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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07804108
Effect of Mosaic Art on Episiotomy Repair Skills, Anxiety, and Learning Attitudes in Midwifery Students (MOSAIC-EPI)
31 de agosto de 2026 actualizado por: Mine Gokduman Keles, Kahramanmaras Sutcu Imam University
The Effect of Mosaic Art Practice on Fine Motor Skills, Anxiety Levels, and Learning Attitudes in Episiotomy Repair Among Midwifery Students: A Randomized Controlled Trial
Objective: The aim of this study is to evaluate the effect of mosaic art in midwifery education on episiotomy repair performance, self-efficacy, and anxiety: a randomized controlled trial.
Method/Data Collection Techniques: The study was planned in a two-parallel-group randomized controlled experimental design including pre-test and post-test measurements.
The study will be conducted with third-year students studying in the Midwifery Department of the Faculty of Health Sciences at Kahramanmaraş Sütçü İmam University during the fall semester of the 2026-2027 academic year.
The sample size was calculated using the G*Power 3.1.9.7 program, and based on Cohen's effect size d=0.55,
α=0.05, and 80% power, a total of 106 students were planned to be included in the study, with 53 students in each group.
Participants will be assigned to intervention and control groups using a simple randomization method.
The intervention group will receive structured mosaic art training for six weeks, with two sessions per week, while the control group will not receive any art-based application during this period.
Following the intervention, both groups will receive theoretical and practical training in standard episiotomy repair.
Data will be collected using the Participant Information Form, State Anxiety Scale (STAI-TX I), Episiotomy Self-Efficacy Scale, Attitudes Towards Learning Scale, and Episiotomy Repair Skill Assessment Form.
Appropriate descriptive statistics and parametric or non-parametric comparison tests will be used in the analysis of the data, with a statistical significance level of p<0.05.
Expected Results: This research is expected to provide scientific evidence regarding the use of art-based teaching methods in midwifery education by revealing the effect of mosaic art application on midwifery students' episiotomy repair skills, self-efficacy, attitudes towards learning, and state anxiety levels.
It is anticipated that the research results will contribute to the development of effective teaching strategies in psychomotor skills training and the strengthening of midwifery education programs.
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
106
Fase
- No aplica
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
Acepta Voluntarios Saludables
Sí
Descripción
Inclusion Criteria:
- Being enrolled as a third-year student in the Department of Midwifery, Faculty of -Health Sciences, Kahramanmaraş Sütçü İmam University, during the Fall -semester of the 2026-2027 academic year.
- Volunteering to participate in the study.
- Providing written informed consent.
- Having no previous clinical practice experience in episiotomy repair.
- Having no previous participation in a structured training program involving mosaic art or similar activities requiring fine motor skills.
Exclusion Criteria:
- Having previous clinical practice experience in episiotomy repair.
- Having previously participated in a structured mosaic art training program or a similar structured program requiring fine motor skills.
- Having a condition that prevents participation in the mosaic art activities or episiotomy repair simulation practice.
- Declining or withdrawing consent to participate in the study
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: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Mosaic Art Group
Participants in this group will receive the planned mosaic art intervention before episiotomy repair training.
The mosaic art program will be conducted for 6 weeks, with two 45-minute sessions per week.
Following the intervention, participants will receive the standard theoretical and practical episiotomy repair training.
|
Participants assigned to the intervention group will participate in a structured mosaic art program for six weeks before episiotomy repair training.
The program will consist of two 45-minute sessions per week (12 sessions in total).
Participants will engage in mosaic art activities requiring coordinated hand and finger movements and fine motor control.
After completion of the mosaic art program, participants will receive the same theoretical and practical episiotomy repair training provided to the control group.
Participants will receive standardized theoretical and practical episiotomy repair training.
The training will include 2 hours of theoretical instruction and 6 hours of practical training using a silicone episiotomy repair model.
The same standardized episiotomy repair training will be provided to participants in both study groups.
|
|
Comparador activo: Control Group
Participants in the control group will not receive the mosaic art intervention.
They will receive the same standard theoretical and practical episiotomy repair training as the intervention group
|
Participants will receive standardized theoretical and practical episiotomy repair training.
The training will include 2 hours of theoretical instruction and 6 hours of practical training using a silicone episiotomy repair model.
The same standardized episiotomy repair training will be provided to participants in both study groups.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Episiotomy Self-Efficacy
Periodo de tiempo: Immediately before and immediately after the episiotomy repair training
|
Episiotomy self-efficacy will be assessed using the Episiotomy Self-Efficacy Scale developed by Yolcu et al. (2025).
The scale consists of 17 items across four subdimensions: cognitive (5 items), affective (5 items), motivation (3 items), and psychomotor (4 items).
Each item is rated on a 5-point Likert scale ranging from 1 (Strongly Disagree) to 5 (Strongly Agree).
There are no reverse-scored items.
The total score ranges from 17 to 85, with higher scores indicating greater episiotomy self-efficacy.
|
Immediately before and immediately after the episiotomy repair training
|
|
Episiotomy Repair Skill Performance
Periodo de tiempo: Baseline and immediately post-intervention
|
Episiotomy repair skill performance will be assessed using the Episiotomy Repair Skill Assessment Form developed by the researchers based on the relevant literature and expert review.
The form consists of 20 procedural steps assessing the performance of
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Baseline and immediately post-intervention
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
State Anxiety (STAI Form TX-I)
Periodo de tiempo: Baseline and immediately post-intervention
|
State anxiety will be assessed using the State-Trait Anxiety Inventory, State Anxiety Form (STAI Form TX-I).
The scale consists of 20 items rated on a 4-point scale.
Total scores range from 20 to 80, with higher scores indicating higher levels of state anxiety.
|
Baseline and immediately post-intervention
|
|
Attitudes Toward Learning
Periodo de tiempo: Baseline and immediately post-intervention
|
Attitudes toward learning will be assessed using the Attitudes Toward Learning Scale developed by Kara (2010).
The scale consists of 40 items and four subdimensions: Nature of Learning (7 items), Anxiety About Learning (13 items), Expectations About Learning (9 items), and Openness to Learning (11 items).
Items are rated on a 5-point Likert scale from 1 (Strongly Disagree) to 5 (Strongly Agree).
Eleven negatively worded items are reverse scored.
Higher scores indicate more positive attitudes toward learning.
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Baseline and immediately post-intervention
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
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 (Estimado)
28 de septiembre de 2026
Finalización primaria (Estimado)
30 de diciembre de 2026
Finalización del estudio (Estimado)
30 de diciembre de 2026
Fechas de registro del estudio
Enviado por primera vez
27 de agosto de 2026
Primero enviado que cumplió con los criterios de control de calidad
31 de agosto de 2026
Publicado por primera vez (Actual)
4 de septiembre de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
4 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
31 de agosto de 2026
Última verificación
1 de agosto de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- KSÜ-MOSAIC-EPI-2026
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. .