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Baseline assessments were blinded (collected pre-randomisation) and measured by two assessors who also supervised the training sessions.
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Examiners were blinded to previously collected data.
20 All data were collected blinded to final outcome measures.
However, the interviewers were not blinded when they collected data.
Weight and height were measured and recorded at each visit by a trained technician blinded to previously collected data.
Anthropometric measurements, family history, cancer staging, and other clinical, pathologic, and tumour molecular data were prospectively collected, blinded to patient outcome.
A researcher blinded to allocation collected primary outcome data at the final trial visit; non-attendees were sent the questionnaires by post.
The clinical examinations were performed at each school by a single examiner, who was blinded to previous collected data at that moment, under natural light with the adolescent sitting in school chair, leaning his/her head back, following the international criteria standardized by the World Health Organization for research in oral health [ 15].
However, all clinical and echocardiographic data were collected blinded to each other and to BNP values, preventing an artificially high correlation between the LCA and both cardiac abnormalities and the biomarker, due to the subjective and observer-dependent nature of the items being assessed.
Symptom data, expectations, and beliefs concerning blinding were collected at baseline, 3, and 6 weeks.
The same blind observer collected the patient satisfaction level in the post-operative period.
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CEO of Professional Science Editing for Scientists @ prosciediting.com