System for Clinical Trial Subject Compliance
7 Assignments
0 Petitions
Accused Products
Abstract
The present invention is designed to develop research protocols for clinical trials. The invention also can track and enhance subject compliance with a research protocol. The invention further provides evaluability data related to subject performance in the clinical trial. According to an alternative embodiment of the invention, a portable electronic device is used to query and collect data from the subject.
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Citations
74 Claims
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1-53. -53. (canceled)
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54. A method of increasing subject compliance during a clinical trial by improving oversight, the method comprising:
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receiving, over a network from a first portable electronic device, first data associated with a first subject of the clinical trial, the first data comprising; first clinical trial data provided by the first subject; and first evaluability data associated with first clinical trial data, the first evaluability data indicating the suitability of the first clinical trial data for use in the clinical trial; receiving, over the network from the first portable electronic device, second data associated with the first subject, the second data comprising; second clinical trial data provided by the first subject after the provision of the first clinical trial data; and second evaluability data associated with the second clinical trial data, the second evaluability data indicating the suitability of the second clinical trial data for use in the clinical trial; generating, by a computer processor, a report providing a graphical display of the first and second evaluability data; communicating the report over the network to one or more of the following recipients; a researcher conducting the clinical trial; and a sponsor of the clinical trial. - View Dependent Claims (55, 56, 57, 58, 59, 60)
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61. A non-transient computer-readable medium comprising instructions operable, when executed by one or more computer processors of a computer system, to cause the computer system to:
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receive, over a network from a first portable electronic device, first data associated with a first subject of the clinical trial, the first data comprising; first clinical trial data provided by the first subject; and first evaluability data associated with first clinical trial data, the first evaluability data indicating the suitability of the first clinical trial data for use in the clinical trial; receive, over the network from the first portable electronic device, second data associated with the first subject, the second data comprising; second clinical trial data provided by the first subject after the provision of the first clinical trial data; and second evaluability data associated with the second clinical trial data, the second evaluability data indicating the suitability of the second clinical trial data for use in the clinical trial; generate a report providing a graphical display of the first and second evaluability data; communicate the report over the network to one or more of the following recipients; a researcher conducting the clinical trial; and a sponsor of the clinical trial. - View Dependent Claims (62, 63, 64, 65, 66, 67)
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68. A system for reporting data related to a clinical trial, the system comprising:
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one or more computer processors; and a non-transient computer-readable medium comprising instructions operable, when executed by the one or more computer processors, to cause the system to; receive, over a network from a first portable electronic device, first data associated with a first subject of the clinical trial, the first data comprising; first clinical trial data provided by the first subject; and first evaluability data associated with first clinical trial data, the first evaluability data indicating the suitability of the first clinical trial data for use in the clinical trial; receive, over the network from the first portable electronic device, second data associated with the first subject, the second data comprising; second clinical trial data provided by the first subject after the provision of the first clinical trial data; and second evaluability data associated with the second clinical trial data, the second evaluability data indicating the suitability of the second clinical trial data for use in the clinical trial; generate a report providing a graphical display of the first and second evaluability data; communicate the report over the network to one or more of the following recipients; a researcher conducting the clinical trial; and a sponsor of the clinical trial. - View Dependent Claims (69, 70, 71, 72, 73, 74)
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Specification