Try the modernized ClinicalTrials.gov beta website. Learn more about the modernization effort.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

The Management of Perceived Breastmilk Insufficiency

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04729166
Recruitment Status : Completed
First Posted : January 28, 2021
Last Update Posted : January 28, 2021
Sponsor:
Information provided by (Responsible Party):
Zekiye Karaçam, Aydin Adnan Menderes University

Brief Summary:
A randomized control trial was made to determine the effectiveness of structured education and follow-up in the management of perceived milk insufficiency among breastfeeding mothers.

Condition or disease Intervention/treatment Phase
Breast Milk Expression Breast Feeding, Exclusive Behavioral: Structured education and follow-up Not Applicable

Detailed Description:

Mothers 'perception of breastmilk insufficiency are important conditions affecting babies' exclusively breastfeeding in the first six months.

This study was made to determine the effectiveness of structured education and follow-up in the management of perceived breastmilk insufficiency among breastfeeding mothers. It was tested the hypotheses that there are no differences between mothers who have been provided with structured education and follow-up and those who have not received the education in terms of initiating breastfeeding in the first one hour, breastmilk insufficiency perceptions, the rate of exclusive feeding of breast milk to babies 0-2 months old, the baby's amount of milk intake and weight gain.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 70 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Following recruitment, the pregnant women were divided into a study and a control group by randomization (1:1 randomization)
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Effectiveness of Structured Education and Follow-up on Management of Perceived Breastmilk Insufficiency: A Randomized Control Trial
Actual Study Start Date : December 1, 2018
Actual Primary Completion Date : June 1, 2019
Actual Study Completion Date : June 1, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breastfeeding

Arm Intervention/treatment
Experimental: Study group
The study group were provided with education with structured educational material and followed in this study, in addition to the usual care provided by healthcare professionals.
Behavioral: Structured education and follow-up
This structured educational material was developed by the authors on the basis of the literature. Interventions of the study were carried out in the 32nd-42nd week of pregnancy, 3rd-7th day postpartum, and at the 1st month. At first stage, a 15-20-minute education was given to the pregnant women in the study group in the breastfeeding room of the facility, educational booklets were distributed. The main emphasis parts of the education were repeated with a standard summary information form at each follow-up.

No Intervention: Control group
Control group was int the usual care.



Primary Outcome Measures :
  1. The starting breastfeeding in the first hour [ Time Frame: Postpartum 3rd-7th day ]
    assessed using the Breastfeeding Follow-up Form in 3rd-7th day postpartum. Mothers reported whether they started breastfeeding within the first hour after birth.

  2. Bottle-feeding [ Time Frame: Postpartum 3rd-7th day ]
    assessed using the Breastfeeding Follow-up Form in 3rd-7th day postpartum. Mothers reported whether they feed her baby with bottle-feeding.

  3. The baby's amount of milk intake [ Time Frame: Postpartum 3rd-7th day ]
    assessed using The Scoring System for Measuring a Baby's Intake of Breast Milk. This measurement tool was developed to assess the amount of breast milk a baby is fed. The form is made up of 5 sections: the baby's weight, state of satisfaction, frequency and characteristics of urination and defecation and the condition of the mother's breasts. This tool is filled by observation, measurement and interview. The tool rates each status on the basis of 0, 1 or 2, the highest possible total score being 10. A score of 8-10 indicates that the intake of breast milk is good, 0-7 indicates an insufficient intake.

  4. The baby's amount of milk intake [ Time Frame: Postpartum the 1st month ]
    assessed using The Scoring System for Measuring a Baby's Intake of Breast Milk. This measurement tool was developed to assess the amount of breast milk a baby is fed. The form is made up of 5 sections: the baby's weight, state of satisfaction, frequency and characteristics of urination and defecation and the condition of the mother's breasts. This tool is filled by observation, measurement and interview. The tool rates each status on the basis of 0, 1 or 2, the highest possible total score being 10. A score of 8-10 indicates that the intake of breast milk is good, 0-7 indicates an insufficient intake.

  5. The baby's amount of milk intake [ Time Frame: Postpartum 2nd month ]
    assessed using The Scoring System for Measuring a Baby's Intake of Breast Milk. This measurement tool was developed to assess the amount of breast milk a baby is fed. The form is made up of 5 sections: the baby's weight, state of satisfaction, frequency and characteristics of urination and defecation and the condition of the mother's breasts. This tool is filled by observation, measurement and interview. The tool rates each status on the basis of 0, 1 or 2, the highest possible total score being 10. A score of 8-10 indicates that the intake of breast milk is good, 0-7 indicates an insufficient intake.

  6. Exclusively feeding with mother's milk [ Time Frame: Postpartum 3rd-7th day ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they feed her baby with exclusively mother's milk.

  7. Exclusively feeding with mother's milk [ Time Frame: Postpartum the 1st month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they feed her baby with exclusively mother's milk.

  8. Exclusively feeding with mother's milk [ Time Frame: Postpartum 2nd month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they feed her baby with exclusively mother's milk.

  9. Believing breast milk is adequate [ Time Frame: Postpartum 3rd-7th day ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they believed her baby take adequate breast milk.

  10. Believing breast milk is adequate [ Time Frame: Postpartum the 1st month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they believed her baby take adequate breast milk.

  11. Believing breast milk is adequate [ Time Frame: Postpartum 2nd month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they believed her baby take adequate breast milk.


Secondary Outcome Measures :
  1. Baby's height [ Time Frame: Postpartum 3rd-7th day ]
    used to determine the baby's height. Baby's height was measured and recorded by the researcher to The Breastfeeding Follow-up Form as cm.

  2. Baby's height [ Time Frame: Postpartum 1st month ]
    used to determine the baby's height. Baby's height was measured and recorded by the researcher to The Breastfeeding Follow-up Form as cm.

  3. Baby's height [ Time Frame: Postpartum 2nd month ]
    used to determine the baby's height. Baby's height was measured and recorded by the researcher to The Breastfeeding Follow-up Form as cm.

  4. Believing the baby is adequately fed. [ Time Frame: Postpartum 3rd-7th day ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they believed her baby fed adequate.

  5. Believing the baby is adequately fed. [ Time Frame: Postpartum 1st month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they believed her baby fed adequate.

  6. Believing the baby is adequately fed. [ Time Frame: Postpartum 2nd month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they believed her baby fed adequate.

  7. Being satisfied with baby's weight gain. [ Time Frame: Postpartum 3rd-7th day ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they were satisfied from her baby's weight gain.

  8. Being satisfied with baby's weight gain. [ Time Frame: Postpartum 1st month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they were satisfied from her baby's weight gain.

  9. Being satisfied with baby's weight gain. [ Time Frame: Postpartum 2nd month ]
    assessed using the Breastfeeding Follow-up Form. Mothers reported whether they were satisfied from her baby's weight gain.

  10. Baby's weight [ Time Frame: Postpartum 3rd-7th day ]
    used to determine the baby's weight. Baby's weight was measured and recorded by the researcher to The Breastfeeding Follow-up Form as grams.

  11. Baby's weight [ Time Frame: Postpartum 1st month ]
    used to determine the baby's weight. Baby's weight was measured and recorded by the researcher to The Breastfeeding Follow-up Form as grams.

  12. Baby's weight [ Time Frame: Postpartum 2nd month ]
    used to determine the baby's weight. Baby's weight was measured and recorded by the researcher to The Breastfeeding Follow-up Form as grams.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 35 Years   (Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Gender Eligibility Description:   Pregnant women
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Women in their 32nd-42nd week of pregnancy
  • Being literate in Turkish
  • Being at least a primary school graduate

Exclusion Criteria:

  • Having a history of psychological or mental health problems
  • Having any condition in the mother or infant that was a barrier to breastfeeding
  • The baby's admission into the neonatal unit
  • The baby's separation from the mother for any reason

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04729166


Locations
Layout table for location information
Turkey
Aydın Adnan Menderes University, Faculty of Health Sciences, Division of Midwifery
Aydın, Efeler, Turkey, 09100
Sponsors and Collaborators
Aydin Adnan Menderes University
Investigators
Layout table for investigator information
Study Chair: Zekiye Karaçam, Prof. Dr. Adnan Menderes University, Faculty of Health Sciences, Division of Midwifery
Layout table for additonal information
Responsible Party: Zekiye Karaçam, Professor, Aydin Adnan Menderes University
ClinicalTrials.gov Identifier: NCT04729166    
Other Study ID Numbers: Interventional
First Posted: January 28, 2021    Key Record Dates
Last Update Posted: January 28, 2021
Last Verified: January 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: The data sets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Supporting Materials: Clinical Study Report (CSR)
Time Frame: 6 months after publication
Access Criteria: relevance to the topic of the study and approval of all co-authors within 1 month of receiving the request.

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Zekiye Karaçam, Aydin Adnan Menderes University:
breastmilk
breastfeeding
education
follow-up