A digital health peri-operative cognitive-behavioral intervention to prevent transition from acute to chronic postsurgical pain in adolescents undergoing spinal fusion (SurgeryPalTM): study protocol for a multisite randomized controlled trial

被引:9
|
作者
Rabbitts, Jennifer A. [1 ,2 ]
Zhou, Chuan [3 ,4 ]
de la Vega, Rocio [5 ]
Aalfs, Homer [3 ]
Murray, Caitlin B. [2 ,3 ]
Palermo, Tonya M. [2 ,3 ,4 ]
机构
[1] Seattle Childrens Hosp, Ctr Clin & Translat Res CCTR, 4800 Sand Point Way NE MB-11-500-3, Seattle, WA 98105 USA
[2] Univ Washington, Dept Anesthesiol & Pain Med, 1959 NE Pacific St, Seattle, WA 98195 USA
[3] Seattle Childrens Hosp, Ctr Child Hlth Behav & Dev CHBD, 1920 Terry Ave, Seattle, WA USA
[4] Univ Washington, Dept Pediat, 4800 Sand Point Way NE, Seattle, WA 98105 USA
[5] Univ Malaga, Dept Psychol, Campus Teatinos S-N, Malaga 29071, Spain
基金
美国国家卫生研究院;
关键词
Adolescent scoliosis; Acute pain; Chronic pain; Psychosocial intervention; mHealth; Randomized controlled trial; GENERIC CORE SCALES; QUALITY-OF-LIFE; POSTOPERATIVE PAIN; RISK-FACTORS; PSYCHOSOCIAL PREDICTORS; PEDIATRIC ACUTE; SLEEP PATTERNS; CHILDREN; PREVALENCE; MANAGEMENT;
D O I
10.1186/s13063-021-05421-3
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Spinal fusion surgery is associated with severe acute postsurgical pain and high rates of chronic postsurgical pain in adolescents. Psychological distress, sleep disturbance, and low pain self-efficacy predict higher acute pain and likelihood of developing chronic postsurgical pain. Interventions targeting baseline psychosocial risk factors have potential to interrupt a negative trajectory of continued pain and poor health-related quality of life (HRQL) over time but have not yet been developed and evaluated. This randomized controlled trial will test effectiveness of a digital peri-operative cognitive-behavioral intervention (SurgeryPal(TM)) vs. education-control delivered to adolescents and their parents to improve acute and chronic pain and health outcomes in adolescents undergoing spine surgery. Methods Adolescents 12-18 years of age undergoing spinal fusion for idiopathic conditions, and their parent, will be recruited from pediatric centers across the USA, for a target complete sample of 400 dyads. Adolescents will be randomized into 4 study arms using a factorial design to SurgeryPal(TM) or education control during 2 phases of treatment: (1) pre-operative phase (one-month before surgery) and (2) post-operative phase (1 month after surgery). Acute pain severity and interference (primary acute outcomes) and opioid use will be assessed daily for 14 days following hospital discharge. Chronic pain severity and interference (primary acute outcomes), as well as HRQL, parent and adolescent distress, sleep quality, and opioid use/misuse (secondary outcomes), will be assessed at 3 months and 6 months post-surgery. Discussion Demonstration of effectiveness and understanding optimal timing of perioperative intervention will enable implementation of this scalable psychosocial intervention into perioperative care. Ultimately, the goal is to improve pain outcomes and reduce reliance on opioids in adolescents after spine surgery.
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页数:12
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