Trial · NCT07894419
Enhancing Male Nursing Students' Competence in Maternity Care: A Quasi-Experimental Study in Egypt
NCT07894419, Not applicable, Active not recruiting, Delta University for Science and Technology
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Enhancing Male Nursing Students' Competence in Maternity Care: A Quasi-Experimental Study in Egypt. Trials, record NCT07894419. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07894419
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Enhancing Male Nursing Students' Competence in Maternity Care: A Quasi-Experimental Study in Egypt
- NCT number
- NCT07894419
- Status
- Active not recruiting
- Phases
- Not applicable
- Enrollment
- 150 participants, actual
- Lead sponsor
- Delta University for Science and Technology
- Conditions
- Maternity Nursing, Obstetric Nursing, Clinical Competence, Simulation Training
- Interventions
- Structured Scenario-Based Clinical Teaching in Maternity Care
- First posted
- 2026-10-26
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Objective Structured Clinical Examination (OSCE) Total Score | Baseline (pre-test) and immediately following the educational intervention (post-test) | Evaluates clinical competence and practical performance across 20 structured examination stations covering obstetric and gynecological nursing skills, clinical calculations, partograph interpretation, and maternity-related interventions. Scored as a mean percentage ranging from 0% to 100%, where higher percentages indicate greater clinical competence, procedural accuracy, and practical performance. |
| Secondary | Change in Student Satisfaction and Self-Confidence in Learning Scores | Baseline (pre-test) and immediately following the educational intervention (post-test) | Assessed using the adapted Student Satisfaction and Self-Confidence in Learning Scale (SSSCL) and adapted Simulation Design Scale. Measured on a 5-point Likert scale ranging from 1 (Strongly Disagree) to 5 (Strongly Agree). Higher total scores indicate higher student satisfaction with learning, increased self-confidence in maternity care, and more positive perceptions of simulation design. |
| Secondary | Change in Practical Performance Checklist Scores | Baseline (pre-test) and immediately following the educational intervention (post-test) | Evaluates procedural competency and accuracy across core maternity nursing skills (such as edema assessment, deep tendon reflex assessment, perineal care, episiotomy care, abdominal and vaginal examinations, and partograph assessment) using a structured observational checklist. Scored on a 3-point rating scale (0 = \\text{Not performed}, 1 = \\text{Performed with assistance}, 2 = \\text{Performed correctly}), converted to a total percentage score. Higher scores indicate better procedural competency and independent performance. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07894419
GET https://conductscience.org/api/trials/v1/NCT07894419/registered