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. 2017 Jan 13;7(1):e012633. doi: 10.1136/bmjopen-2016-012633

Table 1.

Table of included studies

Participant characteristics
Study Country Setting CFS/ME diagnostic criteria Number of participants Age range (years) Males/females Illness duration Aim Data collection Data analysis
Jelbert et al47 UK Outpatient clinic None specified.
Clinical diagnosis of CFS/ME
5 13–18 1:4 1.5–2 years Recovered adolescent experiences of CFS/ME Semistructured interviews Interpretative phenomenological analysis
Fisher and Crawley48 UK Outpatient clinic None specified.
Clinical diagnosis of CFS/ME. Above the 90th percentile cut-off on SCAS Scale
11 12–18 2:9 NS Anxious young people's experiences of CFS/ME Interviews Interpretative phenomenological analysis
Hareide et al54 Norway Hospital Modified version of the CDC criteria—3 rather than 6 months duration of fatigue 9 12–17 NS 2.5 years Illness beliefs and coping strategies among adolescents with CFS/ME Semistructured interviews Thematic analysis
Winger et al51 Norway Hospital and primary care 3 months of unexplained fatigue (RCPCH and NICE) 17 12–18 5:12 NS Experience of being an adolescent with CFS/ME In-depth interviews Phenomenological hermeneutical design
Beasant et al55 UK Specialist CFS/ME service NICE 2007. Mild to moderately affected 12 12–18 3:9 9–18 months Experiences of adolescents and families accessing a specialist service In-depth interviews Thematic analysis
Crix et al46 UK Hospital None specified.
Clinical diagnosis of CFS/ME
1 16 0:1 1–2 years How members of one family define and understand a contested diagnosis through talk Family interview Discourse analysis
Ashby et al49 UK CAMHS None specified.
Clinical diagnosis of CFS/ME
10 8–16 3:7 3 months–2 years Service users’ perceptions of the treatment they received Semistructured interviews None specified
Patel52 UK Specialist CFS/ME service NICE 2007, mild to moderately affected (not housebound) 7 8–16 5:2 NS Illness domains that are important to young people with CFS/ME and their parents Semistructured interviews
Focus group with three mothers
Thematic analysis
Williams-Wilson53 UK Specialist CFS/ME service Clinical diagnosis of CFS/ME 8 11–18 2:6 NS Personal experiences of young people with CFS/ME Open-ended interviews Thematic analysis
Lombard50 South Africa Through medical doctors CDC 2 17 2:0 NS Description of living with CFS/ME to create guidelines Interviews, document analysis and observation Phenomenology

CAMHS, child and adolescent mental health service; CFS/ME, chronic fatigue syndrome/myalgic encephalomyelitis; NS, not stated; RCPCH, Royal College of Paediatrics & Child Health; SCAS, Spence Children's Anxiety Scale.