L'effet de la présence du père en salle d'opération sur la qualité de récupération de la parturiente
L'effet de la présence du père pendant la césarienne programmée sous rachianesthésie sur la qualité de récupération de la parturiente
The presence of a partner to support the mother during cesarean and vaginal deliveries is a well-established practice in most countries worldwide. It is evident that allowing the partner into the operating room during a cesarean section provides psychosocial benefits for both the mother and the partner. This study aims to investigate the effect of the presence of partner in the operating room on quality of recovery of parturients at the postoperative period.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
This prospective study evaluates the impact of the partner's presence in the operating room during elective cesarean sections on maternal anxiety, postoperative recovery, and surgeon stress levels. Patients are allocated into two groups: Partner Present and Partner Absent. Primary outcome is obstetric quality of recovery scale (ObsQoR 10) at the postoperative first day. Secondary outcomes include maternal pain (assessed via VAS at 6-hour intervals for the first 24 hours) and anxiety levels (STAI-T/S administered to couples preoperatively and STAI-S postoperatively) and ObsQoR-10 that will be evaluated at the postoperative 3rd and 7th days.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
-
Karaman, Turquie (Türkiye), 70200
- Karaman Training and Research Hospital
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Patients scheduled for an elective cesarean section.
- Patients and their partners must be literate in Turkish (able to read and write) to accurately complete the study questionnaires
- Patients and their partners must be willing and able to provide written informed consent
- Healthy pregnant women with no additional chronic or systemic diseases (comorbidities)
- The operating surgeon must have at least 5 years of professional experience and no chronic health conditions.
Exclusion Criteria:
- Patients undergoing emergency cesarean sections.
- Patients with any known chronic or systemic additional diseases
- Surgeons with any known chronic or systemic diseases.
- Individuals unable to read or understand the Turkish questionnaires (implied by the literacy requirement).
- Patients with American Society of Anesthesiologists (ASA) classification of 3 or more
- Patients with history of chronic pain, chronic use of analgesic drugs, or history of opioid or intravenous drug abuse
- Patients who have refused spinal anesthesia, or those in whom it is contraindicated.
- Pregnancy with preeclampsia or eclampsia
- Pregnancy with gestational diabetes mellitus or diabetes mellitus
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Dépistage
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Partenaire présent
|
The patient's partner is admitted to the operating room after sterile preparations are complete. The partner remains with the patient to provide physical and emotional support during the cesarean section operation |
|
Comparateur actif: Partenaire absent
|
The patient undergoes the elective cesarean section according to standard hospital protocols. The partner is not present in the operating room during the surgery. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Obstetric Quality of Recovery-10 (ObsQoR-10) Score
Délai: Post-operative 24th hour,
|
The ObsQoR-10 questionnaire will be used to assess the quality of maternal recovery after the cesarean section. The scale consists of 10 items, where patients rate each item from 0 (never) to 10 (always). Higher scores indicate a better quality of recovery. |
Post-operative 24th hour,
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Surgeon's Physiological Stress Level (Heart Rate)
Délai: Intra-operative (during the entire duration of the cesarean section)
|
The operating surgeon's heart rate variability will be recorded using a rhythm Holter device during the surgery. A heart rate exceeding 100 beats per minute (bpm) will be considered an indicator of increased stress. |
Intra-operative (during the entire duration of the cesarean section)
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Maternal and Partner Anxiety Levels (STAI-T and STAI-S)
Délai: Pre-operative and Post-operative (within the first 6 hours)
|
The State-Trait Anxiety Inventory (STAI) will be used to measure the patient's and partner's anxiety levels. Both the Trait (STAI-T) and State (STAI-S) components will be administered. Scores range from 20 to 80, with higher scores indicating greater anxiety. |
Pre-operative and Post-operative (within the first 6 hours)
|
Collaborateurs et enquêteurs
Parrainer
Publications et liens utiles
Publications générales
- faruk
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- E-11095095-050.04-253322
Informations sur les médicaments et les dispositifs, documents d'étude
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