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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06070792
Other study ID # NLP, PMRE, AND BREASTFEEDING
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2023
Est. completion date December 31, 2023

Study information

Verified date October 2023
Source University of Gaziantep
Contact AYSEGÜL KILIÇLI
Phone (0414) 317 17 17
Email aysegul_ay_9@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The effect of neuro linguistic program and progressive muscle relaxation exercises on breastfeeding success and breastfeeding self-efficacy after caesarean section.


Description:

In this research, it is aimed to detemine the effect of neuro linguistic program and progressive muscle relaxation exercises on breastfeeding success and breastfeeding self-efficacy after caesarean section. Sample size: - There will be three groups in the study (two experimental groups and one control group). - The sample size of the study is 99 people. The sample size will be divided into three and 33 people will be randomly assigned to each group. - Experiment 1 group: neuro linguistic programme (NLP) group. - Experiment 2 group: progressive muscle relaxation exercises (PMRE) group. - Control group: non-intervention group Data Collection Tools; - Introductory Information Form, - Breastfeeding Self-Efficacy Scale, - Breastfeeding Charting System (LATCH) Application time: - NLP and PMRE interventions will be started at the sixth postoperative hour after caesarean section. - Mothers who give birth by caesarean section are followed up in hospital for 48 hours and mothers are then discharged when their health condition improves. Therefore, data will be collected within 48 hours after caesarean section. - NLP and PMRE groups will be started at the sixth postoperative hour, 3 times in 24 hours on the first day, 3 times in 24 hours on the second day, six times in total. - Only NLP and PMRE will not be applied to the control group. - Care and follow-up will be performed in parallel with the individuals in the experimental group. Measurement time: - Mothers will fill in the Introductory Information Form, Breastfeeding Self-Efficacy Scale, Breastfeeding Diagnosis and Assessment Measurement Tool (LATCH) before the application at the sixth postoperative hour. - Then, in the first 24 hours, the necessary application will be performed once every eight hours according to the groups (for example, NLP application for experiment 1). - At the end of 24th hour, Breastfeeding Self-Efficacy Scale and Breastfeeding Diagnosis and Assessment Measurement Tool (LATCH) will be completed. - Then, in the second 24 hours, the interventions will be repeated once every eight hours. - The total number of application sessions is six. - NLP application will last 20 minutes each session and PMRE application will last 20 minutes each session.


Recruitment information / eligibility

Status Recruiting
Enrollment 99
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 19 Years to 35 Years
Eligibility Inclusion Criteria: - women who gave birth by caesarean section, - primiparous, - who are 19 years of age or older and 35 years of age or younger, - who were born at 37 or more weeks of gestation, - who had a singleton birth, - whose caesarean section operation was performed with spinal anaesthesia, - who do not have chronic diseases and any breast-related health problems . Exclusion Criteria: - mothers who did not meet the inclusion criteria, - who wanted to leave the study voluntarily at any stage after being included in the study, - who developed any health problems in themselves or their infants were excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
NEURO LINGUISTIC PROGRAM
NEURO LINGUISTIC PROGRAM
PROGRESSIVE MUSCLE RELAXATION EXERCISES
PROGRESSIVE MUSCLE RELAXATION EXERCISES

Locations

Country Name City State
Turkey Sanliurfa training and research hospital Sanliurfa Eyalet/Yerleske

Sponsors (1)

Lead Sponsor Collaborator
Aysegul Kilicli

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary BREASTFEEDING SUCCESS Breastfeeding Charting System (LATCH); The measurement tool has no cut-off point, and as the LATCH score increases, it is understood that the process is high. The maximum score that can be obtained is 10. The sum of lower scores indicates that the mother is dependent on help. immediately before the first application
Primary BREASTFEEDING SUCCESS Breastfeeding Charting System (LATCH) immediately after the third application (at the 24th hour after the first application)
Primary BREASTFEEDING SUCCESS Breastfeeding Charting System (LATCH) immediately after the sixth application (at the 48th hour after the first application)
Primary BREASTFEEDING SELF-EFFICACY Breastfeeding Self-Efficacy Scale; A minimum of 14 points and a maximum of 70 points can be obtained from the scale. All are positive elements. The higher the score from the scale, the higher breastfeeding self-efficacy will be achieved. immediately before the first application
Primary BREASTFEEDING SELF-EFFICACY Breastfeeding Self-Efficacy Scale immediately after the third application (at the 24th hour after the first application)
Primary BREASTFEEDING SELF-EFFICACY Breastfeeding Self-Efficacy Scale immediately after the sixth application (at the 48th hour after the first application)
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