Alanzi 2018.
Study characteristics | ||
Methods |
Evaluation of the effectiveness of mobile diabetes management system with social networking and cognitive behavioural therapy (CBT) for T2D RCT (NA clusters and NA providers), conducted in 1) All participants were from a clinic in Saudi Arabia‐Damman. 2) Mobile diabetes management system operated remotely through the SANAD system. Figure 1 shows that diabetic nurses and CBT therapists were involved in the delivery of the intervention. In Saudi Arabia. 2 arms: 1) Control (conventional diabetes treatment) (control arm) and 2) Intervention (SANAD system) (intervention arm) |
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Participants | Control arm N: 10 Intervention arm N: 10, NA, NA Diabetes type: 2 Mean age: NR ± 6.45 % Male: 75 Longest follow‐up: 6 months |
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Interventions |
Control arm: (conventional diabetes treatment) Intervention arm: (SANAD system) 1) Electronic patient registry 2) Patient education |
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Outcomes | 1) Glycated haemoglobin | |
Funding source | No information of funding source. "Some of the limitations of this study that may affect internal and external validity include the small sample size (n = 20), which was due to limited funding" | |
Notes | — | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not reported |
Allocation concealment (selection bias) | Unclear risk | Not reported. |
Patient's baseline characteristics (selection bias) | Low risk | See Table 1, education lower in control group, but all other characteristics balanced. |
Patient's baseline outcomes (selection bias) | Low risk | Table 1) Baseline HbA1c P value > 0.05 |
Incomplete outcome data (attrition bias) | Low risk | 1 patient lost in the intervention group (1/10 or 10%). None lost in the control group. |
Blinding of participants and personnel (performance bias) and of outcome assessors (detection bias) | Low risk | Objective measure for HbA1c. |
Selective reporting (reporting bias) | Unclear risk | No registered protocol. Methods match outcomes. |
Risk of contamination (other bias) | Unclear risk | Patient randomised. Both groups were monitored by the same staff. Unlikely that the control group received the SANAD intervention. |
Other bias | Low risk | No evidence of other bias. |