Viewing Study NCT06580080



Ignite Creation Date: 2024-10-26 @ 3:39 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06580080
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-28

Brief Title: Evaluation of Are You Ready
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation of Are You Ready
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: AYR
Brief Summary: The goal of this randomized trial is to learn if the Are You Ready AYR intervention has a positive impact on the sexual and mental health behaviors of sexually active youth between the ages of 14 and 21 years old who are at risk for or involved in the juvenile justice andor child welfare systems The primary research questions it aims to answer are

Three months after being offered the intervention does AYR impact youths receipt of sexually transmitted infection testing in the past three months
Three months after being offered the intervention does AYR impact youths use of coping skills
Nine months after being offered the intervention does AYR impact youths frequency of having vaginal and anal sex without condoms in the past three months

Researchers will compare participants randomized to receive AYR 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 AYR as a virtual or in-person 25 hour group session 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 Are You Ready AYR 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 four months after baseline and nine months post-intervention ten months after baseline

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None