Hogg 2008
| Methods | Purpose: to compare a comprehensive preventive intervention programme to no intervention Design: cluster‐RCT, match‐paired; "The unit of randomization and analysis was the practice; the unit of observation was the patient." Duration of study: 11.5 months Interval between intervention and when outcome was measured: "The intervention lasted 11.5 months." "Data were collected ... up to 2 months after the intervention." Power computation: 24 practices were needed to detect a mean difference of 0.07 in the primary outcome between intervention and control groups ("The delta selected (0.07) approximates the 10% change in care frequently associated with care improvement interventions"), SD = 0.083, α = 0.05, β = 0.83, and 27 practices were recruited to allow for 15% attrition Statistics: Chi2, paired t‐tests | |
| Participants | Country: Canada Setting: 2 letters and brochure to 351 primary care practices in eastern Ontario; 54 practices participated Eligible participants: (health status): ≥ 65 Age: ≥ 65 Gender: not stated | |
| Interventions | Intervention 1: comprehensive preventive intervention programme; facilitators were assigned 13 to 14 practices and visited them monthly, average duration of visit 46 minutes; facilitators encouraged 26 preventive manoeuvres; with baseline audit, feedback and consensus building, and periodic follow‐up and consensus building Control: no intervention | |
| Outcomes | Outcome measured: % influenza vaccination for each practice Time points from the study that are considered in the review or measured or reported in the study: "The intervention lasted 11.5 months." "Data were collected ... up to 2 months after the intervention." % vaccinated by: "up to 2 months after the intervention" | |
| Notes | Funding: Canadian Institutes of Health Research | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | Practices were matched on solo versus group practice, presence of nursing staff and location (rural or urban) and each pair member was randomly assigned using the Statistical Analysis software package." |
| Allocation concealment (selection bias) | Low risk | "The allocation sequence was kept locked and unavailable to the administrative staff until the time of assignment." |
| Blinding (performance bias and detection bias) All outcomes | Low risk | "Physicians and facilitators were blinded to the actual manoeuvres that would be included in the preventive performance index." |
| Incomplete outcome data (attrition bias) All outcomes | Low risk | 54 practices randomised, data from 54 analysed (27 intervention, 27 control practices) |
| Selective reporting (reporting bias) | Low risk | No selective reporting |