Interventions with Music in PECTus excavatum treatment (IMPECT trial): a study protocol for a randomised controlled trial investigating the clinical effects of perioperative music interventions

• Published in: BMJ open Vol. 10; no. 7; p. e036380
• Main Authors: Billar, Ryan J, Kühlmann, A Y Rosalie, Schnater, J Marco, Vlot, John, Tomas, Jeremy J P, Zijp, Gerda W, Rad, Mandana, de Beer, Sjoerd A, Stevens, Markus F, Poley, Marten J, van Rosmalen, Joost, Jeekel, Johannes F, Wijnen, Rene M H
• Format: Journal Article
• Language: English
• Published: England BMJ Publishing Group LTD 08-07-2020; BMJ Publishing Group
• Series: Protocol
• Subjects: Adolescent; Adult; Analgesics, Opioid; Anxiety; Child; Epidural; Funnel Chest - surgery; General anesthesia; Hospitals; Humans; Intervention; Morphine; Multicenter Studies as Topic; Music; Music Therapy; Narcotics; Netherlands; Outpatient care facilities; Pain; Pain, Postoperative - prevention & control; Patients; Pediatrics; Perioperative care; Postoperative period; Quality of Life; Randomized Controlled Trials as Topic; Surgery; Teenagers; Netherlands; paediatric thoracic surgery; paediatric anaesthesia; pain management
• ISSN: 2044-6055; 2044-6055
• DOI: 10.1136/bmjopen-2019-036380

IntroductionPectus excavatum repair is associated with substantial postoperative pain, despite the use of epidural analgesia and other analgesic regimens. Perioperative recorded music interventions have been shown to alleviate pain and anxiety in adults, but evidence for children and adolescents is still lacking. This study protocol describes a randomised controlled trial that evaluates the effects of recorded music interventions on postoperative pain relief in children and adolescents after pectus excavatum repair.MethodsA multicentre randomised controlled trial was set up comparing the effects of perioperative recorded music interventions in addition to standard care with those of standard care only in patients undergoing a Nuss procedure for pectus excavatum repair. One hundred and seventy subjects (12–18 years of age) will be included in three centres in the Netherlands. Patient inclusion has started in November 2018, and is ongoing. The primary outcome is self-reported perceived pain measured on the visual analogue scale. Secondary outcomes are anxiety level, analgesics consumption, vital parameters such as heart rate, blood pressure and respiratory rate, length of hospital stay, postoperative complications, quality of life and cost-effectiveness.Ethics and disseminationThis study is being conducted in accordance with the Declaration of Helsinki. The Medical Ethics Review Board of Erasmus University Medical Centre Rotterdam, The Netherlands, has approved this protocol. Results will be disseminated via peer-reviewed scientific journals and conference presentations.Trial registration numberNL6863