Table 2.
Study design | Clear statement of aims | Rationale for intervention points or adequate baseline measurement | Explanation for lack of control group | Justification for sample choice | Blinded assessment of primary outcome measures | Reliable primary outcome measures | Incomplete outcome data addressed | Intervention unlikely to affect data collection | Attempts to mitigate effects of no control | Analysis sufficiently rigorous | Free of selective outcome reporting | Limitations addressed | Conclusions clear and justified | Free of other bias | Ethics issues addressed | Final ICROMS score | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
de Bruin et al. (2014) | NCBA | + | + | − | + | + | + | + | + | − | + | + | + | + | + | + | 13 |
Note. NCBA = non-controlled before-after; quality ratings: + = yes, − = no,? = unknown; final ICROMS score: low quality = 0–12 points, medium quality = 13–17 points, high quality = 18–26 points.