- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02647710
PHAT Life: Preventing HIV/AIDS Among Teens in Juvenile Justice (PHAT Life)
30 de abril de 2018 actualizado por: Geri Donenberg, University of Illinois at Chicago
PHAT Life: Preventing HIV/AIDS Among Teens, is a uniquely-tailored intervention designed for recently-arrested juvenile offenders on probation.
The program will teach teens about HIV/AIDS, sexually transmitted infections, and safer decision-making.
The PHAT Life Research Study is a 2-arm randomized controlled trial of the PHAT Life Intervention.
The investigators will test and compare PHAT Life to the health promotion control group on adolescent risky sexual behavior, substance use, and theoretical mediators.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
High rates of mental illness, HIV/AIDS/STI, and incarceration among African Americans (AA) reflect significant health disparities, particularly among youth.
Teens in juvenile justice are disproportionately AA, and compared to the general population, juvenile offenders (JO) report more risky sexual behavior, drug and alcohol use, and psychiatric disorders, and are more likely to test positive for STIs.
Still, few empirically-supported, theoretically-driven programs exist to address their negative health outcomes.
This proposal addresses these health disparities by testing an innovative and uniquely tailored HIV/AIDS/STI, mental health, and substance use program designed for and pilot tested with recently arrested 13 - 17 year-old urban males and females (85% African American, 14% Latino/a) released on probation.
PHAT Life was derived from a carefully staged process that included an active, diverse, multi-disciplinary advisory board, a youth advisory board, focus groups, two pilot tests, extensive feedback, and a series of curriculum revisions over three years.
The R34 established feasibility and acceptability, revealed positive youth and stakeholder feedback, and yielded good preliminary outcomes at 3-month follow-up (e.g., increased condom use) to justify an efficacy trial.
This application proposes a 2-arm randomized controlled trial to test PHAT Life versus a health promotion program with recently arrested 13-17 year-old male and female, mostly ethnic minority JO (as representative of Cook County) on probation in Chicago.
The investigators will use the procedures and methods established in the developmental study to recruit, enroll, assess, track, and intervene with teens.
Investigators will randomly assign youth to PHAT Life (N=150) or a health promotion control group (N=150).
The interventions will be delivered in single sex groups of 5 - 7 teens at Evening Reporting Centers.
Assessments will occur at baseline, 6-, and 12-months post-treatment, and participants will be screened for three common STIs (Chlamydia, Gonorrhea, Trichamonas) at baseline and 12-month follow-up.
All youth who test positive for an STI will receive single dose antibiotic treatment free of charge.
An intent-to-treat analysis will be used to test and compare PHAT Life to the health promotion control group on adolescent risky sexual behavior, substance use, and theoretical mediators.
This study answers a compelling need for innovative prevention programs that address the intersecting health disparities of mental illness and HIV/AIDS/STIs among youth in juvenile justice.
Without intervention, these teens continue to engage in risk behaviors post-release, amplifying their own and their partner's risk for HIV/AIDS/STIs.
The lasting effects on community well-being, individual employment prospects, and neighborhood health are profound, but effective programs can alter the negative developmental trajectories of this very high-risk population and begin to redress existing health disparities.
Tipo de estudio
Intervencionista
Inscripción (Actual)
349
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
-
-
Illinois
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Chicago, Illinois, Estados Unidos, 60612
- University of Illinois at Chicago
-
-
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
13 años a 17 años (Niño)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- male or female gender
- placed on probation following arrest
- remanded to a probation program
- 13-17 years old
- both adolescent and parent are fluent English speakers
- not a ward of the state (DCFS Ward).
Exclusion Criteria:
- are unable to understand the consent/assent process
- do not speak English, because instruments are normed for English speakers
- do not assent; d) legal guardians do not consent to teens' participation
- are not 13 -17 years old
- are not on probation or remanded to a probation program
- are Wards of the state (DCFS Ward)
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: PHAT Life Intervention
PHAT Life: Preventing HIV/AIDS Among Teens, is a uniquely-tailored intervention designed for recently-arrested juvenile offenders on probation.
The program will teach teens about HIV/AIDS, sexually transmitted infections, and safer decision-making.
PHAT Life draws on social learning theory and a Social-Personal Framework to address individual and social mechanisms related to HIV-risk, including emotion regulation, peer norms, partner communication, relationship characteristics, and HIV/AIDS/STI and substance use knowledge, attitudes, and beliefs.
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HIV Prevention behavioral health intervention
|
|
Comparador activo: Health Promotion Control
A health promotion program focusing on nutrition, physical activity, substance use, and sexual health.
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Behavioral health intervention control
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in HIV/STI Risk Behaviors at 6 and 12 months
Periodo de tiempo: baseline, 6-months, and 12--months
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AIDS Risk Behavior Assessment (ARBA) A computer-assisted structured interview of self-reported sexual behavior and drug use derived from five well-established measures.
The outcomes include ever had sex, condom use, number of partners, sex while using drugs and/or alcohol.
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baseline, 6-months, and 12--months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in HIV/AIDS/STI Knowledge, Attitudes, Beliefs, and Behavioral Skills at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
Survey measuring knowledge regarding transmission routes, misconceptions about transmission, and risk-reduction strategies; attitudes and beliefs including peer norms, intentions to prevent HIV/AIDS/STI, attitudes towards preventive actions, and beliefs about condom use; as well as self-efficacy to prevent transmission, apply condoms, and negotiate with a partner.
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Baseline, 6-months, and 12-months
|
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Change in mental health symptoms at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
The Youth Self Report (YSR) is a widely-used and validated measure of child behavior problems that generates raw and T-scores for internalizing and externalizing syndromes as well as narrow-band problems (e.g., delinquency, anxiety, depression).
|
Baseline, 6-months, and 12-months
|
|
Change in Partner Sexual Communication at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
Questionnaire in which participants indicate whether they ever talked to their romantic or dating partners and sexual partners about a list of sexual topics, how often they discussed them, and whether they talk was open and comfortable.
Items were adapted from the Sexual Risk Behavior Questionnaire.
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Baseline, 6-months, and 12-months
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Change in Relationship dynamics at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
The Sexual Relationship Power Scale (SRPS) measures perceptions of relationship control and decision-making dominance.
It has good internal consistency and predictive and constructed validity.
|
Baseline, 6-months, and 12-months
|
|
Change in trauma symptoms and violence exposure at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
The UCLA PTSD Index will measure exposure to trauma and violence.
|
Baseline, 6-months, and 12-months
|
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Change in peer influences at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
The Peer Convention Behavior Questionnaire will measure peer support of risky behavior, peer norms, and peer pressure and teens' association with prosocial peers.
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Baseline, 6-months, and 12-months
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Change in parental Influences at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
The Parenting Style Questionnaire (PSQ) measures parental supervision, monitoring, and permissiveness.
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Baseline, 6-months, and 12-months
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Change in parental communication at 6 and 12 months
Periodo de tiempo: Baseline, 6-months, and 12-months
|
The Parent-Child Sexual Communication Questionnaire assesses youths' perceived quality and quantity of risk-specific communication with their parents.
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Baseline, 6-months, and 12-months
|
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Biological Measure of N. Gonorrhoeae Acquisition
Periodo de tiempo: 12-months
|
Sexually transmitted infections will be measured using biological endpoint (yes/no) to evaluate intervention effects.
Participants will be screened for N. gonorrhoeae and treated if necessary at baseline.
They will be tested again 12 months later to determine rate of STI acquisition.
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12-months
|
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Biological Measure of C. Trachomatis Acquisition
Periodo de tiempo: 12-months
|
Sexually transmitted infections will be measured using biological endpoint (yes/no) to evaluate intervention effects.
Participants will be screened for C. trachomatis and treated if necessary at baseline.
They will be tested again 12 months later to determine rate of STI acquisition.
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12-months
|
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Biological Measure of T. Vaginalis Acquisition
Periodo de tiempo: 12-months
|
Sexually transmitted infections will be measured using biological endpoint (yes/no) to evaluate intervention effects.
Participants will be screened for T. vaginalis and treated if necessary at baseline.
They will be tested again 12 months later to determine rate of STI acquisition.
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12-months
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Geri DONENBERG, PhD, University of Illinois at Chicago
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- Donenberg GR, Emerson E, Mackesy-Amiti ME, Udell W. HIV-Risk Reduction with Juvenile Offenders on Probation. J Child Fam Stud. 2015 Jun 1;24(6):1672-1684. doi: 10.1007/s10826-014-9970-z.
- Udell W, Donenberg G, Emerson E. Parents matter in HIV-risk among probation youth. J Fam Psychol. 2011 Oct;25(5):785-9. doi: 10.1037/a0024987.
- Wilson HW, Berent E, Donenberg GR, Emerson EM, Rodriguez EM, Sandesara A. Trauma History and PTSD Symptoms in Juvenile Offenders on Probation. Vict Offender. 2013;8(4):10.1080/15564886.2013.835296. doi: 10.1080/15564886.2013.835296.
- Donenberg G, Emerson E, Kendall AD. HIV-risk reduction intervention for juvenile offenders on probation: The PHAT Life group randomized controlled trial. Health Psychol. 2018 Apr;37(4):364-374. doi: 10.1037/hea0000582. Epub 2018 Feb 1.
- Kendall AD, Emerson EM, Hartmann WE, Zinbarg RE, Donenberg GR. A Two-Week Psychosocial Intervention Reduces Future Aggression and Incarceration in Clinically Aggressive Juvenile Offenders. J Am Acad Child Adolesc Psychiatry. 2017 Dec;56(12):1053-1061. doi: 10.1016/j.jaac.2017.09.424. Epub 2017 Oct 5.
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
15 de junio de 2010
Finalización primaria (Actual)
15 de julio de 2016
Finalización del estudio (Actual)
31 de diciembre de 2017
Fechas de registro del estudio
Enviado por primera vez
29 de diciembre de 2015
Primero enviado que cumplió con los criterios de control de calidad
4 de enero de 2016
Publicado por primera vez (Estimar)
6 de enero de 2016
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
3 de mayo de 2018
Última actualización enviada que cumplió con los criterios de control de calidad
30 de abril de 2018
Última verificación
1 de abril de 2018
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Infecciones por virus de ARN
- Enfermedades virales
- Infecciones
- Infecciones transmitidas por la sangre
- Enfermedades contagiosas
- Enfermedades De Transmisión Sexual Virales
- Enfermedades de transmisión sexual
- Infecciones por lentivirus
- Infecciones por retroviridae
- Síndromes de deficiencia inmunológica
- Enfermedades del sistema inmunológico
- Enfermedades de virus lentos
- Infecciones por VIH
- Síndrome de inmunodeficiencia adquirida
Otros números de identificación del estudio
- R01MD005861 (Subvención/contrato del NIH de EE. UU.)
- 5R01MD005861-05 (Subvención/contrato del NIH de EE. UU.)
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
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