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Discharge Training Given to Primiparous Mothers Who Had a Cesarean Delivery

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06268028
Enrollment
70
Registered
2024-02-20
Start date
2024-01-10
Completion date
2024-04-30
Last updated
2024-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Training

Keywords

Training of discharge, Caesarean section, Primiparous

Brief 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.

Detailed 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.

Interventions

BEHAVIORALTraining

Discharge training

Sponsors

Aydin Adnan Menderes University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
A pre-test applied to 70 women who constitute the sample of the research.16 weeksIn the pre-test; The individual introduction form and scale used, and the same scale 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) (RHD-NMF): 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'.

Secondary

MeasureTime frameDescription
Apost-test applied to 70 women who constitute the sample of the research.16 weeksWhen the mothers in the training group feel good and ready; discharge training was provided using the discharge training brochure prepared by the researchers by reviewing the literature. Discharge training gave one-on-one in the mother's own room, lasting approximately 30-45 minutes. Lectures and question-answer methods used as training techniques. Close to postpartum discharge, mothers in both groups asked to fill out the RHD-NMF (post-test) themselves again.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026