Effect of an Educational Session for Abortive Women on Maternity Nurses' Practices (NCT07260279) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of an Educational Session for Abortive Women on Maternity Nurses' Practices
Egypt60 participantsStarted 2026-02-01
Plain-language summary
The goal of this study is to evaluate the effect of structured educational sessions for abortive women on the practices of maternity nurses.
The study aims to enhance nurses' clinical skills and patient care related to abortion management.
Participants will:
Attend educational sessions designed to improve nursing practices
Participate in activities and discussions led by experienced instructors
Be observed before and after the sessions to assess changes in clinical practices
The study will compare nursing practices before and after the intervention to determine the overall impact of the educational sessions on professional performance and patient care quality.
Who can participate
Age range
20 Years – 60 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Registered maternity nurses working in obstetrics or gynecology departments.
Having at least one year of clinical experience in maternity or reproductive health units.
Willing to participate and provide informed consent.
Able to read and understand the educational materials provided.
Present at the workplace during the study and follow-up periods.
Not previously involved in similar abortion care training programs.
Exclusion Criteria:
Nurses on maternity or annual leave during the study period.
Administrative or non-clinical nursing staff.
Nurses with less than one year of professional experience.
Refusal to participate or withdrawal at any stage of the study.
Attendance of any concurrent external training on abortion or reproductive health during the study.
Incomplete participation in the educational intervention sessions.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Improvement in maternity nurses' practices regarding abortion care
Timeframe: Before and three months after the educational intervention