Discharge Training Given to Primiparous Mothers Who Had a Cesarean Delivery

NCT06268028 | Completed

• 1 other identifier: BELMA TA
• Study Type: interventional
• Target: 70
• Locations: 1 country
• Sites: 1

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.

Conditions

Training

Keywords

Training of discharge; Caesarean section; Primiparous

Outcome Measures

Primary Outcomes (1)

• A pre-test applied to 70 women who constitute the sample of the research.

  In 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'.

  16 weeks

Secondary Outcomes (1)

• Apost-test applied to 70 women who constitute the sample of the research.

  16 weeks

Study Arms (2)

EXPERIMENT GROUP

EXPERIMENTAL

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.

Behavioral: Training

CONTROL GROUP

NO INTERVENTION

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.

Interventions

Training BEHAVIORAL

Discharge training

EXPERIMENT GROUP

Eligibility Criteria

• Age: 18 Years - 50 Years
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Able to speak and understand Turkish,
• At least primary school graduate,
• years and over,
• Those who gave birth by cesarean section,
• Primiparous mothers will be included in the research.

You may not qualify if:

• 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.

Sponsors & Collaborators

• Aydin Adnan Menderes University: lead

Study Sites (1)

Aydın Maternity and Child Health Hospital

Aydin, 09010, Turkey (Türkiye)

Location

Study Officials

• BELMA TOPTAŞ ACAR, Res.assist

  Res.assist

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Research Assistant Doctor

Study Record Dates

• First Submitted: February 13, 2024
• First Posted: February 20, 2024
• Study Start: January 10, 2024
• Primary Completion: April 30, 2024
• Study Completion: April 30, 2024
• Last Updated: August 6, 2024

Record last verified: 2024-08

Data Sharing

• IPD Sharing: Will share
• Shared Documents: CSR
• Time Frame: January 10-April 30
• Access Criteria: Clinical Study Report (CSR)

Locations

TU (1)