Skaer 1993.
Methods | ‐ Randomised controlled trial ‐ Adequate randomisation ‐ Blinding of patients, administrators and outcome assessors: inadequate ‐ No description of losses to follow‐up ‐ Intention‐to‐treat analysis ‐ Groups were similar at the start of the study ‐ Groups were equally provided of care ‐ Overall judgement of quality: medium | |
Participants | ‐ Single centre study in the USA ‐ 258 Type 2 diabetes patients recruited from primary care services ‐ Participants : intervention I1 (79), I2 (53), I3 (48), control (78) ‐ Sex: I1 (F: 54, M: 25), I2 (F: 31, M:22), I3 (F:29, M: 19), control (F: 49, M: 29) ‐ Mean age: I1 (53.6 yrs, SD 7.7), I2 (51.8 yrs, SD 8.6), I3 (52.3 yrs, SD 8.4), control (51.7 yrs, SD 7.8) ‐ Treatment modality: oral hypoglycaemic agents: I1: 79, I2: 53, I3: 48, control: 78 | |
Interventions | To discern the effect of mailed prescription‐refill reminders (I1), specialised packaging (I2), or a combination of both (I3) on prescription refill compliance and health service utilisation. | |
Outcomes | MPR (medication prescription refill), number of days' supply obtained over 360 days of the trial. | |
Notes | Previously untreated type 2 diabetes patients, prescribed glyburide bd, no utilisation of nurse care for prior 3 months. |