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Participants in this study are 38 learners of Spanish at The University of Hong Kong who were registered in sub-groups of intact classes of the course SPAN2001-Spanish II (corresponding to a level of Spanish B1 or lower-intermediate), who agreed to participate in such a study and, consequently, signed the corresponding consent form.
This request is sent to the CMS which extracts the patient and loads the corresponding consent document from the repository using the transaction Retrieve Document Set (ITI-43).
The participants in this study completed the scale after sign the corresponding consent, adjusted to the Code of Practice for Research at the University of Valladolid (Spain, last update of the Governing Council of 31 January 2013).
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Data indicate the percentage of respondents who assigned the indicated rank to the corresponding consenting option.
With a corresponding consent form, the patient authorises the study guidance to ask for an alignment of study data with information (if existing) from the Cancer Registry of Rhineland-Palatinate on her/his cancer status, giving permission for the use of personal data.
Parents/guardians of preschoolers were then provided with a letter of information detailing the study, along with a corresponding consent form to sign if interested in participating in the study.
Human tumour samples were obtained with the corresponding written consent given by the patients.
All accepted to participate in the study providing the corresponding verbal consent.
All participating patients agreed to take part in the research project through the corresponding informed consent process.
To verify the model, radiological images (X-rays) were taken over a group of 25 healthy, male individuals with average age of 27.4 and average weight of 78.6 kg with the corresponding informed consent.
The study subjects were Caucasians, ≥ 40 and ≤ 90 years of age at the time of inclusion in the FRIDEX cohort, understood and spoke the Spanish language, were able to respond to the initial and/or follow up telephone questionnaire (TQ) and accepted to participate in the study providing the corresponding informed consent.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com