Back massage for mothers in the early postpartum period
The Effect of Back Massage Applied to Mothers in the Early Postpartum Period on Comfort, Pain, Anxiety, and Physiological Parameters
This study tests if back massage can help new mothers feel more comfortable and less anxious in the first day after giving birth.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 72 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | T.c. Ordu Üni̇versi̇tesi̇ Academic / other |
| Locations | 1 site (Kahramanmaraş) |
| Trial ID | NCT06200649 on ClinicalTrials.gov |
What this trial studies
This study examines the effects of back massage on mothers within the first 24 hours after vaginal delivery, focusing on various physiological parameters such as comfort, pain, anxiety, and vital signs. By systematically applying massage, the study aims to assess its impact on reducing stress hormones and improving overall well-being during the early postpartum period. The research seeks to fill a gap in existing literature by measuring these specific outcomes, potentially leading to enhanced care practices for postpartum women.
Who should consider this trial
Good fit: Ideal candidates are women aged 18 and over who have had a vaginal delivery and are within the first 24 hours postpartum.
Not a fit: Patients who have undergone cesarean sections or have psychiatric diagnoses may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve comfort and reduce anxiety and pain for mothers in the early postpartum period.
How similar studies have performed: While there are studies on massage and its effects on comfort and anxiety, this specific approach in the early postpartum period is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 and over * Vaginal delivery * In the first 24 hours after birth * First born * Having no difficulty in sitting * Written / verbal communication can be established * At least primary school graduate * Not having any problems during mother's pregnancy * Not diagnosed with any psychiatric disease * Wound, infection, mass etc. on the back. non * Vascular and cardio-thoracic diseases, non-skin diseases * Women who agree to participate in the study will be taken into the sample Exclusion Criteria: * Being under 18 years old * Giving birth by cesarean section * Receiving controlled analgesia after normal delivery * Women with a psychiatric diagnosis will not be included in the study
Where this trial is running
Kahramanmaraş
- Kahramanmaraş, Necip Fazıl City Hospital Gynecology and Pediatrics Additional Service Building — Kahramanmaraş, Turkey (Recruiting)
Study contacts
- Principal investigator: Gamze Şahbaz Çadır, PHD STUDENT — T.c. Ordu Üni̇versi̇tesi̇
- Study coordinator: Gamze ŞAHBAZ ÇADIR
- Email: Gamze.sahbaz46@hotmail.com
- Phone: +90 5067494670
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.