Table 1.
Table of included studies
Participant characteristics |
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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.