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Clinical Trials in Turkey / NCT07575451
Starting soon Not applicable

Empowering Families in Pediatric Cardiovascular Surgery: A RAM-Based Approach

NCT07575451 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-15
Last updated
2026-05-12

Condition(s) studied

Congenital Heart DiseasePostoperative CareChild DevelopmentRoy Adaptation Model-based Nursing Empowerment Program

Investigational drug(s) / intervention(s)

RAM-based Nursing Empowerment ProgramRoutine Care and Educational Booklet

RAM-based Nursing Empowerment Program: RAM-based nursing empowerment program for families of children (ages 1-3) after heart surgery. Includes 5 structured sessions focusing on family empowerment, coping mechanisms, and child development.

Routine Care and Educational Booklet: Families in the control group will receive routine care and an educational booklet titled "Family Empowerment Booklet After Cardiac Surgery Based on Roy Adaptation Model". The booklet provides information on care processes and coping strategies.

Study summary

The purpose of this clinical trial is to learn about the effects of a nursing support program designed for families of children aged 1 to 3 years who have undergone heart surgery. This program aims to improve parents' caregiving skills and support the healthy growth of their children.

The primary questions the study aims to answer are:

Does the nursing program positively affect the physical growth of children, such as their height and weight?

Does the program improve children's scores on general development tests (Denver II)?

Do parents' attitudes toward child feeding and their confidence in parenting skills increase?

Researchers will divide participants into two groups:

Experimental Group: Families who participate in the nursing education program and receive an informative booklet.

Control Group: Families who only receive an informative booklet and continue with routine hospital follow-ups.

The researchers will compare these two groups to see if participating in the nursing program leads to better results for the children's development and the families' skills.

Participants will be asked to:

Attend 5 different education and counseling sessions, starting one week before surgery and continuing until the child reaches 1 year of follow-up.

Meet with the researcher at specific intervals (at 1, 2, 3, 6, 9, and 12 months) for one year to monitor the child's development (height, weight, head circumference) and skills.

Complete surveys regarding child feeding attitudes and parenting skills at the 6th and 12th month follow-ups.

Eligibility

Sex
ALL
Min age
1 Year
Max age
3 Years
Healthy volunteers
No
Inclusion Criteria: * Families who agree to participate in the study and sign the informed consent form. * Families of children aged 1-3 years in the preoperative period who are scheduled to undergo cardiac surgery due to congenital heart disease. * Families who do not speak or read Turkish but will undergo cardiac surgery due to congenital heart disease will also be included in the study with the assistance of an interpreter. * Families who are over 18 years of age and have access to a mobile phone or internet at home. Exclusion Criteria: * Exclusion criteria include the presence of additional congenital malformations, dysmorphic syndromes, chromosomal or endocrine disorders, severe infection, hypothyroidism, or any similar conditions that could lead to growth and developmental delay in the child, alongside congenital heart disease

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Adana City Training and Research Hospital Adana Adana
Cukurova University Adana Adana
Cukurova University Adana Adana

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07575451 on ClinicalTrials.gov ↗ ← All trials in Turkey