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The Impact of the Objective Structured Clinical Examination (OSCE)

17 juin 2026 mis à jour par: Elif Çoban, Kırıkkale University

The Impact of OSCE on Clinical Competence, Anxiety, and Educational Satisfaction in Dental Students

This study aims to compare two different educational and assessment approaches used for teaching pre-extraction clinical evaluation skills to undergraduate dental students. Before performing a simple tooth extraction, students are expected to obtain a medical history, identify systemic risk factors, determine extraction indications, communicate effectively with patients, and make appropriate clinical decisions.

Participants will be assigned to either an Objective Structured Clinical Examination (OSCE)-based educational approach or a traditional teaching and assessment approach. Students' clinical performance, communication skills, clinical reasoning abilities, learning satisfaction, self-confidence, and examination-related anxiety will be evaluated and compared between groups.

The findings of this study are expected to provide evidence regarding the effectiveness of OSCE in undergraduate dental education and contribute to the development of more effective training and assessment strategies for clinical competency acquisition.

Aperçu de l'étude

Description détaillée

Simple tooth extraction is one of the most frequently performed procedures in dental practice. Although the technical aspects of extraction are important, successful patient management requires accurate medical history taking, identification of systemic risk factors, appropriate treatment planning, clinical decision-making, and effective communication with patients. Deficiencies in these competencies may adversely affect patient safety and treatment outcomes.

Traditional educational approaches in dental schools primarily focus on theoretical knowledge and may not adequately provide opportunities for students to demonstrate and apply their knowledge in realistic clinical scenarios. Consequently, variations may occur among students regarding diagnostic reasoning, risk assessment, communication skills, and clinical decision-making.

The Objective Structured Clinical Examination (OSCE) is a structured and standardized assessment method widely used in health professions education. OSCE enables students to demonstrate clinical competencies through scenario-based stations that simulate real-life patient encounters. Previous studies have shown that OSCE can improve students' clinical performance, decision-making abilities, and educational satisfaction while providing a more objective assessment of clinical competence. However, concerns regarding examination-related anxiety and the resource-intensive nature of OSCE remain subjects of ongoing investigation.

The present study aims to compare an OSCE-based educational and assessment model with a traditional teaching and assessment approach in the context of pre-extraction clinical evaluation. The educational content focuses on competencies required before performing a simple tooth extraction, including patient history taking, identification of systemic conditions that may affect treatment, determination of extraction indications, patient communication, informed consent procedures, and clinical reasoning.

Students participating in the study will receive training according to their assigned educational method. Following the educational intervention, participants will be evaluated using standardized assessment tools. Primary outcomes will include measures of clinical competency and performance related to pre-extraction patient evaluation. Secondary outcomes will include learning satisfaction, self-confidence in learning, and examination-related anxiety.

By examining both educational effectiveness and learner perceptions, this study seeks to determine whether OSCE-based training offers advantages over traditional educational approaches in developing clinical competencies required for safe and effective dental practice. The findings may contribute to evidence-based improvements in undergraduate dental curricula and provide additional data regarding the implementation of OSCE in dental education programs.

Type d'étude

Observationnel

Inscription (Réel)

104

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Yahşihan
      • Kirikkale, Yahşihan, Turquie (Türkiye), 71450
        • Kırıkkale University Faculty of Dentistry

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant

Accepte les volontaires sains

Oui

Méthode d'échantillonnage

Échantillon de probabilité

Population étudiée

This study was conducted as a prospective randomized controlled study to evaluate the skills of 4th-year students at Faculty of Dentistry regarding a clinical case with an indication for simple tooth extraction. The study population consisted of 4th-year students at Faculty of Dentistry who had received theoretical and practical training on tooth extraction within the scope of the Oral and Maxillofacial Surgery course.

La description

Inclusion Criteria:

  • Fourth-year student enrolled in the Faculty of Dentistry.
  • Completion of theoretical and practical training in tooth extraction.
  • Age 18-25 years.
  • Voluntary agreement to participate and provision of informed consent.

Exclusion Criteria:

  • Enrollment in an academic year other than the fourth year or at another university.
  • Refusal to participate or withdrawal of informed consent.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
Group 1
Students assessed in the OSCE laboratory
Group 2
Students assessed using the traditional method

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Primary Outcome Measure
Délai: 1. day

Title: Clinical performance score

Description:

Clinical performance will be evaluated immediately after the assessment using the Global Rating Scale (GRS). The GRS assesses history taking, risk assessment, clinical reasoning, decision-making, patient communication, and overall clinical competence. Scores range from 1 to 5 for each domain, with higher scores indicating better clinical performance.

Time Frame:

Immediately after assessment (Day 1)

1. day
State anxiety level
Délai: Immediately before and immediately after assessment (Day 1)
State anxiety will be measured before and after the assessment using the State-Trait Anxiety Inventory - State Form (STAI-I). Total scores range from 20 to 80, with higher scores indicating greater state anxiety.
Immediately before and immediately after assessment (Day 1)
Student satisfaction and self-confidence in learning
Délai: Immediately after the educational intervention (Day 1)
Student satisfaction and self-confidence in learning will be evaluated immediately after the educational intervention using the Turkish version of the 12-item Student Satisfaction and Self-Confidence in Learning Scale. The scale consists of 12 items rated on a 5-point Likert scale, with total scores ranging from 12 to 60. Higher scores indicate greater student satisfaction and self-confidence in learning.
Immediately after the educational intervention (Day 1)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Secondary Outcome Measure
Délai: 2 weeks after the educational intervention
Knowledge retention will be assessed 2 weeks after the educational intervention using the Global Rating Scale (GRS). Students will evaluate a standardized clinical case similar to that used during training. The GRS rates each domain on a 5-point scale (1 = lowest performance, 5 = highest performance). Higher scores indicate better knowledge retention.
2 weeks after the educational intervention

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

20 février 2026

Achèvement primaire (Réel)

1 avril 2026

Achèvement de l'étude (Réel)

4 mai 2026

Dates d'inscription aux études

Première soumission

12 juin 2026

Première soumission répondant aux critères de contrôle qualité

17 juin 2026

Première publication (Réel)

24 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

24 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

17 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • Decision No: 2026.02.04

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

De-identified individual participant data, including demographic characteristics, Global Rating Scale (GRS) scores, State-Trait Anxiety Inventory (STAI-I) scores, Student Satisfaction and Self-Confidence in Learning Scale scores, and knowledge retention assessment results, will be available upon reasonable request to the corresponding author following publication of the study results.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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