Chan 2012.
Methods | Randomisation by random sequences on black paper Single‐blind (participants blinded): outcome assessors blinded |
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Participants | 1 centre in Hong Kong 87 participants with neurogenic dysphagia with similar baseline characteristics 60 (69%) participants with dysphagia due to cerebral infarct < 6 months; other causes of neurogenic dysphagia include intracranial haemorrhage, vascular dementia, Parkinson's disease Clinical evidence of dysphagia |
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Interventions | All groups given routine swallowing therapy Rx 1: true acupuncture (n = 20) Rx 2: sham acupuncture that did not puncture true acupoints lying on a meridian (n = 19) C: routine swallowing therapy only (n = 48) Treatment for up to 4 weeks |
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Outcomes | Outcomes: Royal Brisbane Hospital Outcome Measure Scale (RBHOMS), swallow function by consistencies of ingested food and fluid | |
Notes | Exclusions: structural oral, pharyngeal, or oesophageal disease; severe primary disease of the liver, kidneys, hematopoietic system, or endocrine system; malignant tumour or infectious disease; inability to follow commands Follow‐up: 3 months | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Randomisation by random sequences |
Allocation concealment (selection bias) | Low risk | Allocation concealed in opaque envelopes |
Blinding (performance bias and detection bias) All outcomes | Low risk | Single (participants) blinded |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Single (participants) blinded |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Outcome assessors blinded |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No losses to follow‐up reported |
Selective reporting (reporting bias) | Low risk | All outcomes reported |
Other bias | Low risk | None identified |