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Individual data will be monitored by study investigators on completion of testing and during the intervention.
Fall diary data will be monitored by using data transfer to a secure server.
Errors and missing data will be monitored during data-collection, and complemented or corrected whenever possible.
Data will be monitored for completeness and quality by the Clinical Trials Research Unit.
The accuracy, completeness and progress of data will be monitored continuously throughout the trial.
All data will be monitored by study personnel during regular monitoring visits.
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The study progress, safety data and data quality will be monitored by an Independent Data (and safety) Monitoring Board (IDMB), which will be independent of the trial organizers.
Trial data integrity will be monitored by regularly checking data files for omissions and errors.
Trial data integrity will be monitored by regularly scrutinising data files for omissions and errors.
These data safety will be monitored at the National Center for Cardiovascular Diseases of the People's Republic of China during the clinical trial.
Data collection procedures will be monitored and source data verification against the paper data collection forms undertaken at regular intervals.
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