis Use Quantity
Ecological momentary assessment will assess quantity of cannabis used on an 8-point scale, assessed 1x/day over 6 weeks. Scores will range from 1-8, with higher scores indicating a higher quantity of cannabis consumed.
Marijuana Cravings - Emotionality Questionnaire
Ecological momentary assessment will include a state version of the emotionality subscale of the Marijuana Cravings Questionnaire. This consists of 4 items rated on a 7-point Likert scale, assessed 4x/day over 6 weeks. Scores range from 4 to 28, with higher scores indicating higher levels of cravings.
PTSD Checklist for Diagnostic and Statistical Manual -5 (DSM-5) (PCL-5)
20-item self-report measure of DSM-5 PTSD symptoms, including 4 symptom clusters of PTSD (re-experiencing, avoidance, negative alterations in cognition and mood, alterations in arousal and reactivity). Participants respond to items corresponding to each DSM-5 symptom of PTSD on a 5-point Likert scale (0 to 4). Scores range from 0 to 80, with higher scores indicating higher levels of PTSD symptoms.

Full Information

First Posted
May 10, 2023
Last Updated
August 10, 2023
Sponsor
University of Nevada, Las Vegas
Collaborators
University of North Carolina, Chapel Hill
search

1. Study Identification

Unique Protocol Identification Number
NCT05989841
Brief Title
Mitigating PTSD-CUD After Sexual Assault
Acronym
RISE-C
Official Title
Mitigating PTSD-CUD Among Women Presenting to Emergency Care After Sexual Assault: Testing a Digital Therapeutic Targeting Anxiety Sensitivity
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 2023 (Anticipated)
Primary Completion Date
May 2028 (Anticipated)
Study Completion Date
May 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nevada, Las Vegas
Collaborators
University of North Carolina, Chapel Hill

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
683,000 women are sexually assaulted annually in the United States, half of whom develop chronic posttraumatic stress disorder (PTSD) and thus have markedly increased risk for cannabis use disorder (CUD). The current proposal will test the acceptability, initial efficacy, and mechanisms underlying a novel digital therapeutic targeting risk for PTSD-CUD, which could address the critical need for PTSD-CUD prevention for the 100,000 women who annually present for emergency care after sexual assault. In this research context, the applicant will receive key training in multisite, emergency-care based randomized clinical trials (RCTs), advanced statistical analyses for RCTs and ecological momentary assessment data, biobehavioral mechanisms underlying PTSD-CUD prevention, and professional development, launching her independent research career focused on reducing the public health burden of PTSD-CUD among sexual assault survivors by leveraging digital therapeutics.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorder, Cannabis Use Disorder

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
RISE Guide
Arm Type
Experimental
Arm Description
Brief cognitive behavioral intervention completed in the 3 weeks post-assault delivered via Internet on participants' smartphones targeting anxiety sensitivity, or fear of anxious arousal. Patients learn psychoeducation regarding the nature of stress, cognitive retraining to reduce negative interpretations of stress, and how to complete interoceptive exposures to reduce anxiety sensitivity. These skills are supported by 6 concurrent then subsequent weeks of ecological momentary intervention to deliver personalized intervention reminders based on symptoms.
Arm Title
Relaxation
Arm Type
Active Comparator
Arm Description
Patients will download the "Breathe2Relax" app, which delivers information about how to use diaphragm breathing (taking slow, deep breaths through the diaphragm) to manage stress. Participants will receive reminders to engage with the intervention. Participants will also receive ecological momentary intervention reminders to engage with the relaxation intervention.
Intervention Type
Behavioral
Intervention Name(s)
RISE Guide
Intervention Description
Brief cognitive behavioral intervention completed in the 3 weeks post-assault delivered via Internet on participants' smartphones targeting anxiety sensitivity, or fear of anxious arousal. Patients learn psychoeducation regarding the nature of stress, cognitive retraining to reduce negative interpretations of stress, and how to complete interoceptive exposures to reduce anxiety sensitivity. These skills are supported by 6 concurrent then subsequent weeks of ecological momentary intervention to deliver personalized intervention reminders based on symptoms.
Intervention Type
Behavioral
Intervention Name(s)
Relaxation Control
Intervention Description
Patients will download the "Breathe2Relax" app, which delivers information about how to use diaphragm breathing (taking slow, deep breaths through the diaphragm) to manage stress. Participants will receive reminders to engage with the intervention. Participants will also receive ecological momentary intervention reminders to engage with the relaxation intervention.
Primary Outcome Measure Information:
Title
Anxiety Sensitivity Index-3 (ASI-3)
Description
18-item self-report measure of anxiety sensitivity assessing all three subdomains of anxiety sensitivity (physical, cognitive, social). Participants respond to 18 items (e.g., It scares me when my heart beats rapidly) on a 4-point Likert scale. Scores range from 0-72, with higher scores indicating higher levels of anxiety sensitivity.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Marijuana Problems Scale (MPS)
Description
19-item self-report measure of problems related to cannabis use (e.g., problems with work, school, social functioning). Participants rate 19 items on a 3- point Likert scale. Scores range from 0 to 38, with higher scores indicating more problems related to cannabis use.
Time Frame
6 months
Title
Marijuana Motives Measure - Coping
Description
The MMM is a 25-item self-report measure of cannabis motives, including coping-oriented motives for cannabis use. Participants respond to a list of motives (e.g., to forget my worries, to get high) on a 5-point Likert scale. Scores range from 25 to 125 for the entire measure, with higher scores indicating higher levels of various types of marijuana motives. The primary motive that will be used as an outcome is coping motives (scores range from 4 to 20 on this subscale).
Time Frame
6 months
Title
Patient Reported Outcome Measurement Information System - Anxiety Measurement Information System (PROMIS) Anxiety and Depression
Description
7-items assessing self-reported symptoms of anxiety (e.g., anxious, worried, nervous) rated on a 5-point scale. Scores range from 7 to 35, with higher scores indicating higher levels of anxiety. T-scores are used for final scoring.
Time Frame
6 months
Title
Patient Reported Outcome Measurement Information System - Depression Measurement Information System (PROMIS) Anxiety and Depression
Description
8 items assessing self-reported symptoms of depression (e.g., worthlessness, helplessness, sadness) rated on a 5-point scale. Scores range from 8 to 40, with higher scores indicating higher levels of depression. T-scores are used for final scoring.
Time Frame
6 months
Title
Cannabis Use Frequency
Description
Ecological momentary assessment will include self-report measures of whether or not cannabis was used that day (yes/no). The item will be scored as 0 (no) vs. 1 (yes), with higher scores indicating higher levels of cannabis use frequency.
Time Frame
6 weeks
Title
Cannabis Use Quantity
Description
Ecological momentary assessment will assess quantity of cannabis used on an 8-point scale, assessed 1x/day over 6 weeks. Scores will range from 1-8, with higher scores indicating a higher quantity of cannabis consumed.
Time Frame
6 weeks
Title
Marijuana Cravings - Emotionality Questionnaire
Description
Ecological momentary assessment will include a state version of the emotionality subscale of the Marijuana Cravings Questionnaire. This consists of 4 items rated on a 7-point Likert scale, assessed 4x/day over 6 weeks. Scores range from 4 to 28, with higher scores indicating higher levels of cravings.
Time Frame
6 weeks
Title
PTSD Checklist for Diagnostic and Statistical Manual -5 (DSM-5) (PCL-5)
Description
20-item self-report measure of DSM-5 PTSD symptoms, including 4 symptom clusters of PTSD (re-experiencing, avoidance, negative alterations in cognition and mood, alterations in arousal and reactivity). Participants respond to items corresponding to each DSM-5 symptom of PTSD on a 5-point Likert scale (0 to 4). Scores range from 0 to 80, with higher scores indicating higher levels of PTSD symptoms.
Time Frame
6 months

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Assigned female at birth and currently identifying as female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women sexual assault survivors presenting for emergency care <72 hours post-assault at 1 of our 4 emergency care sites English speakers 18+ years of age Able to provide informed consent Have a smartphone with continuous service >1 year Report >1x/weekly cannabis use on a substance use screener Report elevated AS (>17 on the Anxiety Sensitivity Index-3) Exclusion Criteria: Inability to provide informed consent (e.g., serious injury preventing the ability to hear, speak, or see to consent and participate, or other causes (e.g., diagnosed cognitive deficits, diagnosed dementia, asleep at time of screening)). Prisoner Currently pregnant Lives with assailant and plans to continue to do so Admitted patient No mailing address Previously enrolled No sexual assault nurse examiner (SANE) examination Reporting current plan and intent for suicide or homicide Does not understand written and spoken English
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nicole A Short, PhD
Phone
7028950606
Email
nicole.short@unlv.edu
Facility Information:
Facility Name
University Medical Center
City
Las Vegas
State/Province
Nevada
ZIP/Postal Code
89102
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jordana Haber, MD
Phone
702-383-2000
Email
jordana.haber@unlv.edu
First Name & Middle Initial & Last Name & Degree
Jordana Haber, MD
Facility Name
UNC Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karen Serrano, MD
Phone
919-966-6442
Email
kserrano@email.unc.edu
First Name & Middle Initial & Last Name & Degree
Karen Serrano, MD
Facility Name
Tulsa Forensic Nursing
City
Tulsa
State/Province
Oklahoma
ZIP/Postal Code
74103
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kasey Magness, BSN
Phone
918-743-5763
Email
kmagness@cityoftulsa.org
First Name & Middle Initial & Last Name & Degree
Kasey Magness, BSN
Facility Name
SAFE Austin
City
Austin
State/Province
Texas
ZIP/Postal Code
74103
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jenny Black, BSN
Phone
512-267-7233
Email
jblack@safeaustin.org
First Name & Middle Initial & Last Name & Degree
Jenny Black, BSN

12. IPD Sharing Statement

Learn more about this trial

Mitigating PTSD-CUD After Sexual Assault

We'll reach out to this number within 24 hrs