The Effect of Artificial Intelligence Supported and Nurse-Led Online Breastfeeding Counseling
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorKafkas University
About this trial
Breastfeeding is the gold standard in infant nutrition in the first 12 months of life (1). Breastfeeding self-efficacy perception is one of the most important factors affecting mothers\' breastfeeding duration and success in the postpartum period (2,3).Although AI has traditionally been the domain of powerful mainframes and data centers, new approaches have the capacity to put the power of AI directly into the hands of patients (4).Therefore, considering the importance of breastfeeding education and counseling, this study will determine the effect of training and use of a mobile application-supported artificial intelligence tool and nurse-led online breastfeeding counseling on mothers; breastfeeding self-efficacy perception, breastfeeding success, infant feeding attitude and postpartum depression levels. Thus, the effectiveness of the artificial intelligence tool and nurse-led breastfeeding counseling will be compared.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
The pregnant woman is willing to participate in the research,
The pregnant woman must have an informed written voluntary consent form,
The pregnant woman is over 18 years of age,
The pregnant woman speaks and understands Turkish,
Disqualifiers
The pregnant woman has mental retardation that affects her ability to understand and comprehend,
Multiple pregnancy,
The pregnant woman has gestational disorders such as preeclampsia, eclampsia and a history of gestational diabetes,
The pregnant woman has a diagnosed psychiatric disorder,
Trial design
Design model
Sequential
Treatments tested in this trial
1) Artificial intelligence supported working group
Other interventionPregnant women will be a personal information form, breastfeeding diagnosis and evaluation scale, postnatal breastfeeding self-efficacy scale, Lowa infant nutrition attitude scale and Edinburgh postpartum depression scale. Pregnant women in the artificial intelligence-supported study group were aged 32-37. Starting from the first week of pregnancy, a mobile breastfeeding consultancy application supported by IOS and Android will be installed on smart phones. Pregnant women will be expected to use this application actively until birth and submit their questions about breastfeeding to this artificial intelligence-supported mobile application and receive instant answers. After these applications, the breastfeeding diagnosis and evaluation scale, postnatal breastfeeding self-efficacy scale, Lowa baby nutrition attitude scale and Edinburgh postpartum depression scale will be applied again to pregnant women on the first postpartum day, sixth day, third week and third month.
Online breastfeeding counseling group led by a nurse
Other interventionThe forms that will be applied to pregnant women in all three groups at the first meeting will also be applied to this group. 32-37 in the nurse-led online breastfeeding counseling group. Primiparous pregnant women at the gestational age will be offered 1.5 hours of breastfeeding counseling by one of the researchers, between the 32nd and 37th weeks of pregnancy, with the participation of small groups of five pregnant women in each interactive session. Pregnant women in this group will receive only one session of breastfeeding training. These trainings, which will be given by the nurse, will be carried out online via video call via WhatsApp application. After these applications, the breastfeeding diagnosis and evaluation scale, postnatal breastfeeding self-efficacy scale, Lowa baby nutrition attitude scale and Edinburgh postpartum depression scale will be applied again to pregnant women on the first postpartum day, sixth day, third week and third month.
Treatment groups
90 Participants
are divided into 3 treatment groupsGroup A: 1) Artificial intelligence supported working groupExperimental treatment 1 intervention
Group B: 3) Observation groupNo intervention 0 interventions
Group C: 2)Nurse-led online breastfeeding counseling groupExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
mothers' breastfeeding self-efficacy perception
Breastfeeding Self-Efficacy Scale and Latch Breastfeeding Scale and The Iowa Infant Feeding Attitude Scale will be measured.
Time frame
Measurements will be completed by 12 monthsSecondary outcomes
1
mothers' breastfeeding success
Breastfeeding Self-Efficacy Scale and Latch Breastfeeding Scale and The Iowa Infant Feeding Attitude Scale will be measured.
Time frame
Measurements will be completed by 12 monthsOther outcomes
1
mothers' depression level
Edinburgh Postnatal Depression Scale will be masured.
Time frame
Measurements will be completed by 12 monthsLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: