Smith 2011.
Methods | Design: cluster‐RT Groups: intervention group (goal setting for allergic rhinitis); control group (standard pharmacy care) |
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Participants | Pharmacies: 20 (8 intervention; 12 control) Pharmacy workers: 38 (22 clinicians; 16 non‐clinicians) ‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐ Pharmacy user: 150 patients with intermittent allergic rhinitis (IAR) (77 intervention; 77 control)
Setting: urban Country: Australia |
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Interventions |
Pharmacy worker‐directed intervention: workshop covering the pathophysiology of allergic rhinitis (AR), the current 'Allergic Rhinitis and its Impact on Asthma' (ARIA) guidelines and pharmacotherapy relating to specific AR symptoms. Also training in self‐management theory, goal setting and up‐skilling in patient counselling
Pharmacy worker control: only received the workshop covering the pathophysiology of AR, the current ARIA guidelines and pharmacotherapy relating to specific AR symptoms. ‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐ Pharmacy user‐directed intervention: patients received an informational brochure and received a goals card titled ‘‘My Goals and Treatment Card’’ where two goals were stated: ‘‘Eliminate/minimise hay fever symptoms’’ and ‘‘Avoid/minimise hay fever triggers’’ to record what they experienced. Individually tailored strategies were developed from these data collaboratively between the participant and the pharmacist or assistant, and entered onto the goals card.
Pharmacy user control: usual treatment and a take‐home brochure on AR at follow‐up visit |
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Outcomes |
Pharmacy worker: not assessed ‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐‐ Pharmacy user:
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Notes | Study/intervention name: Pharmacy Allergic Rhinitis Intervention Study (PARIS) Funding source: funded by the Australian Government Department of Health and Ageing as part of the Fourth Community Pharmacy Agreement Research & Development Program managed by the Pharmacy Guild of Australia |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Randomised, but method not specified |
Allocation concealment (selection bias) | Unclear risk | Randomised, but method not specified |
Baseline outcome measures similar | Low risk | No significant differences between groups |
Baseline characteristics similar | Low risk | No significant differences between groups |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | No information reported |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No information on blinding |
Protection against contamination | Low risk | Randomisation by pharmacists |
Selective reporting (reporting bias) | Low risk | All outcomes reported |
Other bias | Unclear risk | Only a small group of pharmacies |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Presumably pharmacy workers knew grouping |