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Clinical Education Environment Assessment Scale

2026年7月10日 更新者:Demet Öztürk、Lokman Hekim University

Development and Psychometric Evaluation of the Clinical Education Environment Assessment Scale for Health Sciences Students

This study aims to develop and evaluate a questionnaire that measures how health sciences students perceive the clinical environments in which they complete internships or clinical placements. The questionnaire will assess areas such as patient characteristics, supervisor support, working conditions, physical facilities, and learning experiences.

Fourth-year health sciences students who have previously completed clinical training will be invited to complete an anonymous questionnaire. Participation is voluntary, and completing the questionnaire will take approximately 10 minutes. No intervention, treatment, image recording, or biological sample collection will be involved.

The results may help universities and clinical training institutions identify strengths and areas for improvement in clinical education environments. The developed scale may also support educational quality assurance and accreditation processes.

調査の概要

状態

まだ募集していません

詳細な説明

This cross-sectional scale development study aims to develop and evaluate the psychometric properties of the Clinical Education Environment Assessment Scale for Health Sciences Students. The scale is intended to assess students' perceptions of the quality and suitability of the clinical environments in which they complete internships and clinical placements.

Clinical education is an essential component of health sciences education because it enables students to apply theoretical knowledge, develop practical skills, improve clinical decision-making, and gain experience within healthcare teams. Students' learning outcomes and satisfaction may be influenced by several features of the clinical environment, including patient diversity, supervision quality, working conditions, physical facilities, access to equipment, opportunities for active participation, and overall learning experiences. However, existing clinical learning environment instruments are generally developed for specific disciplines and may not fully reflect the needs of students from different health sciences programs.

The study will include fourth-year undergraduate students from health sciences programs who have previously participated in clinical practice or internship training. Students who have not completed clinical placements or who provide incomplete questionnaires will be excluded. Participants will be recruited from Hacettepe University Faculty of Physical Therapy and Rehabilitation and Lokman Hekim University Faculty of Health Sciences using convenience sampling.

The proposed scale is expected to include approximately 31 items covering patient characteristics, supervisor characteristics, working conditions, physical environment and infrastructure, and learning experience. Participants will also provide limited demographic information, including age, sex, department, and clinical placement participation status. Completing the questionnaire is expected to take approximately 10 minutes.

The scale development process will include content validity, construct validity, and reliability analyses. Content validity will be assessed through expert review involving academics from relevant health sciences disciplines. Exploratory and confirmatory factor analyses will be conducted to evaluate the factor structure of the scale. Internal consistency will be assessed using Cronbach's alpha coefficients and corrected item-total correlations.

Participation will be voluntary and anonymous. No intervention, biological sample collection, image recording, or audio recording will be performed. The findings may contribute to the evaluation and improvement of clinical education environments, support student-centered quality assurance processes, and provide a standardized tool for use in health sciences education and accreditation activities.

研究の種類

観察的

入学 (推定)

310

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

サンプリング方法

非確率サンプル

調査対象母集団

The study population will consist of fourth-year undergraduate students enrolled in health sciences programs at Hacettepe University Faculty of Physical Therapy and Rehabilitation and Lokman Hekim University Faculty of Health Sciences. Eligible students will be those who have previously completed or are currently participating in clinical practice, internship, or clinical placement training.

Students from Physiotherapy and Rehabilitation, Nutrition and Dietetics, Speech and Language Therapy, Midwifery, Occupational Therapy, Nursing, and Audiology programs may be included. Participants will be recruited using convenience sampling through relevant academic staff, clinical education settings, and student representatives.

A minimum sample of 310 students is planned, based on the anticipated 31-item scale and the recommendation to recruit at least 10 participants per item for scale development studies. Participation will be voluntary, and all data will be collected anonymously through sel

説明

Inclusion Criteria:

  • Fourth-year undergraduate student enrolled in a health sciences program.
  • Previous or current experience of clinical practice, internship, or clinical placement.
  • Able to read and understand Turkish.
  • Provides voluntary informed consent to participate.

Exclusion Criteria:

  • No previous or current clinical practice, internship, or clinical placement experience.
  • Incomplete questionnaire responses.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
介入・治療
Health Sciences Students with Clinical Placement Experience
Fourth-year undergraduate students enrolled in health sciences programs who have previously completed or are currently completing clinical practice, internship, or clinical placement training. Participants will complete an anonymous questionnaire evaluating their clinical education environment.
Participants completed assessment forms. No intervention was administered.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Exploratory Factor Analysis Factor Loadings
時間枠:Baseline (Day 1)
The factor structure of the newly developed scale will be evaluated using exploratory factor analysis. Factor loadings of the scale items will be examined to determine the contribution of each item to the underlying factor structure. Higher factor loadings indicate stronger association between the item and the relevant factor.
Baseline (Day 1)
Explained Variance in Exploratory Factor Analysis
時間枠:Baseline day 1
The total variance explained by the factor structure identified through exploratory factor analysis will be calculated. A higher percentage of explained variance indicates that the factor structure accounts for a greater proportion of the variability in scale responses.
Baseline day 1
Kaiser-Meyer-Olkin Measure of Sampling Adequacy
時間枠:Baseline (day 1)
The adequacy of the data for factor analysis will be assessed using the Kaiser-Meyer-Olkin measure. Higher values indicate greater suitability of the data for factor analysis.
Baseline (day 1)
Bartlett's Test of Sphericity
時間枠:Baseline (day 1)
The suitability of the correlation matrix for factor analysis will be assessed using Bartlett's test of sphericity. A statistically significant result indicates that the correlation matrix is appropriate for factor analysis.
Baseline (day 1)
Confirmatory Factor Analysis Model Fit Indices
時間枠:Baseline (day 1)
Confirmatory factor analysis will be used to evaluate the fit of the proposed factor structure. Model fit will be assessed using standard fit indices, including chi-square/degrees of freedom, CFI, NFI, NNFI, IFI, SRMR, and RMSEA. Better model fit indices indicate greater support for the proposed factor structure.
Baseline (day 1)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月1日

一次修了 (推定)

2026年9月1日

研究の完了 (推定)

2027年1月1日

試験登録日

最初に提出

2026年7月1日

QC基準を満たした最初の提出物

2026年7月10日

最初の投稿 (実際)

2026年7月16日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月16日

QC基準を満たした最後の更新が送信されました

2026年7月10日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2026-XXÖ

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いいえ

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