- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02647710
PHAT Life: Preventing HIV/AIDS Among Teens in Juvenile Justice (PHAT Life)
30 avril 2018 mis à jour par: 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.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Interventionnel
Inscription (Réel)
349
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
Illinois
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Chicago, Illinois, États-Unis, 60612
- University of Illinois at Chicago
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-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
13 ans à 17 ans (Enfant)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
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 d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
|
HIV Prevention behavioral health intervention
|
|
Comparateur actif: 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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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in HIV/STI Risk Behaviors at 6 and 12 months
Délai: baseline, 6-months, and 12--months
|
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.
|
baseline, 6-months, and 12--months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in HIV/AIDS/STI Knowledge, Attitudes, Beliefs, and Behavioral Skills at 6 and 12 months
Délai: 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.
|
Baseline, 6-months, and 12-months
|
|
Change in mental health symptoms at 6 and 12 months
Délai: 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
Délai: 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
Délai: 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
Délai: Baseline, 6-months, and 12-months
|
The UCLA PTSD Index will measure exposure to trauma and violence.
|
Baseline, 6-months, and 12-months
|
|
Change in peer influences at 6 and 12 months
Délai: 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
Délai: Baseline, 6-months, and 12-months
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The Parenting Style Questionnaire (PSQ) measures parental supervision, monitoring, and permissiveness.
|
Baseline, 6-months, and 12-months
|
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Change in parental communication at 6 and 12 months
Délai: 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.
|
Baseline, 6-months, and 12-months
|
|
Biological Measure of N. Gonorrhoeae Acquisition
Délai: 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.
|
12-months
|
|
Biological Measure of C. Trachomatis Acquisition
Délai: 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.
|
12-months
|
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Biological Measure of T. Vaginalis Acquisition
Délai: 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.
|
12-months
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Geri DONENBERG, PhD, University of Illinois at Chicago
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Publications générales
- 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.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
15 juin 2010
Achèvement primaire (Réel)
15 juillet 2016
Achèvement de l'étude (Réel)
31 décembre 2017
Dates d'inscription aux études
Première soumission
29 décembre 2015
Première soumission répondant aux critères de contrôle qualité
4 janvier 2016
Première publication (Estimation)
6 janvier 2016
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
3 mai 2018
Dernière mise à jour soumise répondant aux critères de contrôle qualité
30 avril 2018
Dernière vérification
1 avril 2018
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Infections par virus à ARN
- Maladies virales
- Infections
- Infections transmissibles par le sang
- Maladies transmissibles
- Maladies sexuellement transmissibles, virales
- Maladies sexuellement transmissibles
- Infections à lentivirus
- Infections à rétroviridae
- Syndromes d'immunodéficience
- Maladies du système immunitaire
- Maladies à virus lents
- Infections à VIH
- Syndrome immunodéficitaire acquis
Autres numéros d'identification d'étude
- R01MD005861 (Subvention/contrat des NIH des États-Unis)
- 5R01MD005861-05 (Subvention/contrat des NIH des États-Unis)
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .