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Managed Activity Graded Exercise iN Teenagers and pre-Adolescents (MAGENTA) feasibility randomised controlled trial:study protocol

机译:青少年和未成年人(MAGENTA)的受控活动分级锻炼可行性随机对照试验:研究方案

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摘要

Introduction Paediatric chronic fatigue syndrome or myalgic encephalomyelitis (CFS/ME) is a relatively common and disabling condition, yet there is a limited evidence base for treatment. There is good evidence that graded exercise therapy is moderately effective in adults with CFS/ME, but there is little evidence for the effectiveness, cost-effectiveness, acceptability or best method of delivery for paediatric CFS/ME. This study aims to investigate the acceptability and feasibility of carrying out a multicentre randomised controlled trial investigating the effectiveness of graded exercise therapy compared with activity management for children/teenagers who are mildly or moderately affected with CFS/ME.Methods and analysis 100 paediatric patients (8–17 years) with CFS/ME will be recruited from 3 specialist UK National Health Service (NHS) CFS/ME services (Bath, Cambridge and Newcastle). Patients will be randomised (1:1) to receive either graded exercise therapy or activity management. Feasibility analysis will include the number of young people eligible, approached and consented to the trial; attrition rate and treatment adherence; questionnaire and accelerometer completion rates. Integrated qualitative methods will ascertain perceptions of feasibility and acceptability of recruitment, randomisation and the interventions. All adverse events will be monitored to assess the safety of the trial.Ethics and dissemination The trial has received ethical approval from the National Research Ethics Service (South West—Frenchay 15/SW/0124).Trial registration number ISRCTN23962803; Pre-results.
机译:引言小儿慢性疲劳综合症或肌性脑脊髓炎(CFS / ME)是一种相对普遍且致残的疾病,但治疗的证据基础有限。有充分的证据表明,分级运动疗法对CFS / ME的成年人有效,但很少有证据证明小儿CFS / ME的有效性,成本效益,可接受性或最佳分娩方法。这项研究旨在探讨进行多中心随机对照试验的可行性和可行性,该试验研究分级运动疗法与轻度或中度CFS / ME影响儿童/青少年的活动管理相比的有效性。方法和分析100名儿科患者(将从3名英国国家卫生局(NHS)的CFS / ME专业服务机构(浴,剑桥和纽卡斯尔)招募具有CFS / ME服务的8-17年。患者将被随机(1:1)接受分级运动疗法或活动管理。可行性分析将包括有资格,接近并同意参加试验的年轻人数量;损耗率和治疗依从性;问卷和加速度计完成率。综合定性方法将确定招募,随机化和干预的可行性和可接受性的看法。将监测所有不良事件,以评估试验的安全性。伦理与传播该试验已获得美国国家研究伦理服务(西南地区,Frenchay 15 / SW / 0124)的伦理批准。试验注册号ISRCTN23962803;结果。

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