SBIR-STTR Award

Research Platform Integrating Patient Reported and Clinical Outcomes Data Sources
Award last edited on: 9/20/2013

Sponsored Program
SBIR
Awarding Agency
NIH : NLM
Total Award Amount
$149,512
Award Phase
1
Solicitation Topic Code
879
Principal Investigator
John C Weiss

Company Information

Dynamic Clinical Systems Inc (AKA: DCS)

PO Box 5218
Hanover, NH 03755
   (603) 397-3637
   info@dynamicclinical.com
   www.dynamicclinical.com
Location: Single
Congr. District: 02
County: Grafton

Phase I

Contract Number: 1R43LM011408-01
Start Date: 9/1/2012    Completed: 2/28/2013
Phase I year
2012
Phase I Amount
$149,512
While large, prospective, blinded trials are the gold standard in clinical research, they require significant commitments of resources and time. Further, since these trials seek the answer to rather specific questions, the applicability and scalability of data obtained in these large trials is limited by the way in which it was collected. These trials will likely continue to be the final word in translational research, but in the face o contracting research budgets it is increasingly important to conduct only those studies that have a reasonable likelihood of answering the research hypotheses. Another reality of large, prospective clinical studies is that study designers must make a number of critical decisions (e.g., sample size) before the first data are collected. While statistical analyses exist to estimae sample size, they are often based on incomplete and sometimes insufficient preliminary information. Prior to embarking on an expensive prospective study, it would be particularly advantageous for investigators to have access to a large repository of high quality, codified, de- identified patient data. Given the recent ascension and recognized importance of patient reported outcomes (PRO) data in clinical trials, Dynamic Clinical Systems (DCS) is developing a research platform to open access to its large scale database of clinical PRO data. DCS will provide a unique and innovative solution that enables sustainable data collection and secure data access by opening its Web-based PRO system to researchers. This will provide researchers with access to de-identified PRO data broadly collected during routine care and in clinical studies. Further, DCS will boost the breadth and depth of its PRO data by integrating with complementary data sources and linking longitudinal patient-centric data. The result will be a continuously populating, secure PRO database available to researchers through a user-friendly interface. In Phase I we will 1) integrate our PRO database with a partner database to demonstrate feasibility and 2) create a prototype interface for research access. Feasibility will be established if the integration prototype seamlessly transfers data and passes tree test scenarios. We will test usability by querying clinical researchers as they use the interface prototype.

Public Health Relevance:
Patient-reported outcomes (PRO) measured with sophisticated, yet easy-to-use assessments are a key way in which patients and study participants can communicate with their clinician or study coordinator, respectively. Dynamic Clinical Systems is developing an information technology solution that automates this process so that clinical trials are less expensive, require fewer numbers of participants, are less burdensome, and collect information about the patient's experience from the patient's perspective.

Public Health Relevance Statement:
Patient-reported outcomes (PRO) measured with sophisticated, yet easy-to-use assessments are a key way in which patients and study participants can communicate with their clinician or study coordinator, respectively. Dynamic Clinical Systems is developing an information technology solution that automates this process so that clinical trials are less expensive, require fewer numbers of participants, are less burdensome, and collect information about the patient's experience from the patient's perspective.

NIH Spending Category:
Clinical Research; Clinical Trials

Project Terms:
Address; Area; base; Blinded; Budgets; Clinical; Clinical Data; Clinical Research; Clinical Trials; comparative; Computerized Medical Record; cost; Cost Control; Data; Data Collection; Data Sources; Databases; design; experience; Face; FarGo; Frequencies (time pattern); Genetic Transcription; Goals; Gold; Health; Individual; Information Technology; innovation; large-scale database; Link; Logic; Manuals; Online Systems; Outcome; Outcome Measure; Participant; Patient Outcomes Assessments; Patients; Phase; Phase IV Clinical Trials; Process; prospective; Prospective Studies; prototype; Reporting; repository; Research; Research Contracts; Research Personnel; Resources; routine care; Sample Size; Secure; Site; Solutions; Specific qualifier value; System; Testing; Time; tool; Translational Research; Trees; Update; usability; user-friendly

Phase II

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Start Date: 00/00/00    Completed: 00/00/00
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