The document summarizes a randomized clinical trial that evaluated the effect of vitamin D on the severity of dysmenorrhea and menstrual blood loss. The trial involved random assignment of participants to treatment groups, concealed allocation, similar baseline characteristics between groups, blinding of participants, treatment providers, and outcome assessors, identical treatment of groups aside from the intervention, complete follow-up with similar rates between groups, analysis according to randomized groups, consistent measurement of outcomes between groups, reliable outcome measurement, appropriate statistical analysis, and an appropriate trial design with no deviations.
The document summarizes a randomized clinical trial that evaluated the effect of vitamin D on the severity of dysmenorrhea and menstrual blood loss. The trial involved random assignment of participants to treatment groups, concealed allocation, similar baseline characteristics between groups, blinding of participants, treatment providers, and outcome assessors, identical treatment of groups aside from the intervention, complete follow-up with similar rates between groups, analysis according to randomized groups, consistent measurement of outcomes between groups, reliable outcome measurement, appropriate statistical analysis, and an appropriate trial design with no deviations.
The document summarizes a randomized clinical trial that evaluated the effect of vitamin D on the severity of dysmenorrhea and menstrual blood loss. The trial involved random assignment of participants to treatment groups, concealed allocation, similar baseline characteristics between groups, blinding of participants, treatment providers, and outcome assessors, identical treatment of groups aside from the intervention, complete follow-up with similar rates between groups, analysis according to randomized groups, consistent measurement of outcomes between groups, reliable outcome measurement, appropriate statistical analysis, and an appropriate trial design with no deviations.
The document summarizes a randomized clinical trial that evaluated the effect of vitamin D on the severity of dysmenorrhea and menstrual blood loss. The trial involved random assignment of participants to treatment groups, concealed allocation, similar baseline characteristics between groups, blinding of participants, treatment providers, and outcome assessors, identical treatment of groups aside from the intervention, complete follow-up with similar rates between groups, analysis according to randomized groups, consistent measurement of outcomes between groups, reliable outcome measurement, appropriate statistical analysis, and an appropriate trial design with no deviations.
JBI Critical Appraisal Checklist for Randomized Controlled Trials
Title. : The Effect of Vitamin D On the Severity of Dysminorrhea and Menstrual
Blood Loss : a Randomized Clinical Trial Author : Azam Amajerdi Date : 27 Maret 2023 Year : 2023
No Question Yes No Unclear NA
1 Was true randomization used for assignment of participants to V treatment groups? 2 Was allocation to treatment groups concealed? V
3 Were treatment groups similar at the baseline?. V
4 Were participants blind to treatment assignment? V
5 Were those delivering treatment blind to treatment assignment? V
6 Were outcomes assessors blind to treatment assignment? V
7 Were treatment groups treated identically other than the V
intervention of interest? 8 Was follow up complete and if not, were differences between V groups in terms of their follow up adequately described and analyzed? 9 Were participants analyzed in the groups to which they were V randomized? 10 Were outcomes measured in the same way for treatment groups? V 11 Were outcomes measured in a reliable way? V 12 Was appropriate statistical analysis used? V 13 Was the trial design appropriate, and any deviations from the V standard RCT design (individual randomization, parallel groups) accounted for in the conduct and analysis of the trial?