Zhang 2005.
Methods | RCT | |
Participants | Location: China 94 participants (47 each in control and intervention groups) with clinical diagnosis of stroke according to CCMD‐3 criteria and affective disorders (72 included in final analysis) Intervention group: 64% male, 57.8 years (SD 6.4) Control group: 61% male, 59.2 years (SD 5.8) |
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Interventions | Intervention group: 36 participants, buspirone hydrochloride 20 to 30 mg daily in first week, 40 to 60 mg in second week + routine care Control group: 36 participants, routine care (no description of routine care) Duration: 4 weeks Study dates: May 2001 to June 2002 |
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Outcomes | Anxiety (HAM‐A) and depression (HAM‐D) at 2 and 4 weeks Loss to follow‐up: 22 (11 in each group)
Adverse effects: 5
Other outcomes: American Heart Stroke Outcome Classification |
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Notes | Exclusion: patients with unstable conditions Funding sources/declarations of interest: no details |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | No information provided |
Allocation concealment (selection bias) | Unclear risk | No information provided |
Blinding (performance bias and detection bias) Anxiety | Unclear risk | No information provided |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | High number of losses but balanced between groups |
Selective reporting (reporting bias) | Unclear risk | No information provided |
Other bias | Unclear risk | No information provided |
BI: Barthel Index CCMD‐3: Chinese Classification of Mental Disorders Version 3 CT: computed tomography HADS‐A: Hospital Anxiety and Depression Scale ‐ anxiety subscale HAM‐A: Hamilton Anxiety Scale HAM‐D: Hamilton Depression Rating Scale MRI: magnetic resonance imaging RCT: randomised controlled trial SD: standard deviation SSS: Scandinavian Stroke Scale TICS: Telephone Interview of Cognitive Status