A Parent-Based Intervention to Reduce Sexual Risk Behavior in Adolescents
Reducing Teen Sexual Behavior: A Clinic-Based Approach
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
In the United States, racial and ethnic minorities suffer disproportionately from preventable diseases and conditions. Many of these problems result from health-related behaviors that are established during childhood and adolescence. Latino and African-American adolescents are at considerable risk for the negative consequences of early, risky sexual activity. This study will focus on Latino and African-American early adolescents ages 11 to 14.
The primary aim for this study will be to test and refine a triadic intervention developed for healthcare providers and parents to address the issue of sexual risk behavior among African American and Latino adolescents.
The triadic intervention will take place in a pediatric health care clinic when mothers accompany their children for a non-acute care visit. Mothers will meet with a provider extender (medical assistant, social worker, counselor) for approximately 30 minutes while their children are being examined by a healthcare provider. During this time, mothers will receive information about the problem of premature adolescent sexual activity, support in preventing or reducing their children's sexual risk behavior, instruction about how to talk with their children about sexual risk behavior, and targeted homework activities. The healthcare provider will endorse the intervention separately for mothers and adolescents. All parents will also receive one follow-up phone call to increase the probability that the homework tasks will be completed.
Participants in this study will also be assigned to one of the following three groups: an experimental group; an active control group; or a passive control group. Participants in all groups will complete three questionnaires over the course of the study to assess outcomes. Participants in the experimental and active control groups will partake in an intervention session with a provider extender. Parents in the experimental group will meet with the provider extender to discuss effective parent-adolescent communication strategies. They will also receive take-home materials to help them communicate with and parent their adolescents to reduce sexual risk behavior. Parents in the active control group will meet with the provider extender to discuss adolescent nutrition and receive informational brochures.
One booster session will take place via telephone for parents in the experimental and active control groups. The booster call will occur approximately 1 month after study entry. No such booster calls will be provided to parents in the passive control condition.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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New York
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New York, New York, Stati Uniti, 10003
- New York University
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Adolescents must be between the ages of 11 and 14 years old
- Adolescent is able to agree to being a participant
- Participant must be able to participate in questionnaire and intervention activities
- Participant must be of Latino or African American descent
Exclusion Criteria:
- Any cognitive or psychiatric disability that would prevent successful participation in questionnaire or intervention activities
Piano di studio
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: Sex Education + Standard Care
Participating mothers will receive sex education information while their child is having a physical exam.
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The intervention will take place in a pediatric health care clinic and will be coordinated through provider extenders when healthcare providers see youth fora non-acute care visit.
A mother of the adolescent will meet with a provider extender for approximately 30 minutes while her child is being examined by a healthcare provider.
During this time, the intervention will be delivered to the mother.
At the conclusion of the session, the mother will be given reference materials to take home and tasks to perform to facilitate discussions about sex with her adolescent.
The healthcare provider will endorse the intervention separately for mothers and adolescents.
There will be one follow-up booster session administered through phone calls to increase completion probabilities of the tasks.
The target behavior is sexual activity in adolescents.
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Comparatore attivo: Hygiene & Nutrition Education + Standard Care
Participating mothers will receive information on hygiene and nutrition while their child is having a physical exam.
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The active control group will take place in a pediatric health care clinic and will be coordinated through provider extenders when healthcare providers see youth for a non-acute care visit.
The mother of the adolescent will meet with a provider extender for approximately 30 minutes while her child is being examined by a healthcare provider.
During this time, the active control on hygiene and nutrition will be delivered to the mother.
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Nessun intervento: No Education + Standard Care
Participating mothers who are passive controls will not receive any additional information while their child is having a physical exam.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Incidence of vaginal intercourse
Lasso di tempo: Measured at 12 months post-intervention
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Measured at 12 months post-intervention
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Incidence of condom use
Lasso di tempo: Measured at 12-months post-intervention
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Measured at 12-months post-intervention
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Number of sexual partners
Lasso di tempo: Measured at 12 months post-intervention
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Measured at 12 months post-intervention
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|
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Behavioral intentions
Lasso di tempo: Measured at 12 months post-intervention
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Behavioral intentions to engage in sexual intercourse will be assessed based on responses to three statements, each using a five point agree-disagree scale.
The items are: (a) I think I am ready to have sexual intercourse; (b) I would have sexual intercourse now if I had a boy who would do it with me; and (c) I plan on having sexual intercourse in the next six months.
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Measured at 12 months post-intervention
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Incidence of vaginal intercourse
Lasso di tempo: Measured at 3 months post-intervention
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Measured at 3 months post-intervention
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Incidence of condom use
Lasso di tempo: Measured at 3 months post-intervention
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Measured at 3 months post-intervention
|
|
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Number of sexual partners
Lasso di tempo: Measured at 3 months post-intervention
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Measured at 3 months post-intervention
|
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Behavioral intentions
Lasso di tempo: Measured at 3 months post-intervention
|
Behavioral intentions to engage in sexual intercourse will be assessed based on responses to three statements, each using a five point agree-disagree scale.
The items are: (a) I think I am ready to have sexual intercourse; (b) I would have sexual intercourse now if I had a boy who would do it with me; and (c) I plan on having sexual intercourse in the next six months.
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Measured at 3 months post-intervention
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Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Vincent Guilamo-Ramos, PhD, ANP-BC, New York University
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- NIH_066159
- R01HD066159 (Sovvenzione/contratto NIH degli Stati Uniti)
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