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Effect of Cognitive Behavioral Based Psychoeducation Program on Internet Addiction and Academic Procrastination Tendency in Nursing Students

28 de junho de 2026 atualizado por: Ümmühan Dikililer, Saglik Bilimleri Universitesi

The Effect of a Cognitive Behavioral Based Psychoeducation Program on Internet Addiction and Academic Procrastination Tendency Among Nursing Students

This randomized controlled trial was conducted to determine the effectiveness of a cognitive behavioral approach-based psychoeducation program on internet addiction and academic procrastination tendency among undergraduate nursing students.

Visão geral do estudo

Descrição detalhada

Internet addiction and academic procrastination tendency are increasingly common problems among university students and may negatively affect academic performance, psychological well-being, and professional development. Nursing students are considered a high-risk group due to intensive academic workload and frequent exposure to digital technologies. Cognitive behavioral approaches are widely used in addressing maladaptive thoughts and behaviors associated with problematic internet use and procrastination; however, evidence regarding structured psychoeducation programs based on this approach among nursing students is limited.

This randomized controlled experimental study with a pre-test, post-test, and one-month follow-up design was conducted between November 2025 and January 2026 at the Faculty of Nursing of a public university in Ankara, Türkiye. The study population consisted of undergraduate nursing students, and a total of 56 participants were included, with 28 assigned to the intervention group and 28 to the control group through random allocation.

The intervention group received a cognitive behavioral approach-based psychoeducation program consisting of eight weekly sessions. Each session lasted 90 minutes and was delivered face-to-face in a group format. For implementation purposes, the intervention group was divided into three smaller subgroups. The program focused on increasing awareness of internet use behaviors, identifying cognitive distortions, developing time management skills, and improving coping strategies. The control group did not receive any intervention during the study period.

Data were collected using a Personal Information Form, the Young Internet Addiction Test-Short Form, and the Academic Procrastination Tendency Scale. Measurements were obtained at three time points: baseline (pre-test), immediately after the intervention (post-test), and one month after the intervention (follow-up). In the control group, assessments were conducted in parallel with the intervention group.

Statistical analyses were performed using SPSS version 22.0. Normality of data distribution was assessed using the Shapiro-Wilk test. Depending on the distribution characteristics, independent samples t-test, one-way analysis of variance, Mann-Whitney U test, Friedman test, and Wilcoxon signed-rank test were used. Post-hoc analyses with Bonferroni correction were applied where appropriate. Statistical significance was set at p<0,05.

Tipo de estudo

Intervencional

Inscrição (Real)

56

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

      • Ankara, Turquia (Türkiye), 06010
        • Health Sciences University Gülhane Faculty of 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
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Aged 18 years or older
  • Being enrolled as a nursing student in a Faculty of Nursing
  • Willing to participate in the study

Exclusion Criteria:

  • Having a diagnosed psychiatric disorder
  • Being currently under psychological intervention (e.g., psychoeducation, psychotherapy) or psychiatric treatment

Participant Discontinuation Criteria (Withdrawal Criteria):

  • Incomplete or incorrectly completed data collection forms
  • Missing two consecutive intervention sessions
  • Receiving a psychiatric diagnosis during the study period

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: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Intervention Group

Participants in the intervention group received an eight-session cognitive behavioral approach-based psychoeducation program. The program was delivered face-to-face once a week in 90-minute group sessions. Participants were divided into three small subgroups for implementation.

This program was structured to enhance participants' awareness of emotions and thoughts and to develop skills in identifying and managing automatic thoughts and cognitive distortions. In addition to theoretical content, the program included practical activities based on a cognitive behavioral approach. It also incorporated relaxation exercises and training aimed at improving problem-solving and time management skills.

A structured cognitive behavioral psychoeducation program was implemented. The program focused on enhancing awareness of emotions and thoughts, identifying and managing automatic thoughts and cognitive distortions, and improving coping skills.

Each session included a brief mood check, review of the previous session, feedback on homework assignments, and structured psychoeducational activities. At the end of each session, new homework was assigned and the session was summarized.

The intervention incorporated cognitive restructuring exercises, relaxation techniques, problem-solving strategies, and time management training. The program aimed to reduce internet addiction and academic procrastination tendency among nursing students.

Sem intervenção: Control Group
Participants in the control group did not receive any intervention during the study period. Assessments were conducted at baseline, post-intervention, and one-month follow-up in parallel with the intervention group.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Internet Addiction Severity Assessed by Young Internet Addiction Test - Short Form
Prazo: Baseline, week 8 (post-intervention), and 1-month follow-up
Internet addiction severity was measured using the Young Internet Addiction Test - Short Form, a 12-item Likert-type scale. The total score ranges from 12 to 60, with higher scores indicating greater levels of internet addiction severity.
Baseline, week 8 (post-intervention), and 1-month follow-up
Academic Procrastination Tendency Assessed by Academic Procrastination Scale
Prazo: Baseline, week 8 (post-intervention), and 1-month follow-up
Academic procrastination tendency was measured using a 16-item Likert-type Academic Procrastination Scale. The total score ranges from 16 to 80, with higher scores indicating greater academic procrastination tendency.
Baseline, week 8 (post-intervention), and 1-month follow-up

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Emine Öksüz, PhD, Health Sciences University Hamidiye Faculty of Nursing, Istanbul, Turkey

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

  • Young KS; Internet addiction: the emergence of a new clinical disorder; CyberPsychology & Behavior; 1998; 1; 237-244
  • Balkıs M; Öğretmen adaylarının davranışlarındaki erteleme eğiliminin düşünme ve karar verme tarzları ile ilişkisi; Dokuz Eylül Üniversitesi; 2006; Yayınlanmamış doktora tezi
  • Aitken M E; A personality profile of the college student procrastinator; University of Pittsburgh; 1982; Dissertation Abstracts International; 43; 722
  • Kutlu M, Savci M, Demir Y, Aysan F; Young İnternet Bağımlılığı Testi Kısa Formu'nun Türkçe uyarlaması: Üniversite öğrencileri ve ergenlerde geçerlik ve güvenirlik çalışması; Anadolu Psikiyatri Dergisi; 2016; 17; 69-76
  • Pawlikowski M, Altstötter-Gleich C, Brand M; Validation and psychometric properties of a short version of Young's Internet Addiction Test; Computers in Human Behavior; 2013; 29; 1212-1223

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)

1 de novembro de 2025

Conclusão Primária (Real)

31 de janeiro de 2026

Conclusão do estudo (Real)

31 de janeiro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

28 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

28 de junho de 2026

Primeira postagem (Real)

6 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

28 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)?

NÃO

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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