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Avaliação da Linha de Apoio WhatsOK para Jovens com Preocupações sobre Pensamentos e Comportamentos Sexuais

1 de outubro de 2026 atualizado por: Center for Violence Prevention Research Inc

Uma Avaliação de Ensaio Controlado Randomizado do WhatsOK para a Prevenção Primária de Comportamentos Sexuais Problemáticos em Jovens

Research suggests up to 77% of harmful sexual experiences during childhood are caused by other youth. Sometimes called peer-peer abuse or youth-perpetrated child sexual abuse, problematic and harmful sexual behavior among youth (PHSBY) involves sexual behaviors that are not developmentally appropriate and have potential to cause harm to the child or children involved.

Compared to adults, children and adolescents who engage in sexual exploration are at greater risk of making mistakes or causing harm, in large part because they have insufficient information about healthy sexual behavior and development, consent, and related concepts. However, the available support, information, and resources for youth who have engaged in or are at risk of engaging in PSHB are limited.

To address these unmet needs, Stop it Now! (stopitnow.org) created the first youth-focused website and helpline services (WhatsOK) for young people with concerns about their sexual thoughts, interests, and behaviors. WhatsOK.org is a microsite developed specifically for youth aged 14-21 years. If a child or young person has concerns about their sexual thoughts or behaviors, the WhatsOK Online Help Center and Helpline can provide support and resources to support healthy behavior and prevent problematic or harmful behavior. If someone has already engaged in PHSBY or if they are unsure about whether what has been done is illegal, they can still reach out for confidential help to learn about taking steps to stop.

Preliminary findings from a longitudinal, observational study of the WhatsOK helpline suggest that youth are willing to seek out help for their (and others') sexual interests and behaviors, highlighting the critical need for prevention strategies targeting youth with potentially concerning sexual behaviors. We examined the characteristics of contacts to the WhatsOK helpline via data collected from pre-set questions on age, primary reason for contact, timing of inquiry relative to other help-seeking, and timing relative to harm caused. Most inquiries came from youth aged 14 to 21 (57.7%) via email (54.4%). Over half (54.6%) had already engaged in harmful or illegal behaviors or were potentially at risk to do so. The majority of contacts sought help prior to seeking out other external professional resources (54%).

The current study is a randomized control trial evaluating the impact of the WhatsOK helpline in reducing PHSBY and improving help-seeking attitudes and behavior in a sample of participants ages 14-17 with concerns about their sexual thoughts and behaviors.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

920

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

    • Florida
      • Jacksonville, Florida, Estados Unidos, 32235
        • Recrutamento
        • Center for Violence Prevention Research
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

14 anos a 17 anos (Filho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • must be ages 14-17 years at baseline
  • must have concerns about their sexual thoughts or behaviors
  • must be able to read, write, and speak in English

Exclusion Criteria:

  • Under 14 or over 17 years of age
  • Does not have concerns about their sexual thoughts or behaviors
  • Previously contacted a helpline or hotline for concerns about their sexual thoughts or behaviors
  • Is not able to read, write, or speak in English
  • Does not consent to participate

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Helpline condition

Participants will be directed to the WhatsOK helpline

Participants will be directed to contact the WhatsOK helpline, where they can confidentially discuss their concerns about sexual thoughts or behaviors with a trained counselor

Sem intervenção: Control condition

Participants will complete all follow-up surveys but not be directed to the helpline

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Help-seeking behaviors
Prazo: Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Investigators will measure whether participants have sought support (beyond their assigned treatment condition) for concerns about their sexual thoughts and behaviors.

Help-seeking behaviors will be measured using two items. 1.) [In the past time], have you tried to find information related to concerns about your sexual thoughts, feelings, or behaviors? and 2.) [In the past time], have you reached out for support about concerns related to your sexual thoughts, feelings, or behaviors?

Response options are binary "yes/no". Participants can also select "prefer not to answer".

Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)
Sexual behaviors
Prazo: Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Investigators will measure a variety of sexual behaviors, such as engaging in sexual contact with someone who does not consent (e.g, Have you ever made someone do sexual things when they didn't want to?); engaging in sexual contact with a young child; viewing or sharing sexual images of/with someone who does not consent; viewing, sharing, or creating sexual images of someone under the age of 18. Researcher created measure.

Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Safety Planning
Prazo: Participants' mental health will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Participants will be asked two questions about safety planning behaviors that ask if participants have ever thought about specific ways or taken specific steps to make sure they don't engage in sexual behaviors that are illegal or could harm someone else. Participants are asked to choose the statement that best describes them. Options include: "yes, I have thought of specific ways/taken specific steps to avoid these behaviors", "no -I know I won't engage in these behaviors", "no - I need more information to come up with specific ways" or "no - I have ideas but haven't been able to put them into action yet", "no - avoiding these behaviors is not a priority for me". "something else" and "prefer not to answer".

Participants' mental health will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)
Well-being
Prazo: Participants' mental health will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Well-being will be assessed using the 7-item Students' Life Satisfaction Scale. A 7-point Likert scale (from very strongly disagree to very strongly agree) will be used to measure participants' responses. Participants are also able to select "prefer not to answer".

Participants' mental health will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)
Internal shame
Prazo: Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Investigators will measure internal shame using the 4-item Internal Shame Subscale of the External and Internal Shame Scale. Responses are measures using a 7-point Likert scale ranging from "very strongly disagree" to "very strongly agree". Participants can also select "prefer not to answer".

Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)
Perceived resources
Prazo: Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Investigators will measure participants perceptions of resources in their lives for concerns about sexual thoughts and behaviors through a 4-item researcher-created scale (e.g., "There are safe resources available to help people my age with similar concerns about their sexual thoughts, feelings, or behaviors"). Responses are measured through a 7-point Likert scale that ranges from "very strongly disagree" to "very strongly agree". Participants are also able to select "prefer not to answer".

Participants' behaviors will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)
Perceived self-efficacy
Prazo: Participants' perceived self-efficacy will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

This is a researcher-created scale. This scale consists of 4 items to measure participants' perceived ability to avoid engaging in harmful or illegal behaviors (e.g., "If I have sexual thoughts that make me feel worried or concerned, I can take steps to address them."). Items are scored on a 7-point Likert Scale which ranges from "very strongly disagree" to "very strongly agree"). Participants are also able to select "prefer not to answer".

Participants' perceived self-efficacy will be measured at baseline, t2 (baseline + 3 days), T3 (baseline + 14 days), T4 (baseline + 45 days), and T5 (baseline + 90 days)

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Publicações e links úteis

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Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

6 de abril de 2026

Conclusão Primária (Estimado)

29 de setembro de 2028

Conclusão do estudo (Estimado)

29 de setembro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

19 de fevereiro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

7 de abril de 2026

Primeira postagem (Real)

13 de abril de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de outubro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de outubro de 2026

Última verificação

1 de outubro de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • CE-25-026
  • 1 U01CE003741-01-00 (Número de outro subsídio/financiamento: Centers for Disease Control and Prevention)
  • 1U01CE003741-01 (Concessão/Contrato do NIH dos EUA)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Descrição do plano IPD

Data sharing would require a data use agreement. Data will be collected on sensitive information (e.g., potentially harmful behaviors) and thus would not be appropriate to release without restrictions.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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