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Because one target can yield hundreds or thousands of incidental sub-targets — people connected to the target whose call records will be requested and stored — it's possible that 2017's targets just had fatter, longer contact lists and deeper networks than 2016's.
In case of declaration of a health event, medical records will be requested (hospitalization, diagnosis, etc).
Linked records will be requested from the following data sources for members of the study population (figure 1).
The women will be asked to complete a questionnaire and data from the medical records will be requested regarding the delivery.
All MBS records will be requested for children in the study population from birth until the end of their first year of school.
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Inclusion and exclusion criteria will be verified in the hospital clinical record, and written informed consent will be requested from the patient.
However, a record of any additional rehabilitation input (type of input and number of additional appointments) together with a record of any other investigations/interventions will be requested as part of the 3-month, 6-month and 12-month follow-ups, and this will also form part of the trial data set.
Following the 12-week intervention, the participants will be requested to record their weekly training to investigate the long-term compliance.
All women will be requested to record use of resources (number and type of health care contacts, medication use, adjunct treatments) during the trial period and the effect of these treatments.
The participants in the group allocated to the MEDIC-treatment will be requested to record their weekly exercise until the long-term follow-up 2 years after randomisation to investigate the long-term compliance.
Subjects will be requested to formally record the type and amount of treatment they receive.
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CEO of Professional Science Editing for Scientists @ prosciediting.com