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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04494477
Other study ID # PhilliberINclued
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 22, 2017
Est. completion date March 30, 2020

Study information

Verified date July 2020
Source Philliber Research & Evaluation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The INclued program was implemented in 16 states across the US. The purpose of this study is to measure: Nine months after the end of the program and one year after the workshop, are IN•clued participants less likely to report engaging in risky sexual behavior in the past three months compared to control group participants?


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
The IN•clued program
The INclued program as previously described.

Locations

Country Name City State
United States Philliber Research & Evaluation Accord New York

Sponsors (3)

Lead Sponsor Collaborator
Philliber Research & Evaluation Planned Parenthood of the Great Northwest and the Hawaiian Islands, The Office of Adolescent Health, HHS

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Nine months after the end of the program are IN•clued participants less likely to report engaging in risky sexual behavior in the past three months compared to control group participants? If participants had recent (in the past three months) vaginal sex without a condom or birth control, recent oral sex without protection, or recent anal sex without a condom, they were coded as having engaged in recent unprotected or risky sexual behavior. One year after baseline
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