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

28 de junio de 2026 actualizado 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.

Descripción general del estudio

Descripción detallada

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 estudio

Intervencionista

Inscripción (Actual)

56

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Ankara, Turquía (Türkiye), 06010
        • Health Sciences University Gülhane Faculty of Nursing

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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.

Sin intervención: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Internet Addiction Severity Assessed by Young Internet Addiction Test - Short Form
Periodo de tiempo: 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
Periodo de tiempo: 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

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

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

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • 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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de noviembre de 2025

Finalización primaria (Actual)

31 de enero de 2026

Finalización del estudio (Actual)

31 de enero de 2026

Fechas de registro del estudio

Enviado por primera vez

28 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

28 de junio de 2026

Publicado por primera vez (Actual)

6 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

28 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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