MedPath

Evaluation of Unstained

Not Applicable
Recruiting
Conditions
Teen Pregnancy Prevention
Interventions
Behavioral: Unstained
Behavioral: Like
Registration Number
NCT06574139
Lead Sponsor
The Policy & Research Group
Brief Summary

The goal of this randomized trial is to learn if the Unstained intervention has a positive impact on the sexual health behaviors of sexually active youth between the ages of 14 and 22 years old who are at risk for or involved in the legal system. The primary research questions it aims to answer are:

* Three months after being offered the intervention, does Unstained impact youth's receipt of sexually transmitted infection testing in the past four months?

* Nine months after being offered the intervention, does Unstained impact youth's frequency of having vaginal and anal sex without condoms in the past four months?

Researchers will compare participants randomized to receive Unstained (treatment group) to participants randomized to receive a control condition that contains no sexual or reproductive health information (control group).

Participants randomized to the treatment group will be offered Unstained as a virtual, individual-based intervention delivered during three \~60 minute sessions over a 3-6 week period. Participants randomized to the control group will be offered a virtually delivered control condition.

Detailed Description

This is an individual-level, randomized control trial to rigorously evaluate the impact of the Unstained intervention. Participant outcomes will be assessed using self-reported, individual-level data gathered using a structured questionnaire administered at three time points: baseline (enrollment); three months post-intervention (five months after baseline); and nine months post-intervention (eleven months after baseline).

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1500
Inclusion Criteria
  • United States resident
  • Owns or has regular access to a personal device with internet access
  • Comfortable reading, speaking, and writing in English
  • Has had vaginal or anal sex in the past 3 months
  • At risk for or involved in the legal system
Exclusion Criteria
  • Currently trying to start a pregnancy
  • Currently in jail or being detained in a facility
  • Enrolled in an ongoing PRG-run TPP study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
UnstainedUnstained-
LikeLike-
Primary Outcome Measures
NameTimeMethod
Receipt of sexually transmitted infection (STI) testing in the past four monthsAssessed three months after the intervention period has ended (five months post-baseline)

Participants are asked the following item:

1) Have you been tested for sexually transmitted infections (STIs) in the past 4 months? The resulting variable is dichotomous with values 0 or 1, where 0 indicates a person who has not received STI testing in the past four months and 1 indicates a person who has received STI testing in the past four months.

Times having vaginal and anal sex without condoms in the past four monthsAssessed nine months after the intervention period has ended (11 months post-baseline)

Participants are asked the following two items:

1. In the past 4 months, how many times have you had vaginal sex without you or your sexual partner using a condom?

2. In the past 4 months, how many times have you had anal sex without you or your sexual partner using a condom? The resulting variable is continuous with values that range from 0 to k, where 0 indicates that a person has not engaged in vaginal and anal sex without a condom in the past four months, and k indicates the number of times the person has engaged in vaginal and anal sex without a condom in the past four months.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

The Policy & Research Group

🇺🇸

New Orleans, Louisiana, United States

The Policy & Research Group
🇺🇸New Orleans, Louisiana, United States
Hilary Demby, MPH
Contact
504-865-1545
hilary@policyandresearch.com
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