Ryff‐de Lèche 1992.
Study characteristics | ||
Methods |
Clinical application of two computerized diabetes management systems: comparison with the log‐book method Cross‐over RCT, conducted in an outpatient clinic at University Hospital of Basel, Switzerland Two arms: 1. Group 2 ‐ Log book control (control arm) and 2. Group 1 ‐ Camit‐S1 analysis program (intervention arm) |
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Participants | Control arm N: 9 Intervention arm N: 10 Diabetes type: type 1 Median age: 52.0 (range: 21 to 60) % Male: 68.4 Longest follow‐up: 3 months |
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Interventions |
Control arm: 1) Facilitated relay of clinical information 2) Promotion of self‐management Intervention arm: 1) Facilitated relay of clinical information 2) Promotion of self‐management |
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Outcomes | 1) HbA1c, mean % (SE) Control arm: pre 7.0 (0.2), post 6.7 (0.3) Intervention arm: pre 6.8 (0.3), post 6.3 (0.3) |
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Funding source | This work was supported by a grant of Boehringer Manheim Switzerland | |
Notes | — | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Information not available. |
Allocation concealment (selection bias) | Unclear risk | Information not available. |
Patient's baseline characteristics (selection bias) | Unclear risk | Information not available. |
Patient's baseline outcomes (selection bias) | Low risk | Information not available. |
Incomplete outcome data (attrition bias) | Low risk | Information not available. |
Blinding of participants and personnel (performance bias) and of outcome assessors (detection bias) | Low risk | Information not available. |
Selective reporting (reporting bias) | Low risk | Information not available. |
Risk of contamination (other bias) | Unclear risk | This needs discussion. |
Other bias | Unclear risk | Information not available. |