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The Effect of Guided Imagery on Bonding and Breastfeeding After Cesarean

Breastfeeding Clinical Trial

Official title:
The Effect of Guided Imagery on Bonding and Breastfeeding After Cesarean; A Randomized Controlled Study

Clinical Trial Summary

The aim of this study is to evaluate the effect of guided imagery after cesarean section on mother-infant bonding and breastfeeding. The study will be carried out in two different groups. The practice will start with meeting the women 6-10 hours after cesarean section. After the women are evaluated in terms of eligibility criteria for the research, the women who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups. Intervention Group; The individuals in this group will be provided with guided imagery application. Guided imagery will be applied to the participants in the hospital environment 6-10 hours after the cesarean section. Afterwards, guided imagery application will be requested every day for two weeks. Control Group; The participants in the control group will perform routine care of the clinic.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05344846
Study type Interventional
Source Ankara University
Contact Zeynep Kaya
Phone 05529209750
Email zeynepbozkurt@tarsus.edu.tr
Status Not yet recruiting
Phase N/A
Start date May 2022
Completion date December 2022
View Details
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