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Patient assignment to the different populations occurred before the study blind was broken.
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Was the study blinded?
(The study was blinded) and item #24 (The success of blinding was evaluated).
Also, the study is blinded to patient participants, but is not blinded to their healthcare providers.
The study was blinded and prospective.
By its nature, the study precluded blinding.
No study blinded the therapist and few studies blinded the participants.
Only half of the studies tested baseline comparability to ensure that the two groups were equal before wound closure. 1 Similarly, only one study blinded participants and assessors to the method of wound closure by covering the wound with a dressing, in an attempt to limit assessor bias.
The study was single blind and sham-controlled and compared seizure rate in the 7 days before and after tDCS and after sham in a cross-over design.
The study was single blind (participant unaware of product applied).
The study remained double blind.
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