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Ensaio de Otimização Fatorial para Testar os Efeitos dos Componentes de Intervenção de Enfrentamento

4 de setembro de 2026 atualizado por: Karey O'Hara, Arizona State University

Promovendo enfrentamento eficaz por crianças expostas a conflitos interparentais pós-divórcio para reduzir o risco de problemas de saúde mental

This study will identify components for inclusion in a coping intervention package to reduce mental health problems among children exposed to high interparental conflict after parental separation/divorce. Reappraisal, distraction, and relaxation coping strategies are related to fewer mental health problems among children, making intervention components based on these strategies key candidates for inclusion in an optimized coping intervention. The primary aim is to experimentally assess the main and interactive effects of three digital intervention coping components (reappraisal, distraction, relaxation) on children's coping efficacy, emotional security, and internalizing and externalizing problems. Secondary aims are to assess indirect effects of the intervention components on children's coping efficacy, emotional security, and internalizing and externalizing problems through their cognitive, emotional, and behavioral reactions to post-separation/divorce interparental conflict events.

Visão geral do estudo

Descrição detalhada

A randomized and counterbalanced 2x2x2 factorial trial (N = 144 children, ages 9-12) will be conducted to assess the individual effects of the three digital coping intervention components. The three components to be tested will be: (1) Reappraisal (No vs. Yes), (2) Distraction (No vs. Yes), (3) Relaxation (No vs. Yes). Components that meet a priori thresholds for meaningful change will be combined to form an intervention package that will be evaluated in a subsequent randomized controlled trial.

Tipo de estudo

Intervencional

Inscrição (Real)

148

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.

Locais de estudo

    • Arizona
      • Tempe, Arizona, Estados Unidos, 85087
        • Arizona State University

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

9 anos a 12 anos (Filho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • child between ages 9-12 whose parents are separated or divorced
  • child and one parent are fluent in English
  • a parent with sufficient contact (i.e., at least 4 overnights and/or 12 daytime visits per month) with child who is willing to complete study assessments and has legal right to give permission for the child to participate in research
  • child-report of high exposure to IPC (mean Z score ≥ 40th percentile on the two child report measures of IPC; score standardization based on data from 559 youth whose parents participated in an experimental parenting program)
  • elevated internalizing or externalizing problems (T score in the borderline clinical range according to either child or parent report on the BPM).

Exclusion Criteria:

  • in active therapy
  • score ≥ 99th percentile on either internalizing and externalizing problems subscale
  • endorse suicidality (will be ineligible for the study and referred for treatment)

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 fatorial
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Education

Participants will complete an educational digital module and no skills-based digital modules.

This is a constant component; all participants will get a psychoeducation digital module.

Experimental: Education + Reappraisal

Participants will complete an educational digital module and a skills-based digital module that teaches reappraisal coping.

This is a constant component; all participants will get a psychoeducation digital module.

This digital module will teach reappraisal coping skills.

Experimental: Education + Distraction

Participants will complete an educational digital module and a skills-based digital module that teaches distraction coping.

This is a constant component; all participants will get a psychoeducation digital module.

This digital module will teach distraction coping skills.

Experimental: Education + Relaxation

Participants will complete an educational digital module and a skills-based digital module that teaches relaxation coping.

This is a constant component; all participants will get a psychoeducation digital module.

This digital module will teach relaxation coping skills.

Experimental: Education + Reappraisal + Distraction

Participants will complete an educational digital module and two skills-based digital modules, one that teaches reappraisal coping and one that teaches distraction coping.

This is a constant component; all participants will get a psychoeducation digital module.

This digital module will teach reappraisal coping skills.

This digital module will teach distraction coping skills.

Experimental: Education + Reappraisal + Relaxation

Participants will complete an educational digital module and two skills-based digital modules, one that teaches reappraisal coping and one that teaches relaxation coping.

This is a constant component; all participants will get a psychoeducation digital module.

This digital module will teach reappraisal coping skills.

This digital module will teach relaxation coping skills.

Experimental: Education + Distraction + Relaxation

Participants will complete an educational digital module and two skills-based digital modules, one that teaches distraction coping and one that teaches relaxation coping.

This is a constant component; all participants will get a psychoeducation digital module.

This digital module will teach distraction coping skills.

This digital module will teach relaxation coping skills.

Experimental: Education + Reappraisal + Distraction + Relaxation

Participants will complete an educational digital module and three skills-based digital modules, one that teaches reappraisal coping, one that teaches distraction coping, and one that teaches relaxation coping.

This is a constant component; all participants will get a psychoeducation digital module.

This digital module will teach reappraisal coping skills.

This digital module will teach distraction coping skills.

This digital module will teach relaxation coping skills.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Mean Child-Reported Interparental Emotional Security Score on the SIS-SF at 3-Month Follow-Up
Prazo: approximately 3 months after posttest

Child-reported Security in the Interparental Subsystem Scale-Short Form (SIS-SF; Holt et al., 2020). The score is the mean of 17 items rated from 0 (not at all true) to 3 (very true for me). Higher scores indicate greater interparental emotional security (better outcome). The outcome table reports observed scores; factorial analyses adjust for baseline SIS-SF and prespecified covariates.

approximately 3 months after posttest
Mean Child-Reported Family Emotional Security Score on the SIFS at 3-Month Follow-Up
Prazo: approximately 3 months after posttest

Child-reported Security in the Family System Scale (SIFS; Forman & Davies, 2005). The score is the mean of 24 items rated from 0 (completely disagree) to 3 (completely agree). Higher scores indicate greater family emotional security (better outcome). The outcome table reports observed scores; the attached factorial analyses adjust for the baseline SIFS score and prespecified covariates.

approximately 3 months after posttest
Mean Child-Reported Coping Efficacy Score on the CES at 3-Month Follow-Up
Prazo: approximately 3 months after posttest

Child-reported Coping Efficacy Scale (CES; Sandler et al., 2000). The score is the mean of 7 items rated from 0 (not at all) to 3 (very). Higher scores indicate greater coping efficacy (better outcome). The outcome table reports observed scores; the attached factorial analyses adjust for the baseline CES score and prespecified covariates.

approximately 3 months after posttest
Mean Child-Reported Internalizing Problems Score on the BPM at 3-Month Follow-Up
Prazo: approximately 3 months after posttest

Child-reported Brief Problem Monitor (BPM) Internalizing Problems scale. The score is the mean of 6 items rated from 0 (not true) to 2 (very true). Higher scores indicate more internalizing problems (worse outcome). The outcome table reports observed scores; the attached factorial analyses adjust for the baseline child-reported BPM Internalizing Problems score and prespecified covariates.

approximately 3 months after posttest
Mean Parent-Reported Internalizing Problems Score on the BPM at 3-Month Follow-Up
Prazo: approximately 3 months after posttest

Parent-reported Brief Problem Monitor (BPM) Internalizing Problems scale. The score is the mean of 6 items rated from 0 (not true) to 2 (very true). Higher scores indicate more internalizing problems (worse outcome). The outcome table reports observed scores; the attached factorial analyses adjust for the baseline parent-reported BPM Internalizing Problems score and prespecified covariates.

approximately 3 months after posttest
Mean Child-Reported Externalizing Problems Score on the BPM at 3-Month Follow-Up
Prazo: approximately 3 months after posttest

Child-reported Brief Problem Monitor (BPM) Externalizing Problems scale. The score is the mean of 7 items rated from 0 (not true) to 2 (very true). Higher scores indicate more externalizing problems (worse outcome). The outcome table reports observed scores; the attached factorial analyses adjust for the baseline child-reported BPM Externalizing Problems score and prespecified covariates.

approximately 3 months after posttest
Mean Parent-Reported Externalizing Problems Score on the BPM at 3-Month Follow-Up
Prazo: approximately 3 months after posttest

Parent-reported Brief Problem Monitor (BPM) Externalizing Problems scale. The score is the mean of 7 items rated from 0 (not true) to 2 (very true). Higher scores indicate more externalizing problems (worse outcome). The outcome table reports observed scores; the attached factorial analyses adjust for the baseline parent-reported BPM Externalizing Problems score and prespecified covariates.

approximately 3 months after posttest

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Karey L O'Hara, PhD, Arizona State University

Publicações e links úteis

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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)

18 de fevereiro de 2023

Conclusão Primária (Real)

30 de março de 2026

Conclusão do estudo (Real)

30 de março de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

17 de fevereiro de 2023

Enviado pela primeira vez que atendeu aos critérios de CQ

8 de abril de 2023

Primeira postagem (Real)

21 de abril de 2023

Atualizações de registro de estudo

Última Atualização Postada (Real)

30 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

4 de setembro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

Study results will be shared through presentations at conferences and submissions in peer-reviewed journals. In addition, after taking all steps necessary to minimize possible re-identification of confidential data, I will make data, codebooks, and analysis scripts available to appropriate parties to verify findings and conclusions.

Prazo de Compartilhamento de IPD

one year post data collection

Critérios de acesso de compartilhamento IPD

qualified researchers who have gained IRB approval and pre-registered their analyses

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF
  • ANALYTIC_CODE
  • CSR

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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