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NCT07514195
MOTHER FRİENDLY PRACTİCES AND MATERNAL, FETAL OUTCOMES
trial in Delivery Care in 281 participants. Completed in 30 September 2025.
31 July 2025
Quick facts
| Lead sponsor | Sakarya University |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 281 |
| Start date | 28 February 2025 |
| Primary completion | 31 July 2025 |
| Estimated completion | 30 September 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Conditions studied
- Delivery Care — all drugs for Delivery Care →
- Satisfaction With Care — all drugs for Satisfaction With Care →
Sponsor
Sakarya University
Who can join
Adults 18 to 45, female only, with Delivery Care or Satisfaction With Care. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The "mother-friendly hospital" model aims to enhance care quality by avoiding unnecessary, non-evidence-based interventions and supporting natural physiological processes from early pregnancy to postpartum. This study evaluated the impact of mother-friendly hospital criteria on labor pain, maternal satisfaction, and maternal and fetal outcomes. Mother-friendly hospital practices emphasizing minimal intervention and physiologic support reduce labor pain, improve maternal satisfaction, and enhance neonatal outcomes. Implementing mother-friendly approaches ensures safe, high-quality, mother-centered maternity care. The results of our study showed that mother-friendly approaches increased maternal satisfaction during the childbirth process and reduced pain scores. These results revealed that mother-friendly practices not only improve the childbirth experience of women but also contribute positively to maternal and neonatal health. Therefore, supporting and expanding the integration of mother-friendly approaches into the healthcare system is of great importance for improving the quality of obstetric services.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07514195
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07514195 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sakarya University
- Last refreshed: 13 April 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07514195.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing