Patient-reported outcomes |
N (%) |
1. Examining PROs was a primary objective of the study |
10 (100) |
2. A validated questionnaire to measure PROs was used |
10 (100) |
Study population |
3. The patient sampling process is described |
10 (100) |
4. A (healthy) normative sample is included for comparison |
3 (30) |
5. Patients with both cancer and diabetes are compared to either patients with only cancer or only diabetes on at least two sociodemographic variables |
8 (80) |
6. A description is included of at least two clinical variables regarding cancer diagnosis (e.g., cancer stage, treatment, time since cancer diagnosis) |
8 (80) |
7. A description is included of at least two clinical variables regarding diabetes diagnosis or severity (e.g., HbA1c levels, treatment, time since diabetes diagnosis) |
3 (30) |
8. Inclusion and/or exclusion criteria are described |
9 (90) |
9. Participation rates for patient groups are described and these are >75 % |
4 (40) |
10. Information is given regarding differences in demographic and/or clinical characteristics of respondents vs non-respondents |
3 (30) |
Study design |
|
11. The study sample includes at least 75 patients (arbitrarily chosen) |
8 (80) |
12. The process of data collection is described |
8 (80) |
13. The difference in the outcome variable between cancer patients with diabetes and patients with only cancer and/or only diabetes is assessed in multivariable models, including at least 2 covariates |
8 (80) |
Results |
14. Mean, median, standard deviations, or percentages are reported and compared between cancer patients with diabetes and patients with only cancer and/or only diabetes for the most important outcome measures |
8 (80) |