Affiliation:
1. Pôle de Médecine Physique et de Réadaptation UF 4372 Hôpitaux Universitaires de Strasbourg France
2. Service EMOI TC Institut Universitaire de réadaptation Clemenceau Illkirch France
3. Unité INSERM 1114 Neuropsychologie Cognitive et Physiopathologie De La Schizophrénie Strasbourg France
4. Université de Strasbourg Faculté de Médecine Strasbourg France
Abstract
AbstractSingle‐case experimental designs (SCEDs) are a group of methodologies of growing interest, aiming to test the effectiveness of an intervention at the single‐participant level, using a rigorous and prospective methodology. SCEDs may promote flexibility on how we design research protocols and inform clinical decision‐making, especially for personalized outcome measures, inclusion of families with challenging needs, measurement of children's progress in relation to parental implementation of interventions, and focus on personal goals. Design options for SCEDs are discussed in relation to an expected on/off effect of the intervention (e.g. school/environmental adaptation, assistive technology devices) or, alternatively, on an expected carry‐on/maintenance of effects (interventions aiming to develop or restore a function). Randomization in multiple‐baseline designs and ‘power’ calculations are explained. The most frequent reasons for not detecting an intervention effect in SCEDs are also presented, especially in relation to baseline length, trend, and instability. The use of SCEDs on the front and back ends of randomized controlled trials is discussed.What this paper adds
Single‐case experimental designs (SCEDs) may promote flexibility on how we design research protocols.
Randomization in multiple‐baseline designs allows ‘power’ calculations based on randomization tests.
Whenever feasible, N‐of‐1 trials should be preferred to other SCEDs and to group randomized controlled trials.
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Cited by
10 articles.
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