COPE Program , Mental Health, Mother- Infant Interaction, Sense of Competence

Matrouh University

Status: Completed

Conditions: Outcome; Interaction; Competence; Empowerment

Treatments: Behavioral: Creating Opportunities for Parent Empowerment (COPE) Program

Study type: Interventional

Funder types: Other

Identifiers

NCT06502730

AU-20-4-248

Details and patient eligibility

About

The aim of the study is to:

• Evaluate the effect of creating opportunities for parent empowerment program on maternal sense of competence, mental health outcome and mother-infant interaction.

RESEARCH HYPOTHESES

• Mothers of preterm neonates who receive creating opportunities for parent empowerment program exhibit high level of competence than those who don't.
• Mothers of preterm neonates who receive creating opportunities for parent empowerment program exhibit less stress level than those who don't.
• Mothers of preterm neonates who receive creating opportunities for parent empowerment program exhibit high interaction than those who don't.

The mothers of preterm neonates will be assigned into two equal groups as follows:

• Study group (group II) mothers of preterm neonates who will receive COPE program.
• Control group (group I) mothers of preterm neonates who will not receive COPE program.

Full description

• Research Design: A quasi-experimental (pre-posttest) research design will be used.
• Setting: The study will be conducted at the Neonatal Intensive Care Unit at Smouha Specialty Hospital in Alexandria.
• Subjects: A convenience sampling of 60 mothers of preterm infants who admitted to the previously mentioned setting
• During the 1st day of preterm admission to NICU data concerning characteristics of neonates and their mothers' in both groups will be obtained from medical records using tool I.
• The pretest will be conducted to the mothers of neonates on the 1st day of admission in the NICU to assess mothers' sense of competence and perceived stress by interviewing them to collect data using tool II, III and mother infant interaction in both groups by observation using tool IV.
• After completion of the pretest, the mothers in the study group will receive COPE program, then at the 7th day of the study posttest will be done for both group

Enrollment: 60 patients

Sex: All

Ages: 34 to 37 weeks old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• The mother age more than 20 years, educated and has no experience of premature birth
• The mother has no postpartum discomforts (such as, bleeding, depression or pain
• Premature neonates( gestational age 37 weeks)
• Birth weight < 2500 g or > 1500 g (LBW)
• Five-minute Apgar score > 7
• Neonate not with any medically restricted conditions (e.g., intraventricular hemorrhage or intracerebral hemorrhage (grades III and IV).
• Neonate not on ant ventilation assisted devices, such as ventilator or CPAP

Exclusion criteria

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

60 participants in 2 patient groups

Control group

No Intervention group

Description:

Mothers of preterm neonates who will not receive COPE program.

Study group

Experimental group

Description:

Mothers of preterm neonates who will receive COPE program.

Treatment:

Behavioral: Creating Opportunities for Parent Empowerment (COPE) Program