2015
DOI: 10.1111/acps.12448
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Efficacy of a Danish version of the Cool Kids program: a randomized wait‐list controlled trial

Abstract: The study contributes to the evidence base for the Cool Kids program, previously only evaluated by its developers in Australia. Generic group CBT programs may not be the most appropriate treatment for children and adolescents with primary SoP.

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Cited by 51 publications
(61 citation statements)
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References 40 publications
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“…Sensitivity to treatment effects: Significant effect for treatment versus wait list control or treatment as usual for SCAS‐C and SCAS‐P (Arendt, Thastum, & Hougaard, ; Cobham, ; Wuthrich et al., ). SCAS‐C (Barrett, Farrell, Ollendick, & Dadds, ); Child but not parent effects (van Starrenburg, Kuijpers, Kleinjan, Hutschemaekers, & Engels, ).…”
Section: Evidence‐based Measures/psychometric Criteria – What Do We Lmentioning
confidence: 99%
“…Sensitivity to treatment effects: Significant effect for treatment versus wait list control or treatment as usual for SCAS‐C and SCAS‐P (Arendt, Thastum, & Hougaard, ; Cobham, ; Wuthrich et al., ). SCAS‐C (Barrett, Farrell, Ollendick, & Dadds, ); Child but not parent effects (van Starrenburg, Kuijpers, Kleinjan, Hutschemaekers, & Engels, ).…”
Section: Evidence‐based Measures/psychometric Criteria – What Do We Lmentioning
confidence: 99%
“…The ADIS-C/P has previously proven to be a reliable instrument for assessing anxiety disorder symptoms and diagnoses based on the DSM-IV, with good to excellent test-retest reliability (26). In the RCT study used as the PT group benchmark, an interrater reliability check of the Danish version of ADIS-C/P was conducted by two trained assessors watching and rating 22 (20.2%) of the videorecorded baseline interviews (24). The interrater reliability (Cohen's κ) for the primary anxiety diagnosis was 0.77.…”
Section: Primary Outcome Measurementioning
confidence: 99%
“…The education, procedure, and supervision of the assessors in the ST group were identical to the assessors in the PT study. No interrater reliability check was conducted for the ST group (24).…”
Section: Primary Outcome Measurementioning
confidence: 99%
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“…2) Precision: We lowered SOE one or two levels based on the confidence intervals and sample size. If confidence intervals included appreciable benefits and harms (crossing no effect), or the total sample size was lower than 400 (an arbitrary cutoff that corresponds to a standardized small effect of 0.20 with significance of 0.05 and power of 0.80), 30 we rated SOE down by one level. When both of these situations were encountered simultaneously, we rated SOE down twice for imprecision and labeled this scenario as "severe imprecision".…”
Section: Grading the Strength Of Evidencementioning
confidence: 99%