- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05903846
The Effect of Oketani Massage on Breastfeeding Success and Breast Engorgement in Mothers Delivering by Cesarean Section
The Effect of Oketani Massage on Breastfeeding Success and Breast Engorgement in Mothers Delivering by Cesarean Section: A Randomized Controlled Study
Study Overview
Status
Intervention / Treatment
Detailed Description
The research was carried out in two groups, namely the octopus massage group and the control group.
Oketani Massage Group: According to the Ministry of Health, the follow-up period for mothers after cesarean section in Turkey is 48 hours. After the mothers in the massage group were taken to the service, oketani massage was applied three times a day for an average of 15-20 minutes, starting before breastfeeding. Massage was applied to the Oketani massage group by a midwife working in the clinic. Before the mothers were discharged, the breast engorgement and breastfeeding status of the mothers were evaluated using the breast fullness assessment scale and the LATCH breastfeeding diagnostic scale. Control Group: No intervention was made in the control group and routine follow-up of mothers and babies will be performed after cesarean section. No intervention was made regarding the breastfeeding process of the mothers, other than the breastfeeding counseling given by the breastfeeding consultant according to the hospital protocol. Before the mothers were discharged, the breast engorgement a and breastfeeding status of the mothers were evaluated using the breast fullness assessment scale and the LATCH breastfeeding diagnostic scale.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Ağrı, Turkey (Türkiye)
- Agri Ibrahim Cecen University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion criteria for the study:
- Delivery by cesarean section
- Single and live birth,
- 38-40 Giving birth between weeks
- Not having a mental or physical disability that prevents breastfeeding,
- The baby does not need neonatal intensive care
- The baby does not have a condition that prevents breastfeeding
- Sharing the same room with the baby
- Agreeing to participate in the research
Exclusion criteria from the study:
- Refusal to participate in the study
- Giving birth normally
- Giving birth prematurely
- Having a mental and physical disability that prevents breastfeeding
- Being 18 years of age or younger
- Transferring the baby to the neonatal intensive care unit
- Having a condition that prevents breastfeeding
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Oketani massage group
According to the Ministry of Health, the follow-up period for mothers after cesarean section in Turkey is 48 hours.
After the mothers in the massage group were taken to the service, oketani massage was applied three times a day for an average of 15-20 minutes, starting before breastfeeding.
Massage was applied to the Oketani massage group by a midwife working in the clinic.
Before the mothers were discharged, the breast fullness and breastfeeding status of the mothers were evaluated using the breast engorgement assessment scale and the LATCH breastfeeding diagnostic scale.
|
The part between the breast and the base of the lower pectoral muscle is called the "oketani".
It is a manual massage technique developed to encourage breastfeeding in breastfeeding problems such as insufficient milk production and mastitis.
It is a massage that stimulates the breast, relaxes it and is painless.
|
|
No Intervention: Control group
No intervention was made in the control group and routine follow-up of mothers and babies will be performed after cesarean section.
No intervention was made regarding the breastfeeding process of the mothers, other than the breastfeeding counseling given by the breastfeeding consultant according to the hospital protocol.
Before the mothers were discharged, the breast fullness and breastfeeding status of the mothers were evaluated using the breast fengorgement assessment scale and the LATCH breastfeeding diagnostic scale.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Breast engorgement assessment scale
Time Frame: postpartum 48 hours from birth
|
The scale is scored from 1 to 6. On the scale, "1" is evaluated as no soft change, while "6" is expressed as very hard and very sensitive.
If the score from the scale is higher than 4, it means that there is breast fullness.
|
postpartum 48 hours from birth
|
|
LATCH breastfeeding diagnostic scale
Time Frame: postpartum 48 hours from birth
|
by observing breastfeeding; It is an assessment tool that is quick and easy to apply, created to detect problems that may occur during breastfeeding.
Scoring is done between 0-2 and the maximum score that can be obtained is 10.
In the non-breakpoint measurement tool, a high score indicates successful breastfeeding.
|
postpartum 48 hours from birth
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AgriIbrahimCecenU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Breastfeeding
-
Uludag UniversityCompletedVirtual Reality | Breastfeeding Education | Breastfeeding Duration | Breastfeeding Self-Efficacy | Metaverse | Breastfeeding Motivation | Digital Museum | Breastfeeding Problems AssessmentTurkey (Türkiye)
-
Marmara UniversityNot yet recruitingBreastfeeding | Breastfeeding Support
-
Halic UniversityCompletedBreastfeeding | Breastfeeding, ExclusiveTurkey
-
University of Ontario Institute of TechnologyDurham Region Health DepartmentUnknown
-
University of California, DavisUniversity of California, San Francisco; Public Hospital Roatan, HondurasCompletedBreastfeeding | Breastfeeding, ExclusiveHonduras
-
T.C. ORDU ÜNİVERSİTESİCompletedBreastfeeding Education | Breastfeeding Attitude | Breastfeeding Self-EfficacyTurkey
-
Semmelweis UniversityNot yet recruitingLactation | Breastfeeding | Breastfeeding Mothers | Breastfeeding Education | Lactating Mother
-
Fundacion Profesor Novoa SantosNot yet recruitingGrowth & Development | Breastfeeding, Exclusive | Breastfeeding Rate | Breastfeeding Outcomes | Breastfeeding Duration | Breastfeeding After Discharge From Hospital Following Childbirth, Yes/no | Breastfeeding Attitude | Breastfeeding Support System | Breastfeeding Consultancy Training | Breastfeeding...Spain
-
Celal Bayar UniversityManisa Celal Bayar UniversityCompletedBreastfeeding | Breastfeeding, ExclusiveTurkey
-
Benten Technologies, Inc.National Institute on Minority Health and Health Disparities (NIMHD); George... and other collaboratorsEnrolling by invitationBreastfeeding | Exclusive BreastfeedingUnited States
Clinical Trials on Oketani massage
-
Saglik Bilimleri UniversitesiRecruiting
-
Mansoura UniversityNot yet recruitingBreastfeeding | Breastfeeding Self-Efficacy | Oketani Massage | LatchingEgypt
-
University of TromsoRecruitingChronic Neck PainNorway
-
Chulalongkorn UniversityCompletedIschemic StrokeThailand
-
Mayo ClinicCompletedFatigue | Stress | Anxiety | TensionUnited States
-
TC Erciyes UniversityCompletedAbdominal Pain | Satisfaction, Patient | DistentionTurkey
-
muxing zhuRecruiting
-
EMRE ERKALCompleted
-
Mersin UniversityCompletedHemodialysis PatientsTurkey
-
Universitat Internacional de CatalunyaUnknown