Proposal for Parental Guidance and Early Stimulation in Children With Congenital Heart Disease: Randomized Trial

Instituto de Cardiologia do Rio Grande do Sul

Status: Completed

Conditions: Congenital Heart Disease

Treatments: Other: Early stimulation protocol on neuropsychomotor development of children with congenital heart disease

Study type: Interventional

Funder types: Other

Identifiers

NCT04152330

5553/18

Details and patient eligibility

About

Problem: With the increased survival rate of children with congenital heart disease, other health problems, in addition to the clinic, have emerged, such as the risks of developmental delay to which these children are exposed. There is a need for low-cost intervention studies that seek to minimize these risks.

Objective: To evaluate the effect of an early stimulation program using parents as vectors of intervention, on the neurodevelopment of children with CHD Methodology: Randomized clinical trial, conducted with 44 dyads of parents-babies with CH considered as medium and high risk for developmental delays according to the guidelines of the American Heart Association (2012). The study will consist of two groups G1 (Intervention) and G2 (controls). G1 parents will receive guidance for 6 weeks of stimulation activities and will be instructed to keep an online execution diary, direct with the researcher through videos, and messages via cell phone. G2 parents will receive the standard guidelines currently used in pediatric cardiology clinics. Children from both groups will be assessed at the beginning and end of the 6 weeks by the Bayley Baby and Toddler Development Scales (3rd Edition). A questionnaire on the applicability of the protocol will be administered to the parents of the intervention group Expected results: Better neuropsychomotor performance in children after applying the early stimulation protocol.

Perspectives: Create a body of information that can serve as a basis for the formulation of policies for intervention and surveillance of the development of this population.

Enrollment: 44 patients

Sex: All

Ages: 3 to 9 months old

Volunteers: No Healthy Volunteers

Inclusion criteria

For babies

• Diagnosis of congenital heart disease up to 3 months old.
• Stable clinical condition (with medical clearance to receive the intervention), For parents
• Parents are literate
• Acceptance of the Responsible to participate in the research.
• Have a mobile device capable of sending and receiving messages and videos.

Exclusion criteria

For babies

• Suspected or diagnosed genetic syndrome;
• Musculoskeletal or neurological malformation associated
• inability to establish a primary caregiver as in the case of baby under state supervision.

for parents

• Illiteracy
• Presence of deafness, blindness or physical disability, when another family member cannot be responsible for the application of the protocol.

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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44 participants in 1 patient group

Comparison between intervention and control group

Other group

Description:

The subjects will be randomized to two groups, intervention group (IG) and control group (CG). Each day GI Parents-Baby receives guidance for 6 weeks of stimulation activities and will be instructed to keep an online execution diary, directly with the researcher of videos and messages via cell phone. "Parents" is understood as a generalist nomenclature and will be considered a parent, mother or principal. GC subjects receive standard guidance from the pediatric and pediatric cardiology clinic.

Treatment:

Other: Early stimulation protocol on neuropsychomotor development of children with congenital heart disease