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Those who are eligible will be consented to the trial by the outcome assessor.
Also, participants will be consented to store biospecimens for future research.
Participants will be consented to the study and then matched in pairs.
Those who are not delirious will be consented to the study and have a MMSE assessment.
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All infants recruited to the TIPIT study[ 37] will be consented separately to have cranial MRI scans at term equivalent.
Those who specialize in lower limb problems and indicate a willingness to participate will receive an information pack and written consent will be consented prior to data collection.
All team members undergoing training will be consented prior to randomisation and the incentive of receiving training at the end of the study is provided to avoid differential levels of dropout or engagement between the two groups of teams.
Patients diagnosed with symptomatic/asymptomatic PHPT will be consented and screened for eligibility to participate in the EPATH trial.
Eligible participants will be consented.
The returned and completed questionnaire will be considered consent to participate in the study.
Previous research suggests that approximately 50% of patients will be willing to consent to completing the questionnaires [ 45].
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