Table 3. Methodological quality of included studies.
Barlow et al.(2010) | Constantino & Bricker (1996) | Constantino et al. (2001) | De Groot et al. (2010) | Farberow (1992) | Kovac & Range (2000) | Wittouck et. al (2014) | |
---|---|---|---|---|---|---|---|
Selection Bias | Weak | Weak | Weak | Weak | Weak | Moderate | Weak |
Representative? | Not likely | Not likely | Not likely | Somewhat likely | Not likely | Somewhat likely | Not likely |
Percentage agreement1 | 60–79% | 80–100% | Can`t tell | Less than 60% | Can`t tell | 60–79% | 80–100% |
Study Design | Moderate | Strong | Strong | Weak | Moderate | Strong | Strong |
Study Design | Cohort (one group pre and post) | RCT | RCT | Secondary analyses of an RCT | Cohort analytic (two groups pre and post) | Controlled Clinical trial | RCT |
Described as randomized? | No | Yes | Yes | Yes | No | Yes | Yes |
Method of randomization described? | N.A. | Yes | Yes | Yes2 | N.A. | No | Yes |
Method appropriate? | N.A. | Yes | Yes | Yes | N.A. | N.A. | Yes |
Confounders | N.A. | Strong | Strong | Strong | Weak | Weak | Strong |
Important pre-intervention differences? | No | No | Yes | Yes | Yes | Yes | |
Percentage confounders controlled for? | N.A | N.A | 0–100% | Less than 60% | Less than 60% | 80–100% | |
Blinding | Weak | Weak | Weak | Weak | Weak | Strong | Weak |
Outcome assessor described as blinded? | No | No | No | No | No | Yes | No |
Participants blinded? | No | Can`t tell | Can`t tell | Can`t tell | Can`t tell | Yes | Can`t tell |
Data Collection Method | Strong | Weak | Weak | Strong | Weak | Weak | Strong |
Measures valid? | Yes | Can`t tell | Can`t tell | Yes | No | No | Yes |
Measures reliable? | Yes | Yes | Yes | Yes | No | Yes | Yes |
Withdrawals and Dropouts | Weak | Strong | Moderate | Strong | Weak | Moderate | Strong |
Number and reasons reported per group? | No | Can`t tell | No | Yes | Can`t tell | Yes | Yes |
Percentage completing study? | Less than 60% | 80–100% | 60–79% | 80–100% | Can`t tell | Less than 60% | 80–100% |
Number of strong ratings | 1/6 | 3/6 | 2/6 | 4/6 | 0/6 | 2/6 | 4/6 |
Intention-to-treat analysis | No | No | Can`t tell | Yes | Yes | No | No |
1 Refers to the % of subjects in the control and intervention group that agreed to participate in the study before they were assigned to intervention or control group.
2 described in De Groot et al. (2007), RCT = randomized controlled trial