Discharge Training Given to Primiparous Mothers Who Had a Cesarean Delivery

Education Clinical Trial

Official title:

The Effect on the Level of Readiness for Discharge of Discharge Education Given to Primiparous Mothers Having a Cesarean Delivery : A Randomized Controlled Study

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT06268028
• Other study ID #: BELMA TA
• Status: Enrolling by invitation
• Phase: N/A
• Start date: January 10, 2024
• Est. completion date: November 10, 2024

Study information

• Verified date: February 2024
• Source: Aydin Adnan Menderes University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aimed to determine the effect of discharge training given to primiparous mothers who gave birth by cesarean section on the level of readiness for discharge.

The research is a pre-test-post-test, randomized controlled experimental study.

Description:

The research is a pre-test-post-test, randomized controlled experimental study. To prevent selection bias, participants were included in the training and control groups by applying the randomization method. The sample consisted of a total of 70 women (experimental group: 35 women and control group: 35 women). The study was carried out with women who lying to Obstetrics Clinic of Aydın Gynecology and Children's Diseases Hospital and met the study criteria.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 70
• Est. completion date: November 10, 2024
• Est. primary completion date: June 10, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Able to speak and understand Turkish,

• At least primary school graduate,

• 18 years and over,

• Those who gave birth by cesarean section,

• Primiparous mothers will be included in the research.

Exclusion Criteria:

• Those who have a physical disability (vision, hearing, etc.) that prevents them from taking care of themselves,

• In a risky postpartum period,

• Having a history of chronic disease,

• Those who were hospitalized during pregnancy,

• Those who do not have their baby with them after birth,

• Foreign nationals,

• Mothers with psychiatric diagnoses will not be included in the study.

Related Conditions & MeSH terms

• Education

Intervention

Behavioral:
• Training
Discharge training

Locations

Country	Name	City	State
Turkey	Aydin Maternity and Child Health Hospital	Aydin

Sponsors (1)

Lead Sponsor	Collaborator
Aydin Adnan Menderes University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	A pre-test will be applied to 70 women who constitute the sample of the research.	In the pre-test; The individual introduction form and scale will be used, and the same scale will be used for the post-test. Individual Introduction Form: Sociodemographic (Age, educational status, health insurance, etc.) and obstetric characteristics (number of pregnancies, number of miscarriages/abortions etc). (15 questions) (HTHÖ-YDAF): Scale that evaluates readiness for hospital discharge according to the mother's perception; It consists of four subscales and a total of 23 items. The lowest score that can be obtained from the scale is '0' and the highest score is '220'.	up to 5 months
Secondary	Apost-test will be applied to 70 women who constitute the sample of the research.	When the mothers in the training group feel good and ready; Discharge training will be given using the discharge training brochure prepared by the researchers by reviewing the literature. Discharge training will be given one-on-one in the mother's own room, lasting approximately 30-45 minutes. Lectures and question-answer methods will be used as training techniques. If you have any questions after the training, they will be answered. Close to postpartum discharge, mothers in both groups will be asked to fill out the "HTHÖ-YDAF" (post-test) themselves again.	up to 5 months