Breastfeeding Clinical Trial
Official title:
The Effect of Motivational Interviewing-Based Breastfeeding Education on Breastfeeding Motivation, Breastfeeding Success, and Breastfeeding Self-Efficacy Perceptions After Cesarean Section
Verified date | January 2024 |
Source | Selcuk University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The general purpose of this project is; to evaluate effect of motivational interviewing-based breastfeeding education on breastfeeding motivation, breastfeeding success and breastfeeding self-efficacy perception of primiparous mothers after cesarean section. The sub-aims of the study were to evaluate the effect of motivational interviewing-based breastfeeding education on breastfeeding outcomes of primiparous mothers who gave birth by cesarean section. The study will be conducted between September 2022- March 2023 at Konya a private hospital.
Status | Completed |
Enrollment | 76 |
Est. completion date | October 10, 2023 |
Est. primary completion date | March 30, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Volunteer to participate in the study, - Cesarean delivery, - Does not have a condition that prevents breastfeeding, - Married - Primiparous, - Not receiving general anesthesia, - At least primary school graduate, - 18 years and above, - Do not have any chronic disease, - The birth weight of the baby is 2500 g and above, - Your baby's APGAR score is 7 and above in the 5th minute, - Mothers whose babies do not have congenital and/or metabolic diseases will be included in the study. Exclusion Criteria: - Having multiple pregnancy and giving birth, - Foreign nationals and do not speak Turkish, - Having a history of preeclampsia, eclampsia and gestational diabetes, - Mothers who develop complications during cesarean section and whose transfer to the service exceeds 1 hour (because breastfeeding will be delayed for the first hour), - COVID-19 positive in the 1st hour after birth and having a condition that prevents breastfeeding, - Those with a history of diagnosed mental or psychiatric illness will not be included in the study. |
Country | Name | City | State |
---|---|---|---|
Turkey | Medicana Konya Hospital | Konya |
Lead Sponsor | Collaborator |
---|---|
Selcuk University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | LATCH Breastfeeding Assessment Tool | The scale consists of five evaluation criteria and each item is evaluated between 0-2 points. The score that can be obtained from the measurement tool can vary between 0-10. | Change from LATCH Breastfeeding Assessment Tool at 3 months | |
Primary | Breastfeeding Self-Efficacy Short Form Scale | The scale consists of 33 items. It is scored between 1-5 and the lowest 14 and the highest 70 points can be obtained | Change from Breastfeeding Self-Efficacy Short Form Scale at 3 months | |
Primary | The Primipara Breastfeeding Motivation Scale | The Primipara Breastfeeding Motivation Scale: The scale consists of 29 items and is scored between 1-7. It has a total of four sub-dimensions. Evaluation is made by summing the scores obtained in each subgroup in the scale. | Change from The Primipara Breastfeeding Motivation Scale at 3 months | |
Primary | Confidence- sufficiency and importance a scale | It is a grading scale prepared in the form of a visual analog scale. The score that can be obtained from the scale varies in the range of 0-10 points. | Change from Confidence- sufficiency and importance a scale at 3 months | |
Secondary | Rate of feeding the baby with only breast milk | 1st hour after cesarean section, 5-7th days postpartum, postpartum 6th week, and postpartum 3rd month | 3 months | |
Secondary | Total breastfeeding time | 1st hour after cesarean section, 5-7th days postpartum, postpartum 6th week, and postpartum 3rd month | 3 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00579605 -
Motivational Interviewing to Promote Sustained Breastfeeding
|
N/A | |
Completed |
NCT05655364 -
Development of a Breastfeeding Supportive Mobile Application
|
N/A | |
Completed |
NCT03853850 -
Using Mobile Phone Text Messaging System to Improve Exclusive Breastfeeding Rate in a Resource-poor Caribbean Island
|
N/A | |
Completed |
NCT03957941 -
FamilyLink and Breastfeeding
|
N/A | |
Withdrawn |
NCT03709004 -
Pacifiers and Breastfeeding Among Mothers at Risk for Postpartum Depression
|
N/A | |
Completed |
NCT02958475 -
Mother's Milk Messaging: Evaluation of a Bilingual Application (APP) to Support Initiation and Exclusive Breastfeeding in New Mothers
|
N/A | |
Active, not recruiting |
NCT05503069 -
Community Interventions to Improve Breastfeeding
|
N/A | |
Not yet recruiting |
NCT02233439 -
Double-blind, Placebocontrolled A Randomized Trial on the Efficacy of Herbal Galactogogues
|
N/A | |
Completed |
NCT01893736 -
Professional Breastfeeding Support Intervention
|
N/A | |
Completed |
NCT02738957 -
Effect of Prenatal Counseling on Breastfeeding Rates in Twins
|
N/A | |
Completed |
NCT00527956 -
Facilitation and Barriers to Breastfeeding in the NICU
|
N/A | |
Completed |
NCT03655314 -
Using the Electronic Health Record to Guide Management of Newborn Weight Loss
|
N/A | |
Completed |
NCT05106634 -
Evaluation of Breastfeeding Success and Self-Efficacy in Mothers Giving Birth Via Vaginal Delivery or Cesarean Section
|
||
Completed |
NCT05992753 -
Mothers' Breast Milk Expression Experiences, Infant Feeding Attitudes and Perceived Social Support Levels
|
||
Recruiting |
NCT05250219 -
Microchimeric Cell Tranfer From Mother to Child - Pilo Study
|
||
Recruiting |
NCT05213975 -
Kinesio Taping Application After Cesarean Section
|
N/A | |
Recruiting |
NCT05371106 -
Mycotoxins in Mothers Milk in Israel
|
||
Completed |
NCT03332108 -
Novel Approach To Improving Lactation Support With Mobile Health Technology
|
N/A | |
Completed |
NCT02901665 -
Impact of Increased Parent Presence in the Neonatal Intensive Care Unit on Parent & Infant Outcomes
|
N/A | |
Completed |
NCT04037085 -
Ketamine to Improve Recovery After Cesarean Delivery - Part 1
|
Phase 2 |