Actively Recruiting
Resilience Enhancement Training Program to Confront Nursing Students' Perceived Stress
Led by Ain Shams University · Updated on 2025-11-17
90
Participants Needed
2
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to assess if a resilience enhancement training program can help nursing students manage stress more effectively. The main question it aims to answer is: Does the program improve nursing students' resilience levels? Does the program lower nursing students' perceived stress levels? Researchers will compare students who receive the training during the semester with students who do not receive it until after the study is completed to see if the training has an effect. Participants will: 1. Complete questionnaires on resilience and stress before and after the training. 2. Attend a structured resilience enhancement training program for 10 weeks alongside their usual studies. 3. Be part of either the study group (receiving the training first) or the comparison group (receiving the training after study completion).
CONDITIONS
Official Title
Resilience Enhancement Training Program to Confront Nursing Students' Perceived Stress
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Nursing students enrolled in the Psychiatric and Mental Health Nursing (PMHN) course at the Faculty of Nursing, Ain Shams University during the first semester of the academic year 2025-2026.
- Willing to participate and able to provide informed consent
You will not qualify if you...
- Students who decline participation or withdraw consent at any time.
- Students absent for the majority of the program sessions.
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Faculty of Nursing, Ain Shams University
Cairo, Cairo Governorate, Egypt, 11566
Not Yet Recruiting
2
Faculty of Nursing, Ain Shams University
Cairo, Cairo Governorate, Egypt, 11566
Actively Recruiting
Research Team
F
Fatma M Ibrahim, PhD
CONTACT
A
Amal E Nossier, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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