العودة إلى لوحة التحكم / Back to Dashboard

The relationship between preoperative anxiety levels and postoperative pain intensity in women undergoing elective cesarean section

ETH-20260304-0132 تاريخ التقديم: Mar 04, 2026 / Submitted: Mar 04, 2026
قيمة الرسوم / Payment Amount
21,000.00 SDG
نوع البحث / Research Type
ورقة علمية / Research Paper
فترة الدراسة / Study Period
Mar 09, 2026 - Jun 10, 2026
Approved
السودان - الولاية الشمالية
وزارة الصحة
الادارة العامة للتخطيط والتنمية الصحية
إدارة البحوث
لجنة الموافقة الأخلاقية
طلب الموافقة الأخلاقية - Ethical Approval Request Form
---
Ethical Approval Request Form
General Administration for Planning and Health Development
Research Department
Ethical Approval Committee
---
رقم التسلسل
Serial Number
SER-20260304-0132
رقم الطلب
Request Number
ETH-20260304-0132
تاريخ تقديم الطلب
Date of Submission
2026-03-04

القسم الأول: معلومات الباحث / Principal Investigator Information

1. الاسم الكامل للباحث الرئيسي
Principal Investigator Full Name
Thoraya Salah Murtada Sidahmed
2. الجهة التي ينتمي إليها
Affiliation Type
جامعة / University: Alzaiem Alazhary University - Faculty of Medicine
Alzaiem Alazhary University - Faculty of Medicine
3. الوظيفة / اللقب العلمي
Job Title/Academic Degree
-
4. البريد الإلكتروني
Email Address
thorayagzzar@gmail.com
5. رقم الهاتف
Phone Number
-
المشرف / Supervisor
الاسم الكامل / Full Name
Mustafa Mohammed
البريد الإلكتروني / Email
-
الوظيفة / اللقب العلمي / Job Title
-
رقم الهاتف / Phone
-
القسم / المؤسسة / Department
-

القسم الثاني: تفاصيل الدراسة البحثية / Research Study Details

7. عنوان الدراسة
Study Title
The relationship between preoperative anxiety levels and postoperative pain intensity in women undergoing elective cesarean section
8. نوع البحث (يرجى التحديد)
Type of Research (Please select)
☐دكتوراه / PhD
☐ماجستير / Master's
☐بكالوريوس / Bachelor's
☐دبلوم عالي / Postgraduate Diploma
☐دبلوم وسيط / Intermediate Diploma
☑ورقة علمية / Research Paper
☐تقرير علمي / Scientific Report
☐أبحاث طبية / Medical Research
☐أخرى / Other
9. وصف مختصر للبحث
Brief Description of Research
Objectives Primary Objective: • To determine whether preoperative anxiety predicts postoperative pain intensity in women undergoing elective cesarean section under spinal anesthesia. Secondary Objectives: 1. To assess the prevalence of high, moderate, and low preoperative anxiety among women undergoing elective CS. 2. To evaluate the association between preoperative anxiety and postoperative analgesic consumption (diclofenac, ibuprofen, paracetamol). 3. To explore the influence of obstetric factors, including previous CS, on postoperative pain levels. 4. To provide evidence for implementing anxiety-reduction interventions to improve postoperative outcomes. Methods Study Design and Setting This study will be conducted in the Northern state Sudan. The study will assess the association between preoperative anxiety and postoperative pain in women undergoing elective cesarean section under spinal anesthesia. Participants A total of 370 women scheduled for elective CS . Inclusion Criteria: • Age ≥18 years and able to give informed consent • Undergoing elective CS under spinal anesthesia • No prior psychiatric or neurological disorders Exclusion Criteria: • Patients receiving general anesthesia • Incomplete data or medical records Data Collection Data will be obtained using a structured data collection sheet including: 1. Sociodemographic characteristics: age, place of residence 2. Obstetric history: parity, history of previous CS 3. Preoperative anxiety assessment: VAS-A (0–10 scale, 0 = no anxiety, 10 = worst anxiety) 4. Postoperative pain assessment: NRS-P (0–10) at 2, 4, 6, and 12 hours post-surgery 5. Postoperative analgesic use: diclofenac, ibuprofen, and paracetamol extracted from medical records Statistical Analysis • Analysis will be conducted using Jamovi software version 2.6.26.

القسم الثالث: الجوانب الأخلاقية / Ethical Considerations

10. طريقة الحصول على الموافقة من المشاركين
Method of Obtaining Consent from Participants
☑مكتوبة / Written
☐شفهية / Verbal
☐غير مطبقة / Not Applicable
☐ضمنية / Implied
☐إعفاء / Waiver
يرجى إرفاق نموذج الموافقة / Please attach consent form
11. آلية الحفاظ على سرية المعلومات
Confidentiality Measures
All participants will receive clear information about the study, including its purpose, procedures, potential risks and benefits, and their right to withdraw at any time without affecting care. Consent will be obtained verbally or in writing, depending on literacy levels.
12. مدى المخاطر على المشاركين
Risk Level to Participants
☐لا توجد / None
☑طفيفة / Minor
☐متوسطة / Moderate
☐عالية / High
يرجى توضيح أي مخاطر محتملة وخطة التعامل معها / Please describe any potential risks and mitigation:
-
13. الفوائد المحتملة للمشاركين أو المجتمع
Potential Benefits to Participants or Society
• Early identification of women with high preoperative anxiety, allowing targeted interventions (e.g., counseling, relaxation techniques) to reduce anxiety before surgery. • Improved postoperative pain management through better understanding of how preoperative anxiety influences analgesic requirements. • Enhanced maternal comfort, faster recovery, and potentially shorter hospital stays by optimizing pain control and psychological support.
14. هل تشمل الدراسة فئات ضعيفة؟
Does the study involve vulnerable groups?
☐الأطفال / Children
☑النساء الحوامل / Pregnant Women
☐اللاجئون/النازحون / Refugees/Displaced
☐ذوو الإعاقة / People with Disabilities
☐أخرى / Other:

القسم الرابع: قائمة المرفقات المطلوبة / Required Attachments

نسخة من المقترح البحثي الكامل
Full Research Proposal
أدوات جمع البيانات
Data Collection Tools
خطاب تسهيل من الجامعة
University Facilitation Letter

القسم الخامس: الإقرار والتوقيع / Acknowledgment and Signature

أُقر أنا الموقع أدناه بأن جميع المعلومات الواردة في هذه الاستمارة صحيحة وكاملة، وأتعهد بعدم البدء في أي جزء من الدراسة قبل الحصول على الموافقة الأخلاقية الرسمية، والالتزام بجميع الإرشادات والمعايير الأخلاقية المعتمدة من قبل لجنة الموافقة الأخلاقية.
I, the undersigned, acknowledge that all information provided in this form is accurate and complete, and I agree not to begin any part of the study before receiving official ethical approval, and to comply with all ethical guidelines and standards approved by the Ethical Approval Committee.
اسم الباحث الرئيسي / Principal Investigator Name
Thoraya Salah Murtada Sidahmed
التوقيع / Signature
_______________________
التاريخ / Date
2026-03-04

معلومات الباحث / Researcher Information

T

Thoraya Salah Murtada Sidahmed

thorayagzzar@gmail.com

جامعة: Alzaiem Alazhary University الكلية: Faculty of Medicine

Dongola Specialized Hospital

اسم المؤسسة التي سيتم فيها عمل البحث / Name of the institution where the research will be conducted

معلومات الدراسة / Study Information

ورقة علمية / Research Paper

messages.degree_research_paper - messages.degree_research_paper

21,000.00 SDG

Objectives Primary Objective: • To determine whether preoperative anxiety predicts postoperative pain intensity in women undergoing elective cesarean section under spinal anesthesia. Secondary Objectives: 1. To assess the prevalence of high, moderate, and low preoperative anxiety among women undergoing elective CS. 2. To evaluate the association between preoperative anxiety and postoperative analgesic consumption (diclofenac, ibuprofen, paracetamol). 3. To explore the influence of obstetric factors, including previous CS, on postoperative pain levels. 4. To provide evidence for implementing anxiety-reduction interventions to improve postoperative outcomes. Methods Study Design and Setting This study will be conducted in the Northern state Sudan. The study will assess the association between preoperative anxiety and postoperative pain in women undergoing elective cesarean section under spinal anesthesia. Participants A total of 370 women scheduled for elective CS . Inclusion Criteria: • Age ≥18 years and able to give informed consent • Undergoing elective CS under spinal anesthesia • No prior psychiatric or neurological disorders Exclusion Criteria: • Patients receiving general anesthesia • Incomplete data or medical records Data Collection Data will be obtained using a structured data collection sheet including: 1. Sociodemographic characteristics: age, place of residence 2. Obstetric history: parity, history of previous CS 3. Preoperative anxiety assessment: VAS-A (0–10 scale, 0 = no anxiety, 10 = worst anxiety) 4. Postoperative pain assessment: NRS-P (0–10) at 2, 4, 6, and 12 hours post-surgery 5. Postoperative analgesic use: diclofenac, ibuprofen, and paracetamol extracted from medical records Statistical Analysis • Analysis will be conducted using Jamovi software version 2.6.26.

Mar 09, 2026 - Jun 10, 2026

Mar 11, 2026 - Mar 31, 2026

الاعتبارات الأخلاقية / Ethical Considerations

Written

مخاطر منخفضة - Low Risk

All participants will receive clear information about the study, including its purpose, procedures, potential risks and benefits, and their right to withdraw at any time without affecting care. Consent will be obtained verbally or in writing, depending on literacy levels.

• Early identification of women with high preoperative anxiety, allowing targeted interventions (e.g., counseling, relaxation techniques) to reduce anxiety before surgery. • Improved postoperative pain management through better understanding of how preoperative anxiety influences analgesic requirements. • Enhanced maternal comfort, faster recovery, and potentially shorter hospital stays by optimizing pain control and psychological support.

Pregnant women