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In addition to the stated purpose of the sample collection, we identified the scope of the consent that was being requested.
The consent being requested is (i) to take part in the intervention and (ii) to provide follow up data in 3 and 12 months time for the longitudinal study (even if they are not willing to take part in the intervention); b) Control group: Consent to take part in the trial will not be sought from men randomised into the control group as they need to remain unaware of the trial (see Ethics, below).
If they were not able to consent, surrogate consent was requested from their families.
The 1999 survey was considered program evaluation and written consent was not required; verbal consent was requested from all participants (health workers and children's caretakers).
Consent should be requested on a regular basis.
For mothers/fathers under the age of 18 years, assent will be obtained and informed consent will be requested from their parent, guardian or spouse/partner over the age of 18 years.
Also signed consent forms were requested from all participants.
If the patient is eligible for inclusion and agrees to participate, informed consent will be requested.
If patients are willing and eligible to participate, written informed consent will be requested.
Oral consent was requested within 48 hours and a written consent within 96 hours.
Since treating students under the age of 16 differently by requesting parental consent might have represented an obstacle to the adolescents, no parental consent was requested.
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CEO of Professional Science Editing for Scientists @ prosciediting.com