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NC Young Women's CoOp

Primary Purpose

Condomless Sex, Human Immunodeficiency Virus (HIV), Sexually Transmitted Infection (STI)

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Face-to-Face Young Women's CoOp (YWC)
mHealth Young Women's CoOp (YWC)
HIV Counseling and Testing
Sponsored by
RTI International
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Condomless Sex focused on measuring Human Immunodeficiency Virus (HIV), Sexually transmitted infections (STI), mHealth, Substance abuse, Violence, Victimization, Sexual Risk

Eligibility Criteria

18 Years - 25 Years (Adult)FemaleAccepts Healthy Volunteers

Selected Inclusion Criteria:

  • Identify as female
  • Identify as Black or African American
  • 18-25 years of age
  • Have used alcohol or drugs in greater quantity or for a longer period of time than intended within the past 30 days

Exclusion Criteria:

  • Participants may not be non-Black/African American

Sites / Locations

  • Durham County Department of Public Health
  • Guilford County Department of Public Health - Greensboro
  • Guilford County Department of Public Health - High Point
  • Wake County Human Services

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Face-to-Face Young Women's CoOp (YWC)

mHealth Young Women's CoOp (YWC)

HIV Counseling and Testing

Arm Description

Participants in this arm will be offered a two-session face-to-face Young Women's CoOp (YWC) intervention.

Participants in this arm will be offered training on the mobile health application mHealth Young Women's CoOp (YWC) and offered tablets with the mHealth application to complete the two-session intervention.

Participants will be offered standard HIV counseling and testing services.

Outcomes

Primary Outcome Measures

Condomless Sex
Self-reported frequency of condomless sex
Condomless Sex
Self-reported frequency of condomless sex
Condomless Sex
Self-reported frequency of condomless sex
Frequency of Substance Use
Frequency of using illicit drugs and alcohol
Frequency of Substance Use
Frequency of using illicit drugs and alcohol
Frequency of Substance Use
Frequency of using illicit drugs and alcohol

Secondary Outcome Measures

Increased Sexual Negotiation
Self-reported ability to negotiate condom use and other safe sexual behavior with a male partner
Increased Sexual Negotiation
Self-reported ability to negotiate condom use and other safe sexual behavior with a male partner
Increased Sexual Negotiation
Self-reported ability to negotiate condom use and other safe sexual behavior with a male partner
Reduced Alcohol and Illicit Drug Use for a Subsample of Participants
Self-reported amount of alcohol consumption and drugs used; Urine drug screen will be used to test for recent illicit drug use; Breathalyzer test results will be used to assess recent alcohol use
Reduced Alcohol and Illicit Drug Use for a Subsample of Participants
Self-reported amount of alcohol consumption and drugs used; Urine drug screen will be used to test for recent illicit drug use; Breathalyzer test results will be used to assess recent alcohol use
Reduced Alcohol and Illicit Drug Use for a Subsample of Participants
Self-reported amount of alcohol consumption and drugs used; Urine drug screen will be used to test for recent illicit drug use; Breathalyzer test results will be used to assess recent alcohol use
Reduced Violence and Victimization for a Subsample of Participants
Self-reported experiences of emotional, physical, and sexual abuse
Reduced Violence and Victimization for a Subsample of Participants
Self-reported experiences of emotional, physical, and sexual abuse
Reduced Violence and Victimization for a Subsample of Participants
Self-reported experiences of emotional, physical, and sexual abuse

Full Information

First Posted
November 14, 2016
Last Updated
March 21, 2021
Sponsor
RTI International
Collaborators
Durham County Department of Public Health, Guilford County Department of Public Health, Wake County Human Services
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1. Study Identification

Unique Protocol Identification Number
NCT02965014
Brief Title
NC Young Women's CoOp
Official Title
Young Women-Focused HIV Prevention: Seek & Test in North Carolina (NC) Clinics
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
Due to the COVID-19 pandemic, this health department-based trial ended early to limit utilizing clinic services and resources and to ensure participant and staff safety. This termination primarily affected the 12-month follow-up appointments.
Study Start Date
January 18, 2017 (Actual)
Primary Completion Date
March 17, 2020 (Actual)
Study Completion Date
March 17, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
RTI International
Collaborators
Durham County Department of Public Health, Guilford County Department of Public Health, Wake County Human Services

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
This three-arm cross-over randomized trial will develop, test, and compare the efficacy of two delivery formats of the Young Women's CoOp (YWC), which is designed to provide risk reduction and empowerment skills, as well as linkages to healthcare services for women who use substances. The current study will develop a revised version of the YWC and evaluate the relative efficacy of a face-to-face (face-to-face YWC), mobile Health application (mHealth YWC) delivery format, and HIV counseling and testing (HCT) as a control to reduce risky sexual behaviors and reduce substance use among young (18-25) African American women who use substances and are sexually active and have not recently been tested for HIV in three NC counties.
Detailed Description
The purpose of this study is to use the seek, test, treat, and retain framework to develop and test the efficacy of a clinic-based, age-appropriate, woman-focused HIV risk-reduction intervention to reduce sexual risk among up to 700 young sexually active African American women aged 18 to 25 who use drugs in three North Carolina counties. The researchers will test the delivery of the woman-focused intervention conducted in two formats, face-to-face YWC and mHealth YWC, using a three-arm cross-over randomized design in which counties are randomized to (1) HCT as the control, (2) face-to-face YWC; and (3) mHealth YWC that will be delivered on tablets using an interactive app. The researchers will fulfill the purpose of this study through the following aims: (Aim 1) To develop a new YWC intervention and recruitment strategies using formative methods to engage young African American women who use substances and have not recently been tested for HIV, clinic staff, and stakeholders to ensure age appropriateness, to identify barriers to reaching these young women and the challenges in conducting the intervention in the clinics, and to develop the mHealth YWC; (Aim 2) To test the efficacy of two formats of the woman-focused intervention program (face-to-face YWC and mHealth YWC) relative to HCT with up to 700 young women aged 18 to 25 in three North Carolina county health departments for primary outcomes at 6-, and 12-month follow-up assessments; (Aim 3) To estimate the total costs of implementing the face-to-face YWC and mHealth YWC interventions, and to assess the resource components that drive these costs; and (Aim 4) To examine the extent to which the face-to-face YWC and mHealth YWC are perceived by collaborating health clinic staff and participants as being acceptable and sustainable.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Condomless Sex, Human Immunodeficiency Virus (HIV), Sexually Transmitted Infection (STI), Alcohol and Drug Use
Keywords
Human Immunodeficiency Virus (HIV), Sexually transmitted infections (STI), mHealth, Substance abuse, Violence, Victimization, Sexual Risk

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
652 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Face-to-Face Young Women's CoOp (YWC)
Arm Type
Experimental
Arm Description
Participants in this arm will be offered a two-session face-to-face Young Women's CoOp (YWC) intervention.
Arm Title
mHealth Young Women's CoOp (YWC)
Arm Type
Experimental
Arm Description
Participants in this arm will be offered training on the mobile health application mHealth Young Women's CoOp (YWC) and offered tablets with the mHealth application to complete the two-session intervention.
Arm Title
HIV Counseling and Testing
Arm Type
Active Comparator
Arm Description
Participants will be offered standard HIV counseling and testing services.
Intervention Type
Behavioral
Intervention Name(s)
Face-to-Face Young Women's CoOp (YWC)
Intervention Description
Participants will be offered HIV counseling and testing (HCT) and a two-session face-to-face YWC intervention. The face-to-face sessions will include information addressing the intersection of substance use, sexual risk, and violence through skill building, role-play, and rehearsal.
Intervention Type
Behavioral
Intervention Name(s)
mHealth Young Women's CoOp (YWC)
Intervention Description
Participants will be offered HIV counseling and testing (HCT) and training on the mHealth application, which will include all content addressed in the face-to-face YWC delivery format. Participants will also be offered a tablet to complete the two-session intervention.
Intervention Type
Behavioral
Intervention Name(s)
HIV Counseling and Testing
Intervention Description
Participants will be offered standard HIV counseling and testing (HCT).
Primary Outcome Measure Information:
Title
Condomless Sex
Description
Self-reported frequency of condomless sex
Time Frame
Baseline
Title
Condomless Sex
Description
Self-reported frequency of condomless sex
Time Frame
6-month follow-up
Title
Condomless Sex
Description
Self-reported frequency of condomless sex
Time Frame
12-month follow-up
Title
Frequency of Substance Use
Description
Frequency of using illicit drugs and alcohol
Time Frame
Baseline
Title
Frequency of Substance Use
Description
Frequency of using illicit drugs and alcohol
Time Frame
6-month follow-up
Title
Frequency of Substance Use
Description
Frequency of using illicit drugs and alcohol
Time Frame
12-month follow-up
Secondary Outcome Measure Information:
Title
Increased Sexual Negotiation
Description
Self-reported ability to negotiate condom use and other safe sexual behavior with a male partner
Time Frame
Baseline
Title
Increased Sexual Negotiation
Description
Self-reported ability to negotiate condom use and other safe sexual behavior with a male partner
Time Frame
6-month follow-up
Title
Increased Sexual Negotiation
Description
Self-reported ability to negotiate condom use and other safe sexual behavior with a male partner
Time Frame
12-month follow-up
Title
Reduced Alcohol and Illicit Drug Use for a Subsample of Participants
Description
Self-reported amount of alcohol consumption and drugs used; Urine drug screen will be used to test for recent illicit drug use; Breathalyzer test results will be used to assess recent alcohol use
Time Frame
Baseline
Title
Reduced Alcohol and Illicit Drug Use for a Subsample of Participants
Description
Self-reported amount of alcohol consumption and drugs used; Urine drug screen will be used to test for recent illicit drug use; Breathalyzer test results will be used to assess recent alcohol use
Time Frame
6-month follow-up
Title
Reduced Alcohol and Illicit Drug Use for a Subsample of Participants
Description
Self-reported amount of alcohol consumption and drugs used; Urine drug screen will be used to test for recent illicit drug use; Breathalyzer test results will be used to assess recent alcohol use
Time Frame
12-month follow-up
Title
Reduced Violence and Victimization for a Subsample of Participants
Description
Self-reported experiences of emotional, physical, and sexual abuse
Time Frame
Baseline
Title
Reduced Violence and Victimization for a Subsample of Participants
Description
Self-reported experiences of emotional, physical, and sexual abuse
Time Frame
6-month follow-up
Title
Reduced Violence and Victimization for a Subsample of Participants
Description
Self-reported experiences of emotional, physical, and sexual abuse
Time Frame
12-month follow-up

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Selected Inclusion Criteria: Identify as female Identify as Black or African American 18-25 years of age Have used alcohol or drugs in greater quantity or for a longer period of time than intended within the past 30 days Exclusion Criteria: Participants may not be non-Black/African American
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wendee Wechsberg, PhD
Organizational Affiliation
RTI International
Official's Role
Principal Investigator
Facility Information:
Facility Name
Durham County Department of Public Health
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27701
Country
United States
Facility Name
Guilford County Department of Public Health - Greensboro
City
Greensboro
State/Province
North Carolina
ZIP/Postal Code
27405
Country
United States
Facility Name
Guilford County Department of Public Health - High Point
City
High Point
State/Province
North Carolina
ZIP/Postal Code
27260
Country
United States
Facility Name
Wake County Human Services
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27610
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Analytic data sets will be prepared in accordance with the "Privacy Rule" of the Health Insurance Portability and Accountability Act (HIPAA; http://www.hhs.gov/ocr/) as "limited data sets" in which names and other personal health identifiers are removed, birthdays have been converted to age at intake, and other dates have been changed to be days before or after the date of intake. Because there are fewer than 20,000 people in the data set, HIPAA says we cannot ensure that it is completely "de-identified"; consequently, HIPAA requires that we treat it as a "limited data set" and that we have a data sharing agreement (DSA) in place before giving anyone access to the client-level data. After the main findings are published, we will welcome other researchers who want to analyze the data in other ways. Requesting access to data will involve drafting an abstract, checking the feasibility relative to the available data, and seeking the permission of the PI and her team.
Citations:
PubMed Identifier
30081868
Citation
Browne FA, Wechsberg WM, Kizakevich PN, Zule WA, Bonner CP, Madison AN, Howard BN, Turner LB. mHealth versus face-to-face: study protocol for a randomized trial to test a gender-focused intervention for young African American women at risk for HIV in North Carolina. BMC Public Health. 2018 Aug 6;18(1):982. doi: 10.1186/s12889-018-5796-8.
Results Reference
derived

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NC Young Women's CoOp

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