Evaluation of Breastfeeding Success and Self-Efficacy in Mothers Giving Birth Via Vaginal Delivery or Cesarean Section

NCT ID: NCT05106634

Last Updated: 2023-07-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

106 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-09-10

Study Completion Date

2021-10-22

Brief Summary

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This cross-sectional observational study was conducted to compare breastfeeding success and breastfeeding self-efficacy levels of mothers who gave birth via vaginal delivery (spontaneous or via epidural analgesia) or cesarean section (under general or spinal anesthesia).

Detailed Description

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This study was conducted by including women, who gave birth via VD or CS in the gynecology clinics of a training and research hospital and a city hospital and were in the postpartum period (after 24 hours).

It compared the breastfeeding self-efficacy and breastfeeding success of mothers who gave birth via CS (under spinal anesthesia or general anesthesia) with those of mothers who gave birth via vaginal delivery (under epidural analgesia or via spontaneous vaginal delivery).

Conditions

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Breastfeeding

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

1. being aged \>18 years old;
2. being literate;
3. having a baby of weight between 2500-4000 g, with 5th minute APGAR score of ≥7, and without congenital diseases and sucking and swallowing problems;
4. not having a disease that prevents breastfeeding;
5. having a full-term (37-42 weeks) VD or CS,
6. agreeing to participate in the study

Exclusion Criteria

1. a history of psychological or mental health problems
2. any condition in the mother or infant that was a barrier to breastfeeding
3. baby's admission into the neonatal unit
4. baby's separation from the mother for any reason
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Aydin Adnan Menderes University

OTHER

Sponsor Role lead

Responsible Party

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Gonca Buran

RN, PhD, lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Gonca Buran, PhD

Role: PRINCIPAL_INVESTIGATOR

Uludag Üniversity

Locations

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Ul

Bursa, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Alus Tokat M, Sercekus P, Yenal K, Okumus H. Early postpartum breast-feeding outcomes and breast-feeding self-efficacy in Turkish mothers undergoing vaginal birth or cesarean birth with different types of anesthesia. Int J Nurs Knowl. 2015 Apr;26(2):73-9. doi: 10.1111/2047-3095.12037. Epub 2014 Jun 5.

Reference Type BACKGROUND
PMID: 24897921 (View on PubMed)

Maharlouei N MD, Pourhaghighi A Medical student, Raeisi Shahraki H PhD, Zohoori D MD, Lankarani KB MD. Factors Affecting Exclusive Breastfeeding, Using Adaptive LASSO Regression. Int J Community Based Nurs Midwifery. 2018 Jul;6(3):260-271.

Reference Type BACKGROUND
PMID: 30035142 (View on PubMed)

Other Identifiers

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2019-14/18

Identifier Type: -

Identifier Source: org_study_id

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