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After obtaining consent from the parents, the first IFSP review was completed after the first IFSP meeting, and the second and the last IFSP review was done toward the end of the data collection, approximately 6 months after the family's entry into early intervention.
After obtaining consent, demographic questionnaires were completed.
After obtaining consent, a study questionnaire was administered.
After obtaining consent, the study questionnaire was administered verbally by a trained study enumerator.
After obtaining consent, enrolled patients were switched to a Servo-i ventilator (Maquet, Solna, Stockholm, Sweden).
After obtaining consent, 420 women were screened and 102 were identified as having anxiety/depression.
After obtaining consent from the subjects, a preliminary study (measurement for one menstrual cycle) was conducted.
After obtaining consent, the treating practitioner performed the standardised elbow extension test (box 2) as part of the examination.
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Interviews were conducted after obtaining signed consent, or verbal consent for those who could not read.
Three healthy volunteers were recruited after obtaining informed consent.
It was a prospective observational study where eligible patients were enrolled after obtaining their consent.
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