ClinicalTrials.gg
RecruitingNCT07588464(ERAS-NS)Updated May 14, 2026

Effect of ERAS Protocol Education on Nursing Students' Knowledge and Attitudes

An interventional study of ERAS Protocol Education in Nursing Education, sponsored by Istanbul Arel University. Recruiting at 1 site in Turkey (Türkiye). Per ClinicalTrials.gov, last updated 2026-05-14.

Sponsored by Istanbul Arel University · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Jun 2026, 4 months ago, but the record still lists the study as recruiting.
  • Started Apr 2026; still recruiting 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Not applicable
Sex
All
01

Study summary

Enhanced Recovery After Surgery (ERAS) is an evidence-based approach increasingly used in surgical care to improve recovery and reduce postoperative complications. Strengthening nursing students' knowledge of ERAS principles and supporting positive attitudes toward evidence-based nursing are considered important for future professional practice.

This quasi-experimental study was designed to evaluate the effect of ERAS protocol education on nursing students' knowledge levels and attitudes toward evidence-based nursing. The study population consists of undergraduate nursing students enrolled at a university. Data are being collected using a demographic questionnaire, an ERAS knowledge assessment tool, and an evidence-based nursing attitude scale before and after the educational intervention. Statistical analyses are planned to evaluate changes in knowledge levels and attitudes following the intervention.

Read the detailed description

The study aims to investigate the effect of ERAS protocol education on nursing students' knowledge levels and attitudes toward evidence-based nursing. A quasi-experimental pre-test/post-test design is being used. Participants include undergraduate nursing students enrolled at Istanbul Arel University. The educational intervention includes theoretical training on ERAS principles and evidence-based nursing practices. Data are collected before the intervention, one week after the intervention, and one month after the intervention using structured assessment tools. Statistical analyses are planned to evaluate changes in knowledge levels and attitudes toward evidence-based nursing following the educational intervention.

02

Conditions studied

  • Nursing Education

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Keywords

  • ERAS
  • Nursing Students
  • Nursing Education
  • Evidence-Based Nursing
  • Attitude
  • Knowledge
03

In context

Behavior

1,573 studies on the registry are indexed under Behavior; 313 are open to participants now.

This study's planned enrollment of 80 is below the median of 120 across 1,197 interventional studies indexed under Behavior.

Browse Behavior studies →

Lead sponsor

Istanbul Arel University is the lead sponsor of 44 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Being a 4th-year nursing student
  • Actively attending clinical internship during the study period
  • Voluntary participation in the study after being informed
  • Willingness to complete pre-test, educational intervention, and follow-up assessments (1 week and 1 month)

Exclusion criteria

Exclusion Criteria:

  • Not being a 4th-year nursing student
  • Inability to attend education or assessment sessions regularly
  • Refusal to participate in the study
  • Withdrawal from the study during the process
  • Incomplete participation in education or measurement sessions
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    ERAS Education Group

    Nursing students will receive structured education on the Enhanced Recovery After Surgery (ERAS) protocol. The intervention will include theoretical training sessions. No clinical intervention will be applied. Participants' knowledge and attitudes will be assessed before and after the intervention.

    Other: ERAS Protocol Education

Interventions

  • OtherERAS Protocol Education

    Structured theoretical education on ERAS principles for nursing students.

06

What researchers measure

Primary outcomes

  1. ERAS Knowledge Score

    Knowledge regarding the Enhanced Recovery After Surgery (ERAS) protocol will be assessed using a 20-item structured questionnaire developed for this study. Total scores will range from 0 to 100, with higher scores indicating greater knowledge of ERAS principles.

    Time frame: Baseline (pre-intervention), 1 week after intervention, 1 month after intervention

Secondary outcomes

  1. Evidence-Based Nursing Attitude Score

    Attitudes toward evidence-based nursing will be assessed using a Likert-type Evidence-Based Nursing Attitude Scale. Participants will rate items on a 5-point Likert scale. Higher total scores will indicate more positive attitudes toward evidence-based nursing practice.

    Time frame: Baseline (pre-intervention), 1 week after intervention, 1 month after intervention

07

Study locations

1 of 1 sites recruiting
  • Istanbul Arel University Cevizlibağ Health Campus
    Istanbul, Zeytınburnu 34010, Turkey (Türkiye)
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — This study does not involve individual patient data. The data consist of nursing students' questionnaire responses collected for educational research purposes; therefore, individual participant data sharing is not applicable.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2026 (actual). Primary completion is estimated for Jun 2026, 2 months after the start.

Of 741 non-industry interventional studies with no phase under Behavior, half reached primary completion within 14 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 32. This study's planned 2 months is below that.

Counting every sponsor, half of 757 studies reached it within 13 months; a quarter within 5 and three quarters within 32.

How these figures are worked out, and which studies are left out of them.

Registered
May 5, 2026
First posted
May 14, 2026
StartActual
Apr 10, 2026
Primary completionEst.
Jun 30, 2026
CompletionEst.
Jun 30, 2026
Last update
May 14, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07588464
Lead sponsor
Istanbul Arel University
Responsible party
Yesim OZTURK (Graduate Nursing Student, Istanbul Arel University) — Principal investigator
First posted
May 14, 2026
Start date
Apr 10, 2026
Primary completion
Jun 30, 2026 (estimated)
Completion
Jun 30, 2026 (estimated)
Last update
May 14, 2026

Study contacts

YESIM OZTURK, Master's
Contact
yesimozturk25@istanbularel.edu.tr
+90 5396910129
BURCU D DEMIR, PhD
Contact
burcudemir@arel.edu.tr
+90 5069541667
BURCU D DEMIR, PhD
study director · Istanbul Arel University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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