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"EFFECTS OF PEYTON'S MODEL"

"EFFECTS OF PEYTON'S MODEL AND PEER EDUCATİON ON NURSİNG STUDENTS' URİNE SPECİMEN COLLECTİON SKİLLS FROM URİNARY CATHETERS: A THREE-ARM RANDOMİZED CONTROLLED TRİAL"

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07732049
Acronym
MU-NS-PEYTON26
Enrollment
75
Registered
2026-07-28
Start date
2026-09-15
Completion date
2027-02-01
Last updated
2026-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinical Skills Training, Nursing Education

Keywords

Peyton's Four-Step Approach, Nursing Education, Clinical Skills Training, Sterile Urine Specimen Collection, Simulation-Based Education

Brief summary

Detailed Description This randomized controlled trial aims to compare the effectiveness of three educational approaches in improving nursing students' knowledge, clinical skill performance, and self-efficacy regarding sterile urine specimen collection from an indwelling urinary catheter. The study will be conducted during the Spring semester of the 2025-2026 academic year in the Nursing Skills Laboratory at Maltepe University. The study population will consist of first-year nursing students enrolled in the Fundamentals of Nursing course. Students aged 18 years or older who voluntarily agree to participate will be eligible. Students who have previously received training or have experience in collecting sterile urine specimens from an indwelling urinary catheter will be excluded from the study. Phase 1: Selection and Training of Peer Educators Peer educators will be selected from volunteer fourth-year nursing students who have previous mentoring experience with first-year students and a grade point average above 3.0. Before the intervention, peer educators will receive standardized training from the principal investigator using Peyton's Four-Step Teaching Approach. The training will focus on sterile urine specimen collection from an indwelling urinary catheter and will be based on a validated procedural checklist with excellent reliability. During the training, peer educators will complete all four stages of Peyton's model, including demonstration, deconstruction, comprehension, and performance with structured feedback to ensure standardized instruction throughout the study. Phase 2: Theoretical Education, Baseline Assessment, and Randomization All eligible first-year nursing students will receive a four-hour theoretical lecture delivered by the course instructor before practical training. The theoretical content will include urinary system anatomy and physiology, urinary elimination and assessment, urinary catheterization, sterile urine specimen collection from an indwelling urinary catheter, and prevention of catheter-associated urinary tract infections. Following the theoretical session, participants will complete baseline assessments consisting of a Demographic Information Form, a Knowledge Test, and the Student Self-Efficacy Scale. Participants will then be randomly assigned in a 1:1:1 ratio to one of three study groups: Peyton Four-Step Teaching delivered by the course instructor. Peyton Four-Step Teaching delivered by trained peer educators. Traditional demonstration-based instruction delivered by the course instructor (control group). Randomization will be performed by an independent researcher who is not involved in participant recruitment, intervention delivery, or outcome assessment. A computer-generated block randomization sequence (block size = 6) created using Randomizer.org will be used to ensure balanced allocation among groups. Allocation concealment will be maintained using sequentially numbered, opaque, sealed envelopes. The researcher responsible for outcome assessment will remain blinded to group allocation throughout the study. Phase 3: Practical Skills Training Following randomization, students will receive practical training according to their assigned group. The two intervention groups will be taught using Peyton's Four-Step Teaching Approach by either the course instructor or trained peer educators. This approach consists of demonstration, deconstruction with step-by-step explanation, comprehension through learner-guided instruction, and independent performance with structured feedback. The control group will receive conventional demonstration-based instruction in which the instructor demonstrates and explains the procedure before students independently perform the skill. All practical sessions will be conducted individually in the nursing skills laboratory using simulation manikins. Student performance during training will follow the same validated procedural checklist to ensure standardization across groups. Phase 4: Post-Intervention Assessment After completing the practical training, participants will complete the Knowledge Test, Student Self-Efficacy Scale, and a Student Satisfaction Questionnaire developed by the researchers. Clinical skill performance will be evaluated by a blinded assessor using the validated procedural checklist employed throughout the intervention. Statistical analyses will be performed by an independent researcher who is not involved in the intervention or assessment process. This study is designed to determine whether Peyton's Four-Step Teaching Approach, delivered either by faculty members or trained peer educators, provides superior educational outcomes compared with conventional demonstration-based instruction. Participation in the study is entirely voluntary. The assessments are conducted solely for research purposes and will not contribute to students' course grades, academic achievement, or formal performance evaluation.

Interventions

BEHAVIORALPeyton Four-Step Teaching Model

Participants will receive practical training in sterile urine specimen collection from an indwelling urinary catheter using the Peyton Four-Step Teaching Model. The intervention consists of four sequential steps: demonstration, deconstruction, comprehension, and independent performance with structured feedback. Depending on study group allocation, the training will be delivered either by the course instructor or by trained peer educators. All training sessions will be conducted individually in the nursing skills laboratory using simulation manikins and a standardized procedural checklist to ensure consistency of the educational content and skill assessment

BEHAVIORALTraditional Demonstration-Based Teaching

Participants will receive practical training in sterile urine specimen collection from an indwelling urinary catheter using the traditional demonstration-based teaching method. The course instructor will explain and demonstrate the procedure according to the standardized procedural checklist. Following the demonstration, participants will practice the procedure individually under supervision and receive structured feedback. All training sessions will be conducted in the nursing skills laboratory using simulation manikins and the same standardized procedural checklist used in the intervention groups.

Sponsors

Maltepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Outcome assessment and statistical analyses will be performed by researchers who are blinded to group allocation. Participants and instructors will not be blinded due to the nature of the educational intervention.

Intervention model description

Participants will be randomly assigned in a 1:1:1 ratio to three parallel groups using block randomization with allocation concealment. Two intervention groups will receive Peyton Model-based training delivered by either a faculty member or a trained peer educator, while the control group will receive traditional demonstration-based instruction. Outcome assessment will be performed by a blinded assessor.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* First-year undergraduate nursing students enrolled in the Fundamentals of Nursing course- Aged 18 years or older * No previous formal training in sterile urine specimen collection from an indwelling urinary catheter * Able to communicate in Turkish- Willing to participate in the study and provide written informed consent

Exclusion criteria

* Previous clinical experience involving sterile urine specimen collection from an indwelling urinary catheter * Prior participation in similar educational or simulation training related to the study skill- Failure to attend the theoretical or practical training sessions * Withdrawal from the study at any stage- Incomplete study data

Design outcomes

Primary

MeasureTime frameDescription
Skill performance in sterile urine specimen collection from an indwelling urinary catheterImmediately after completion of the training interventionSkill performance will be evaluated using the Urine Specimen Collection from an Indwelling Urinary Catheter Skills Checklist. Higher scores indicate better procedural skill performance.

Secondary

MeasureTime frameDescription
Knowledge level regarding sterile urine specimen collection from an indwelling urinary catheterBefore the intervention and immediately after completion of the training interventionKnowledge level will be assessed using a researcher-developed knowledge test. Higher scores indicate greater knowledge regarding sterile urine specimen collection from an indwelling urinary catheter.
Self-efficacyBefore the intervention and immediately after completion of the training interventionSelf-efficacy will be assessed using the Student Self-Efficacy Scale. Higher scores indicate greater self-efficacy in performing sterile urine specimen collection from an indwelling urinary catheter.
Student satisfaction with the educational interventionImmediately after completion of the training interventionStudent satisfaction with the educational intervention will be assessed using a researcher-developed satisfaction questionnaire. Higher scores indicate greater satisfaction with the educational method received.

Countries

Turkey (Türkiye)

Contacts

CONTACTEbru Çalışkan, PhD
ebrucaliskan@maltepe.edu.tr+90 5052641381
CONTACTTuğba Bozdemir, PhD
tugbabozdemir@maltepe.edu.tr+90 5520978860
PRINCIPAL_INVESTIGATOREbru Çalışkan, pHd

Maltepe University, Faculty of Nursing

STUDY_DIRECTORTuğba Bozdemir, PhD

Maltepe University, Faculty of Nursing

STUDY_DIRECTORAdife Ahsen ÇETİN

Maltepe University, Faculty of Nursing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 8, 2026