- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02647710
PHAT Life: Preventing HIV/AIDS Among Teens in Juvenile Justice (PHAT Life)
30 aprile 2018 aggiornato da: 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.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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 di studio
Interventistico
Iscrizione (Effettivo)
349
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Illinois
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Chicago, Illinois, Stati Uniti, 60612
- University of Illinois at Chicago
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
Da 13 anni a 17 anni (Bambino)
Accetta volontari sani
Sì
Sessi ammissibili allo studio
Tutto
Descrizione
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)
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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
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Comparatore attivo: 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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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in HIV/STI Risk Behaviors at 6 and 12 months
Lasso di tempo: 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
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in HIV/AIDS/STI Knowledge, Attitudes, Beliefs, and Behavioral Skills at 6 and 12 months
Lasso di tempo: Baseline, 6-months, and 12-months
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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
Lasso di tempo: Baseline, 6-months, and 12-months
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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).
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Baseline, 6-months, and 12-months
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Change in Partner Sexual Communication at 6 and 12 months
Lasso di tempo: Baseline, 6-months, and 12-months
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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
Lasso di tempo: Baseline, 6-months, and 12-months
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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.
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Baseline, 6-months, and 12-months
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Change in trauma symptoms and violence exposure at 6 and 12 months
Lasso di tempo: Baseline, 6-months, and 12-months
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The UCLA PTSD Index will measure exposure to trauma and violence.
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Baseline, 6-months, and 12-months
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Change in peer influences at 6 and 12 months
Lasso di tempo: Baseline, 6-months, and 12-months
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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
Lasso di tempo: Baseline, 6-months, and 12-months
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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
Lasso di tempo: Baseline, 6-months, and 12-months
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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
Lasso di tempo: 12-months
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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
Lasso di tempo: 12-months
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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
Lasso di tempo: 12-months
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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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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Investigatori
- Investigatore principale: Geri DONENBERG, PhD, University of Illinois at Chicago
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
Pubblicazioni generali
- 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.
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
15 giugno 2010
Completamento primario (Effettivo)
15 luglio 2016
Completamento dello studio (Effettivo)
31 dicembre 2017
Date di iscrizione allo studio
Primo inviato
29 dicembre 2015
Primo inviato che soddisfa i criteri di controllo qualità
4 gennaio 2016
Primo Inserito (Stima)
6 gennaio 2016
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
3 maggio 2018
Ultimo aggiornamento inviato che soddisfa i criteri QC
30 aprile 2018
Ultimo verificato
1 aprile 2018
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Infezioni da virus a RNA
- Malattie virali
- Infezioni
- Infezioni a trasmissione ematica
- Malattie trasmissibili
- Malattie sessualmente trasmissibili, virali
- Malattie trasmesse sessualmente
- Infezioni da lentivirus
- Infezioni da retroviridae
- Sindromi da deficit immunologico
- Malattie del sistema immunitario
- Malattie da virus lenti
- Infezioni da HIV
- Sindrome da immunodeficienza acquisita
Altri numeri di identificazione dello studio
- R01MD005861 (Sovvenzione/contratto NIH degli Stati Uniti)
- 5R01MD005861-05 (Sovvenzione/contratto NIH degli Stati Uniti)
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su HIV
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Federal University of São PauloGilead SciencesCompletato
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University of MinnesotaRitiratoInfezioni da HIV | HIV/AIDS | HIV | AIDS | Problema di Aids/Hiv | AIDS e infezioniStati Uniti
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National Institute of Allergy and Infectious Diseases...Duke University; Department of Health and Human Services (HHS)Non ancora reclutamento
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Jecho Biopharmaceuticals Co., Ltd.Non ancora reclutamento
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Boston UniversityBill and Melinda Gates Foundation; HE2RO, University of the WitwatersrandReclutamento
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National Institute of Allergy and Infectious Diseases...National Institutes of Health (NIH); Department of Health and Human ServicesReclutamento
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University of California, Los AngelesNational Institute of Mental Health (NIMH); Partners in Hope, Inc.Reclutamento
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Kelley-Ross & Associates, Inc.Gilead SciencesAttivo, non reclutante
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RTI InternationalNational Institute of Mental Health (NIMH); University of Washington; MU-JHU CAREReclutamento
Prove cliniche su PHAT Life Intervention
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University of Illinois at ChicagoNational Institute on Minority Health and Health Disparities (NIMHD)Completato
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University of Alabama, TuscaloosaNational Institute of Nursing Research (NINR)CompletatoDolore | Cure palliative | Disturbi della ritenzione, cognitivi | Altre malattie cronicheStati Uniti
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Oregon Research Behavioral Intervention Strategies...University of Illinois at ChicagoCompletatoInfezione da HIV | Infezioni trasmesse sessualmente | ImplementazioneStati Uniti
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McGill University Health Centre/Research Institute...Quebec Breast Cancer FoundationNon ancora reclutamentoCancro al seno | SopravvivenzaCanada
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University of ZurichETH Zurich (Switzerland)Reclutamento
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Oregon Health and Science UniversityNational Institute of Mental Health (NIMH); University of Connecticut; University... e altri collaboratoriNon ancora reclutamento
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Superior UniversityAttivo, non reclutanteArtrosi al ginocchioPakistan
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Woebot HealthCompletatoComprendere le caratteristiche degli utenti di interventi di salute mentale digitale in relazione agli esiti di salute mentaleStati Uniti
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KK Women's and Children's HospitalCompletatoCambio di pesoSingapore
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San Diego State UniversityUniversity of California, San FranciscoIscrizione su invitoCondizione di controllo | Condizione di interventoStati Uniti