Electromyographic Activity of Preterm Newborns Submitted to Hammock Positioning

Instituto Materno Infantil Prof. Fernando Figueira

Status: Unknown

Conditions: Infant, Premature, Diseases

Treatments: Other: Hammock positioning

Study type: Interventional

Funder types: Other

Identifiers

NCT02668107

CAAE 43874915.0.0000.5201

Details and patient eligibility

About

To compare and analyze the effects on the electromyographic activity of preterm newborns placed in the hammock position with the activity of newborns not placed in this position.

Full description

Randomized clinical trial, according to CONSORT standards, with newborn preterm gestational age <34 weeks and birth weight <1500 g, admitted to the intensive care unit. Newborns will be randomized. Those selected for the control group (CG) will be placed in the incubator following the service routine. Babies in the intervention group (IG), will be positioned supine in a hammock in the incubator, with the appropriate postural adjustments. The evaluation of muscle activity will be carried out through surface electromyography. Evaluations shall be performed immediately before the intervention; immediately after 24 hours of intervention; and within 24 hours without intervention, in order to compare the values before and after the intervention of the two groups, as well as if the effects of the intervention are maintained after its removal.

Enrollment: 65 patients

Sex: All

Ages: 1 to 20 days old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Preterm Infants with gestational age <34 weeks
• Free from mechanical ventilation in the last 48 hours prior to electromyographic evaluation
• Not in use of supplemental oxygen at the time of assessment

Exclusion criteria

• Apgar score of less than seven in the fifth minute
• Previous history of perintraventricular hemorrhage grade III and / or IV
• Congenital infection
• Congenital heart defects
• Neonatal Obstetric traumas
• Gastroesophageal Reflux Disease
• Genetic syndromes
• Congenital malformations
• Sepsis with meningitis
• Orthopedic and musculoskeletal alterations

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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65 participants in 2 patient groups

Intervention Group (Hammock positioning)

Active Comparator group

Description:

Babies in the intervention group (IG), will be positioned supine in a hammock in the incubator, with the appropriate postural adjustments.

Treatment:

Other: Hammock positioning

Control Group

No Intervention group

Description:

Those selected for the control group (CG) will be placed in the incubator following the service routine.