Table S4. Assessment of study design, populations, supplementation and methodological quality.
Study characteristics | n | % |
---|---|---|
Study design† | ||
RCT/qRCT | 13 | 76 |
Single arm | 3 | 18 |
Controlled, other | 1 | 6 |
Randomized trial quality†,‡ | ||
Low risk | 11 | 65 |
Medium risk/unclear | 3 | 18 |
High risk | 3 | 18 |
Age groups§ | ||
Neonates | 4 | 22 |
Infants | 4 | 22 |
Toddlers | 6 | 33 |
Schoolers | 16 | 89 |
Adolescents | 15 | 83 |
Population§ | ||
Healthy/subclinical VDD | 8 | 42 |
Classical diseases | 3 | 16 |
Non-classical diseases | 8 | 42 |
Dosing regimen¶ | ||
Constant | 18 | 64 |
Variable | 10 | 36 |
Dosing groups¶ | ||
RDA/AI-999 | 3 | 11 |
1,000–3,999 | 5 | 18 |
4,000–39,999 | 11 | 39 |
≥40,000 | 9 | 32 |
Frequency¶ | ||
Daily | 18 | 64 |
Intermittent/single dose | 8 | 29 |
Weekly/biweekly | 2 | 7 |
(q)RCT, (Quasi) randomized controlled trial. †, values represent the number of trials, and the percentage out of the 17 identified trials; ‡, studies were assessed using Cochrane risk of bias tool (Higgins & Green, 2008); §, numbers of populations out of 19. For age, numbers will add up to more than 19 populations as some included children from two or more groups; ¶, number of high-dose vitamin D arms out of 28 identified in eligible studies.