The Effectiveness of Various Teaching Methods to Enhance the Comprehensive Nursing Assessment Skills of New Nurses

September 15, 2024 updated by: Taipei Medical University WanFang Hospital

Exploring the Effectiveness of Utilizing Various Teaching Methods to Enhance the Comprehensive Nursing Assessment Skills of Newly Recruited Nursing Personnel

This study is going to compare different teaching strategies for improving newly recruited nurses' comprehensive nursing assessment skills.

Study Overview

Detailed Description

Comprehensive nursing assessment is imperative for newly recruited nursing personnel to holistically identify patients' issues, thereby ensuring the provision of high-quality care. This study employs a randomized controlled trial design and will be conducted at a medical center in northern Taiwan. Eligibility criteria for participation require individuals to be new nurses entering the hospital for the first time and lacking prior clinical work experience. Those working part-time will be excluded from the study. A projected enrollment of 60-80 participants includes 30-40 nurses in both the intervention and comparison groups. Nurses assigned to the intervention group will receive nursing health assessment instruction and engage in discussions utilizing humanoid diagrams. In contrast, nurses in the comparison group will undergo health assessment instruction and discussions using case studies. Questionnaires were administered at baseline, immediately post-intervention, and five weeks thereafter to assess the effects of the two training programs.

Study Type

Interventional

Enrollment (Estimated)

80

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 Contact

Study Locations

      • Taipei, Taiwan, 116
        • Recruiting
        • Taipei Municipal Wan Fang Hospital-commissioned by Taipei Medical University / Taipei Taiwan
        • Contact:
        • Contact:
          • Yeu-Hui Chuang, PhD
          • Phone Number: + 886-2-27361661 ext 6328
          • Email: yeuhui@tmu.edu.tw
      • Taipei, Taiwan
        • Not yet recruiting
        • Taipei Medical University WanFang Hospital
        • Contact:

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:

  • nurses who enter the hospital for the first time
  • nurses have not yet gained clinical work experience

Exclusion Criteria:

  • nurses who work in part-time

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Humanoid diagrams training program
The experimental group will receive the nursing health assessment teaching for 50 minutes and discussion using humanoid diagrams for 40 minutes to learn comprehensive nursing assessment.
The experimental group will receive the nursing health assessment teaching for 50 minutes and discussion using humanoid diagrams for 40 minutes to learn comprehensive nursing assessment.
Active Comparator: comparison group
The comparison group will receive health assessment teaching for 50 minutes and discussion using case discussion for 40 minutes to learn comprehensive nursing assessment.
The comparison group will receive the nursing health assessment teaching for 50 minutes and discussion using case study for 40 minutes to learn comprehensive nursing assessment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comprehensive health assessment questionnaire
Time Frame: Baseline, before the intervention(T0)
It is a questionnaire that measures nurses' comprehensive health assessment competency.
Baseline, before the intervention(T0)
Comprehensive health assessment questionnaire
Time Frame: Immediately following after the intervention(T1)
It is a questionnaire that measures nurses' comprehensive health assessment competency.
Immediately following after the intervention(T1)
Comprehensive health assessment questionnaire
Time Frame: Five weeks after the intervention(T2)
It is a questionnaire that measures nurses' comprehensive health assessment competency.
Five weeks after the intervention(T2)
Confidence scale (C-scale)
Time Frame: Baseline, before the intervention(T0)
It is a scale designed to measure participants' confidence in performing the comprehensive nursing assessment.
Baseline, before the intervention(T0)
Confidence scale (C-scale)
Time Frame: Immediately following after the intervention(T1)
It is a scale designed to measure participants' confidence in performing the comprehensive nursing assessment.
Immediately following after the intervention(T1)
Confidence scale (C-scale)
Time Frame: Five weeks after the intervention(T2)
It is a scale designed to measure participants' confidence in performing the comprehensive nursing assessment.
Five weeks after the intervention(T2)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Course satisfaction questionnaire
Time Frame: Immediately following after the intervention(T1)
The scale is designed to measure participants' level of satisfaction with the teaching methods.
Immediately following after the intervention(T1)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Mei Fen Tang, MSN, Taipei Medical University WanFang Hospital

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)

September 4, 2024

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

December 31, 2024

Study Registration Dates

First Submitted

March 12, 2024

First Submitted That Met QC Criteria

March 12, 2024

First Posted (Actual)

March 19, 2024

Study Record Updates

Last Update Posted (Actual)

September 19, 2024

Last Update Submitted That Met QC Criteria

September 15, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • N202306106

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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