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Study has a population clinically diagnosed with any or a mixture of the following conditions: cerebral infarction, non-traumatic intracerebral haemorrhage.
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Study population solely focuses on any of the following conditions: transient ischaemic attack (TIA), traumatic brain injury, hypoxic brain injury, subarachnoid haemorrhage.
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Study population consists of adult stroke survivors at any period post-clinical diagnosis.
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Study consists of a paediatric stroke population.
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Studies focused on routine clinical practice or care at the micro- and/or meso-levels. (incl. pragmatic studies)
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Studies concentrating on the development of PROs or tools related to the IRPT.
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IRPT at the level of the individual, e.g. shared decision-making between a clinician and patient.
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Studies concentrating on secondary testing or comparative testing of PROs or tools related to the IRPT.
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Interpretation and or feedback of the PROM or tools related to the IRPT necessary.
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Studies concentrating on the psychometric properties of PROs or tools related to the IRPT (e.g. validity and reliability).
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All study designs.
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Studies involving the aggregation of individual scores from PROs or tools related to the IRPT.
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English language or high-quality translation available.
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Studies in which the scores of PROMs or tools related to the IRPT are an outcome of a research study, including the evaluation of an intervention or observational research exploring trends in domains such as quality of life.
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Any secondary research studies including literature reviews, comments, editorials, etc. (this type of study design is reserved for phase 1: theory building. However, secondary sources will be followed for the purpose of discovering further primary sources.)
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Date of publication pre 01/01/00 due to the significant changes to stroke care and services.
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