Table 1.
Item | Criterion | Study type |
---|---|---|
Study population |
|
|
1 |
Selection before disease was present or at uniform point |
CH/CC/CS |
2 |
Cases and controls were drawn from the same population |
CC |
3 |
Participation rate ≥80% for cases/cohort |
CH/CC/CS |
4 |
Participation rate ≥80% for controls |
CC |
5 |
Sufficient description of baseline characteristics |
CH/CC/CS |
Assessment of risk factor |
|
|
6 |
Psychosocial assessment was blinded |
CH/CC/CS |
7 |
Psychosocial factors were measured identical for cases and controls |
CC |
8 |
Psychosocial factors were assessed prior to the outcome |
CH/CC/CS |
Assessment of outcome |
|
|
9 |
Knee OA/pain was assessed identical in studied population |
CH/CC/CS |
10 |
Presence of knee OA/pain was assessed reproducibly |
CH/CC/CS |
11 |
Presence of knee OA/pain was assessed according to standard definitions |
CH/CC/CS |
Study design |
|
|
12 |
Prospective design was used |
CH/CC/CS |
13 |
Follow up time ≥2 years |
CH |
14 |
Withdrawals ≤20% |
CH |
Analysis and data presentation |
|
|
15 |
Appropriate analysis techniques were used |
CH/CC/CS |
16 | Adjusted for at least age and sex | CH/CC/CS |
CH, Applicable to cohort studies; CC, Applicable to case-control studies; CS, Applicable to cross-sectional studies; OA, Osteoarthritis.