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Theory of Planned Behavior-Based Digital Addiction and Screen Time Management Training for Teachers

18 de junho de 2026 atualizado por: Belkıs CAN, Aydin Adnan Menderes University

The Impact of a Planned Behavior Theory-Based Digital Addiction and Screen Time Management Training on Teachers' Internet Addiction, Sleep Quality, and Psychological Well-being

This thesis focuses on problematic internet use, a widespread issue in contemporary society, and its negative effects on sleep quality and psychological well-being. The indispensable role of the internet in daily life and the risks associated with excessive use constitute an important area of research, particularly in relation to internalizing symptoms and health-related problems. Within this context, considering teachers' intensive engagement with digital media and their role as role models, the study aims to improve their awareness and behaviors regarding digital media use.

The aim of the thesis is to examine the effects of a Theory of Planned Behavior (TPB)-based Digital Addiction and Screen Time Management training program on levels of internet addiction, sleep quality, and psychological well-being among middle school teachers in Aydın province, using a randomized controlled experimental design.

In terms of methodology, a total of 102 teachers-51 in the intervention group and 51 in the control group-will be assessed before and after the training. Data will be collected using a Personal Information Form, the Young Internet Addiction Test-Short Form, the Pittsburgh Sleep Quality Index, and the Psychological Well-Being Scale.

The expected outcomes are that the implemented training will significantly reduce teachers' levels of internet addiction, improve their sleep quality, and lead to improvements in psychological well-being. These findings are expected to contribute to teachers' health and to provide guidance for the development of similar intervention programs for other populations.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

80

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

    • Aydın
      • Efeler, Aydın, Turquia (Türkiye)
        • AydınAdnan Menderes University, Faculy of Nursing, Division Public Health Nursing

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

  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Teachers who voluntarily agree to participate in the study and provide written informed consent.

    • Teachers who regularly use digital devices and the internet in their daily lives.

Exclusion Criteria:

  • Teachers who are receiving medical treatment or psychological support due to digital addiction, sleep disorders, or psychological conditions.
  • Teachers who are unable to attend the training program on a regular basis.

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: Pesquisa de serviços de saúde
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: experimental group
The teachers in the experimental group were provided with Digital Addiction and Screen Time Management Trainings based on the Theory of Planned Behavior, which were developed by the researchers through literature review and expert opinions.
The Digital Addiction and Screen Time Management Training Based on the Theory of Planned Behavior was implemented over a period of six weeks.
Experimental: Control group
The control group received no intervention.
The control group received no intervention.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Personal Information Form
Prazo: Baseline, immediately after intervention, 3 month after intervention.
The form, prepared by the researchers, consists of 9 questions created in line with the literature review, covering general information about the teachers' socio-demographic characteristics.
Baseline, immediately after intervention, 3 month after intervention.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Young Internet Addiction Test-Short Form
Prazo: Baseline, immediately after intervention, 3 month after intervention.
The scale was originally developed by Young, and its short form was later created by Pawlikowski, Altstötter-Gleich, and Brand. The scale is a 12-item, unidimensional, 5-point Likert-type scale (scored from 1 to 5). The Turkish adaptation of the scale was carried out by Kutlu and colleagues. The total score ranges from 12 to 60, with no reverse-coded items or cut-off point. Higher scores on the scale indicate a higher level of internet addiction in the individual. While the Cronbach's Alpha internal consistency coefficient of the YIAT-SF scale was 0.85, this value was calculated as 0.89 in this study.
Baseline, immediately after intervention, 3 month after intervention.

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Pittsburgh Sleep Quality Index (PSQI)
Prazo: Baseline, immediately after intervention, 3 month after intervention.
Developed by Buysse et al. (1989), PSQI measures sleep quality/problems over the past month. Cronbach's alpha = 0.80; validity confirmed via test-retest. Turkish adaptation by Ağargün et al. (1996) also showed α = 0.80, confirming psychometric stability. Total 24 items: 19 self-reported, 5 based on spouse/roommate observations (clinical use only; roommate item excluded from scoring). Scoring uses 18 items across 7 components, each item 0-3. Total score 0-21; ≥5 = clinically significant. Components: Subjective Sleep Quality (item 6), Sleep Latency (items 2+5a), Sleep Duration (item 4), Sleep Efficiency (items 1+3+4), Sleep Disturbances (5b-5j), Medication Use (item 7), Daytime Dysfunction (items 8+9). Item 4 is used for both Sleep Duration and Sleep Efficiency, a key design feature.
Baseline, immediately after intervention, 3 month after intervention.
Psychological Well-Being Scale
Prazo: Baseline, immediately after intervention, 3 month after intervention.
Diener and colleagues (2009) developed a measurement tool to assess individuals' socio-psychological health status (Diener et al., 2010). This scale was later adapted to Turkish culture by Telef (2013) and transformed into an 8-item form (Telef et al., 2013). In the analyses conducted, the factor loadings of the scale items were found to range between 0.54 and 0.76. As a result of the reliability analyses of the scale, the Cronbach's alpha coefficient was calculated as 0.80. It was determined that the item-total correlation coefficients ranged between 0.41 and 0.63, and the t-test results were statistically significant (p < 0.001). The response options used in the scale have a seven-point Likert-type structure: "Strongly disagree," "Disagree," "Slightly disagree," "Undecided," "Slightly agree," "Agree," and "Strongly agree.
Baseline, immediately after intervention, 3 month after intervention.

Colaboradores e Investigadores

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

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)

8 de outubro de 2025

Conclusão Primária (Real)

25 de dezembro de 2025

Conclusão do estudo (Real)

19 de março de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

11 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

16 de junho de 2026

Primeira postagem (Real)

18 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

18 de junho de 2026

Última verificação

1 de junho 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

The data sets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

Prazo de Compartilhamento de IPD

6 months after publication

Critérios de acesso de compartilhamento IPD

Relevance to the topic of the study and approval of all co-authors within 1 month of receiving the request.

Tipo de informação de suporte de compartilhamento de IPD

  • 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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