Li 2013a.

Methods	RCT Method of randomisation: not stated Blinding: not stated Adverse effects: not stated ITT analysis: not stated Losses to FU: not stated
Participants	Country: China Number of participants included: 60 (20/20/20) Demographics: aged 40‐75 years Type of stroke: both ischaemic and haemorrhagic strokes Diagnosis: CT/MRI Severity on entry: not stated Time from stroke onset: 1‐3 months Setting: inpatient Comparability: no significant difference in age or time post onset
Interventions	3 arms: acupuncture only PT only acupuncture + PT Comparison eligible: acupuncture + PT versus PT only Acupuncture treatment Acupuncture rationale: not stated Needling details Points used: body acupoints Numbers of points used: 12 points Depths of insertion: not stated Deqi elicited: not stated Needle stimulation: manual Needle retention time: 30 minute Needle type: not stated Treatment regimen Number of treatment sessions: not stated Frequency of treatment: 7 sessions/week Total course: not stated Practitioner background: not stated Co‐intervention: PT Control interventions: PT
Outcomes	Improvement of motor function (Fugl‐Meyer Assessment) Improvement of pain (Visual Analogue Score) Improvement of independence (ADL) FU: not stated
Notes	‐
Risk of bias
Bias	Authors' judgement	Support for judgement
Random sequence generation (selection bias)	Unclear risk	The method of random sequence generation was not reported
Allocation concealment (selection bias)	Unclear risk	Information on allocation concealment was not reported
Blinding (performance bias and detection bias) All outcomes	Unclear risk	Information on blinding was not reported
Blinding of participants and personnel (performance bias) All outcomes	Unclear risk	Information on blinding was not reported
Blinding of outcome assessment (detection bias) All outcomes	Unclear risk	Information on blinding was not reported
Incomplete outcome data (attrition bias) All outcomes	Unclear risk	Information on attrition was not reported
Selective reporting (reporting bias)	Unclear risk	Free of selective reporting bias was assessed as 'unclear' due to some clinically important outcomes unstated, such as quality of life, mortality and adverse events
Other bias	Unclear risk	No information provided