Pain Clinical Trial
— RPCPPWPOfficial title:
Effects of Vibration Techniques and Expiratory Flow Acceleration in Premature Pain Parameters With Pneumonia
Verified date | January 2017 |
Source | Amazon University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Objective to evaluate the effects of vibration techniques and acceleration of expiratory flow on pain parameters in preterm infants diagnosed with pneumonia hospitalized in the Intensive Care Unit and Neonatal Intermediate Care Unit. The Method is a descriptive and interventional study, in which 28 PTNB were randomly divided into two groups: Group 1 submitted to the vibration technique and Group 2 - to the acceleration of the expiratory flow, both techniques were applied in an interval of up to ten minutes, for Three consecutive days. The pain indicators were evaluated according to the PIPP scale in three moments. For statistical analysis, the Friedman tests and Variance Analysis were applied, the level of significance adopted was 5%.
Status | Completed |
Enrollment | 28 |
Est. completion date | November 2016 |
Est. primary completion date | July 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A to 28 Days |
Eligibility |
Inclusion Criteria: - Included in this study were RNPT of both genders, of low weight (1500 to 2500g) or normal weight (over 2500g). - With clinical diagnosis of pneumonia. - Who were on spontaneous ventilation (ambient air or with the aid of oxygen therapy). - Agreed to participate in the research, through the signing of the Informed Consent Form for minors. Exclusion Criteria: - Newborns with a gestational age greater than 37 weeks. - With diseases or procedures that cause pain in the newborn such as necrotizing enterocolitis, thoracotraumatis, thoracic or abdominal drainage, and umbilical catheter. - Who were less than 72 hours Life with birth weight less than 1500g (very low weight and extreme low weight). - As well as those who underwent invasive or non-invasive mechanical ventilation. - Sedated. - With vasoactive drugs or medications that interfered in the physiological parameters of pain. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Amazon University | Fundação Santa Casa de Misericórdia do Pará (FSCMPA) |
Als H, Duffy FH, McAnulty GB, Rivkin MJ, Vajapeyam S, Mulkern RV, Warfield SK, Huppi PS, Butler SC, Conneman N, Fischer C, Eichenwald EC. Early experience alters brain function and structure. Pediatrics. 2004 Apr;113(4):846-57. — View Citation
Brandão AM, Domingues AP, Fonseca EM, Miranda TM, Belo A, Moura JP. [Premature labour with or without preterm premature rupture of membranes: maternal, obstetric and neonatal features]. Rev Bras Ginecol Obstet. 2015 Sep;37(9):428-33. doi: 10.1590/SO100-72 — View Citation
Patel RM, Kandefer S, Walsh MC, Bell EF, Carlo WA, Laptook AR, Sánchez PJ, Shankaran S, Van Meurs KP, Ball MB, Hale EC, Newman NS, Das A, Higgins RD, Stoll BJ; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Resear — View Citation
Silva YP, Gomez RS, Máximo TA, Silva AC. [Pain evaluation in neonatology.]. Rev Bras Anestesiol. 2007 Oct;57(5):565-74. Portuguese. — View Citation
Stevens B, Yamada J, Ohlsson A, Haliburton S, Shorkey A. Sucrose for analgesia in newborn infants undergoing painful procedures. Cochrane Database Syst Rev. 2016 Jul 16;7:CD001069. doi: 10.1002/14651858.CD001069.pub5. Review. — View Citation
Walker CL, Rudan I, Liu L, Nair H, Theodoratou E, Bhutta ZA, O'Brien KL, Campbell H, Black RE. Global burden of childhood pneumonia and diarrhoea. Lancet. 2013 Apr 20;381(9875):1405-16. doi: 10.1016/S0140-6736(13)60222-6. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluation of the parameters of the pain profile scale in preterm infants at different times | The pain indicators of the preterm infants (PIPP) of the two groups were evaluated in three moments, before the application of the technique (T1), immediately after the application of the technique (T2) and 15 minutes After its termination (T3), by a researcher previously trained and blind as to the procedure performed | The total collection period was six months, and each procedure was performed on the volunteers for three consecutive days. |
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