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

被引:16
作者
Brigden, Amberly [1 ]
Beasant, Lucy [1 ]
Hollingworth, William [1 ]
Metcalfe, Chris [2 ,3 ]
Gaunt, Daisy [2 ,3 ]
Mills, Nicola [1 ]
Jago, Russell [4 ]
Crawley, Esther [1 ]
机构
[1] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
[2] Univ Bristol, Bristol Randomised Trials Collaborat, Bristol, Avon, England
[3] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
[4] Ctr Exercise Nutr & Hlth Sci, Sch Policy Studies, Bristol, Avon, England
来源
BMJ OPEN | 2016年 / 6卷 / 07期
关键词
CHRONIC-FATIGUE-SYNDROME; COGNITIVE-BEHAVIOR THERAPY; SPECIALIST MEDICAL-CARE; PHYSICAL-ACTIVITY; ADOLESCENTS; ENCEPHALOMYELITIS; EPIDEMIOLOGY; ANXIETY; PILOT; SCALE;
D O I
10.1136/bmjopen-2016-011255
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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).
引用
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页数:8
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