Discharge Training Given to Primiparous Mothers Who Had a Cesarean Delivery

NCT ID: NCT06268028

Last Updated: 2024-08-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-01-10
• Study Completion Date: 2024-04-30

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.

Conditions

Training

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

EXPERIMENT GROUP

The individual identification form was first filled out using the face-to-face interview technique. An explanation given regarding filling out the scale and they will be asked to fill it out by self-reporting method under observation. When the mothers in the training group feel good and ready; discharge training gave using the discharge training brochure prepared by the researchers by reviewing the literature. We provided discharge training in the mother's own room and in an average of 30-45 minutes with a one-on-one training method. Mothers asked to fill out the "RHD-NMF" themselves again, close to postnatal discharge.

Group Type: EXPERIMENTAL

Training

Intervention Type: BEHAVIORAL

Discharge training

CONTROL GROUP

Starting from the first (smallest number) room in the clinic, the individual identification form was filled out initially by face-to-face interview technique for mothers who meet the appropriate conditions and agree to participate in the study, according to the randomization order. An explanation given regarding filling out the scale and they will be asked to fill it out by self-reporting method under observation. Mothers asked to fill out the "RHD-NMF" themselves again, close to postnatal discharge.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Training

Discharge training

Intervention Type: BEHAVIORAL

Eligibility Criteria

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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Aydin Adnan Menderes University

OTHER

Sponsor Role: lead

Responsible Party

Belma Toptas Acar

Research Assistant Doctor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

BELMA TOPTAŞ ACAR, Res.assist

Role: PRINCIPAL_INVESTIGATOR

Res.assist

Locations

Aydın Maternity and Child Health Hospital

Aydin, , Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

BELMA TA

Identifier Type: -

Identifier Source: org_study_id