Skip to content

Effectiveness of using networks on reducing pain and improving sleep in premature

Effectiveness Positioning Hammock on reducing pain and improving the state of sleep and wakefulness in newborn preterm infants: randomized controlled trial - Hammock: Positioning Hammock

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8s8c8c
Enrollment
Unknown
Registered
2017-11-27
Start date
2016-04-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prematurity

Interventions

Experimental group : Newborns preterm positioned in Hammock . Sample size: 25 patients . The intervention will be maintained for a period of 120 minutes a day for five days. Control group: preterm new
Other

Sponsors

Complexo Hospital de Clínicas da Universidade Federal do Paraná
Lead Sponsor
Complexo Hospital de Clínicas da Universidade Federal do Paraná
Collaborator

Eligibility

Age
24 Weeks to 37 Weeks

Inclusion criteria

Inclusion criteria: Newborns with a gestational age between twelve thirty-seven p.m. weeks; use of non- invasive mechanical ventilation; nasal oxygen catheter; without supplemental oxygen; clinically stable; be admitted to neonatal intensive care unit

Exclusion criteria

Exclusion criteria: Newborns with a gestational age of 37 weeks; clinically unstable; need for invasive mechanical ventilation; neurological or cardiac involvement; bad facial birth defects.

Design outcomes

Primary

MeasureTime frame
Verified by positioning Hammock pain reduction and improvement in the state of sleep and wakefulness newborn preterm ; From the pain assessment scales (PIPP), sleep and wakefulness (adapted from Brazelton Scale); With demonstrated results through percentile, mean, standard deviation

Secondary

MeasureTime frame
Verified by positioning Hammock weight gain and improves the physiological variables of the research subjects; From the measurement of daily weight through a balance and control of physiologica;l parameters through a multiparameter monitor; With results shown by percentiles , mean, standard deviation

Countries

Brazil

Contacts

Public Contactcamila ribas

Complexo Hospital de Clínicas da Universidade Federal do Paraná

camilagemin@hotmail.com+55(41)999239566

Outcome results

None listed

Source: REBEC (via WHO ICTRP)