Effect of Information and Relaxation Exercises on Anxiety Before Cesarean Section
Effects of Planned Pre-Cesarean Information and Progressive Relaxation Exercises on Surgical Fear, Anxiety, Postpartum Comfort and Pain Levels of Primigravida Women: A Randomized Controlled Trial
This study is testing if giving information and teaching relaxation exercises can help first-time moms feel less anxious and more comfortable before their planned cesarean sections.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 68 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | Female |
| Sponsor | Nigde Omer Halisdemir University Academic / other |
| Locations | 1 site (Niğde) |
| Trial ID | NCT06708585 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate how providing information and conducting progressive relaxation exercises can impact surgical fear, anxiety, postpartum comfort, and pain levels in women undergoing planned cesarean sections. The research will involve pregnant women aged 18-35 who are first-time mothers and scheduled for spinal anesthesia. Data will be collected using various scales to assess anxiety and comfort before and after the intervention. The study will be conducted at Ömer Halisdemir University Training and Research Hospital after obtaining necessary ethical approvals.
Who should consider this trial
Good fit: Ideal candidates are first-time pregnant women aged 18-35 who are scheduled for a planned cesarean section with spinal anesthesia.
Not a fit: Patients who experience postpartum complications or require general anesthesia will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety and improve comfort levels for women undergoing cesarean sections.
How similar studies have performed: Previous studies have indicated that interventions aimed at reducing anxiety in surgical settings can be effective, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Between the ages of 18-35, * Primigravida, * Applied for planned cesarean section, * Live singleton pregnancy, * Spinal anesthesia planned, Exclusion Criteria: * Women who develop postpartum maternal or neonatal complications * Receiving general anesthesia.
Where this trial is running
Niğde
- Ömer Halisdemir University Training and Research Hospital — Niğde, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: BİRNUR YEŞİLDAĞ, Dr
- Email: nurumbirnur@gmail.com
- Phone: 05336815923
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.