- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06318468
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
Status
Recruiting
Conditions
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
- Name: Mei Fen Tang, MSN
- Phone Number: 0970746226
- Email: 5053@w.tmu.edu.tw
Study Locations
-
-
-
Taipei, Taiwan, 116
- Recruiting
- Taipei Municipal Wan Fang Hospital-commissioned by Taipei Medical University / Taipei Taiwan
-
Contact:
- MEI-FEN TANG, PhD
- Phone Number: + 886-2-29307930 ext 8606
- Email: 5053@w.tmu.edu.tw
-
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:
- Mei Fen Tang, master
- Phone Number: 0970746226
- Email: 5053@w.tmu.edu.tw
-
-
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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