Effect of Video-Assisted Instruction on Central Venous Catheter Skills in Nursing Students

January 29, 2026 updated by: Bahar Ciftci, Ataturk University

The Effect of Video-Assisted Instruction on Central Venous Catheter Application Skills, Anxiety, and Satisfaction in Nursing Students: A Randomised Controlled Trial

This study aimed to evaluate the effect of video-assisted instruction on central venous catheter (CVC) care skills, anxiety levels, and satisfaction among first-year nursing students. Central venous catheter care requires advanced psychomotor skills and is often associated with anxiety during training.

In this randomized controlled trial, nursing students were assigned to either a video-assisted education group or a traditional education group. Both groups received standard theoretical instruction and laboratory demonstrations. In addition, the intervention group had access to short instructional videos demonstrating blood collection, medication administration, and dressing care related to CVCs.

The primary outcome was students' psychomotor skill performance assessed using an objective structured clinical examination (OSCE). Secondary outcomes included students' state anxiety levels and satisfaction with the training method. The findings of this study are expected to contribute to evidence-based strategies for improving psychomotor skill acquisition in nursing education.

Study Overview

Detailed Description

Nursing education aims to equip students with cognitive, affective, and psychomotor competencies necessary for safe and effective clinical practice. Among these competencies, psychomotor skills related to central venous catheter (CVC) care are complex, technically demanding, and frequently associated with increased anxiety among nursing students. Difficulties in skill acquisition may negatively affect students' confidence and clinical performance.

Video-assisted instruction has emerged as an innovative educational method that allows learners to observe clinical procedures repeatedly, supports self-paced learning, and facilitates the transfer of theoretical knowledge into practice. However, evidence regarding the effectiveness of video-assisted instruction on CVC-related skills, anxiety, and satisfaction remains limited.

This study was designed as a randomized controlled trial conducted at the Faculty of Nursing of Atatürk University between May and July 2024. First-year nursing students who met the inclusion criteria were randomly assigned to either an intervention group or a control group. Both groups received standard theoretical education and laboratory-based demonstrations on CVC care as part of the Fundamentals of Nursing course.

In addition to standard education, students in the intervention group were provided with access to short instructional videos demonstrating CVC blood collection, medication administration, and dressing care. These videos were designed to present each procedure step-by-step and were aligned with the skill evaluation criteria used in the study. The control group did not receive video-based instruction during the study period.

The primary outcome of the study was psychomotor skill performance related to CVC care, assessed using an objective structured clinical examination (OSCE) and a validated CVC Care Skill Evaluation Form. Secondary outcomes included students' state anxiety levels measured using the State Anxiety Inventory and satisfaction with the training method assessed using a structured questionnaire.

Data were collected before and after the educational intervention. The study was conducted in accordance with ethical principles, and written informed consent was obtained from all participants. The results of this study are expected to provide evidence on the effectiveness of video-assisted instruction as a supportive educational strategy for improving psychomotor skills in nursing education and informing future curriculum development.

Study Type

Interventional

Enrollment (Actual)

66

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Erzurum
      • Erzurum, Erzurum, Turkey (Türkiye), 25000
        • Ataturk University Faculty of Nursing

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • First-year nursing students enrolled in the Faculty of Nursing
  • Taking the Fundamentals of Nursing course for the first time
  • Willingness to participate and providing written informed consent
  • Attendance on the days when study data were collected

Exclusion Criteria:

  • Students transferred from another program (horizontal or vertical transfer)
  • Graduates of health vocational high schools
  • Students who withdrew during the study period
  • Students absent during data collection or assessment sessions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Video-Assisted Instruction Group
Participants received standard theoretical and laboratory-based instruction plus video-assisted training on central venous catheter blood collection, medication administration, and dressing care.
Video-Assisted Instruction Group
Active Comparator: Traditional Instruction Group
Participants received standard theoretical and laboratory-based instruction without video-assisted training.
Traditional Instruction Group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall CVC Care Skill Performance Score
Time Frame: 1 week after completion of the training

Overall psychomotor performance in central venous catheter (CVC) care assessed using an Objective Structured Clinical Examination (OSCE).

Participants receive a single total score ranging from 0 to 100 points, where higher scores indicate better overall performance.

1 week after completion of the training

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
State Anxiety Score (State Anxiety Inventory)
Time Frame: 1 week after completion of the training (immediately before OSCE assessment)
Total score of the State Anxiety Inventory (range 20-80). Higher scores indicate higher anxiety.
1 week after completion of the training (immediately before OSCE assessment)
Training Method Satisfaction Score
Time Frame: 1 week after completion of the training (immediately before OSCE assessment)
Total score of the Satisfaction with Training Methods Questionnaire (range 16-80). Higher scores indicate greater satisfaction.
1 week after completion of the training (immediately before OSCE assessment)
Blood Collection Skill Score
Time Frame: 1 week after completion of the training (during OSCE assessment)
Blood collection subscale score of the Central Venous Catheter (CVC) Care Skill Evaluation Form (range 0-36). Higher scores indicate better performance. Assessed during OSCE using the CVC Care Skill Evaluation Form.
1 week after completion of the training (during OSCE assessment)
Medication Administration Skill Score
Time Frame: 1 week after completion of the training (during OSCE assessment)
Medication administration subscale score of the CVC Care Skill Evaluation Form (range 0-30). Higher scores indicate better performance. Assessed during OSCE using the CVC Care Skill Evaluation Form.
1 week after completion of the training (during OSCE assessment)
Dressing Care Skill Score
Time Frame: 1 week after completion of the training (during OSCE assessment)
Dressing care subscale score of the CVC Care Skill Evaluation Form (range 0-34). Higher scores indicate better performance. Assessed during OSCE using the CVC Care Skill Evaluation Form.
1 week after completion of the training (during OSCE assessment)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2024

Primary Completion (Actual)

June 1, 2024

Study Completion (Actual)

July 1, 2024

Study Registration Dates

First Submitted

January 23, 2026

First Submitted That Met QC Criteria

January 29, 2026

First Posted (Actual)

February 4, 2026

Study Record Updates

Last Update Posted (Actual)

February 4, 2026

Last Update Submitted That Met QC Criteria

January 29, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • ATAUNI-CVC-VIDEO-RCT-

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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