Li 2014.
Methods | Randomisation via minimisation software Single‐blind ‐ assessors blinded No significant differences in baseline comparability tests in all groups of participants |
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Participants | Recruitment through newspaper advertisements and flyers in China 118 participants with dysphagia and hemispheric stroke |
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Interventions | Rx 1: neuromuscular electrical stimulation (VitalStim) Rx 2: combined NMES and traditional swallowing therapy C: traditional swallowing therapy (Data from Rx 2 vs control used in this review) |
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Outcomes | Swallow score, oral transit time, pharyngeal transit time, laryngeal closure duration, PAS | |
Notes | Exclusion: progressive stroke, other neurological disease, neoplastic disease, previous surgery to swallowing apparatus, nasogastric tube | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer randomisation via minimisation software |
Allocation concealment (selection bias) | Low risk | Allocation concealed by sealed envelope |
Blinding (performance bias and detection bias) All outcomes | Low risk | Outcome assessor blinded |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Participants and technicians not blinded |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | As above |
Incomplete outcome data (attrition bias) All outcomes | High risk | 17 participant dropouts |
Selective reporting (reporting bias) | Low risk | All outcomes reported |
Other bias | Low risk | None identified |