Author Webinar: Patient-Reported Outcomes Assessments - Spotlight on the Quality of Life Disease Impact Scale (QDIS®)
- This event has passed.
Quality of Life Disease Impact Scale (QDIS®)
Missed the live webinar?
REGISTER HERE to watch the recording
A new approach to improving patient-reported disease-specific quality of life measures: shorter, more clinically valid and standardized across conditions
Dr John E. Ware, Founder and Chief Science Officer at John Ware Research Group (JWRG) and developer of the SF-36® Health Survey, will present the new Quality of Life Disease Impact Scale (QDIS®), a family of disease specific QOL impact forms with content expanded to be as comprehensive as the best generic QOL surveys in terms of domain representation. QDIS forms differ from generic surveys by using disease-specific attributions proven to increase validity and responsiveness in relation to disease severity or change in severity of a specific disease or condition. QDIS is the first such survey with content and scoring standardized across chronic conditions and normed in the US chronically ill population (mean=50, SD=10) to enable norm-based interpretation.
Because QOL impact scores are standardized across multiple chronic conditions (MCC), QDIS output also includes the first individualized disease specific QOL impact profile and the first aggregate multiple chronic conditions (MCC) total QOL impact score.
JWRG are pleased to announce that the non-profit Mapi Research Trust (MRT) will manage and distribute their licenses to use QDIS survey forms worldwide.
What you will learn:
- Observe historical trends in the content and scoring of widely used patient-reported outcome (PRO) measures;
- Appreciate what makes disease-specific and generic (general) QOL measures different and their practical implications;
- Become familiar with the psychometric methods of QDIS construction that are the basis of a summary score and use of more practical computerized adaptive test (CAT) methods.
- Understand how QDIS content and metrics were standardized across general population and in disease-specific applications and how alternate QDIS forms satisfy their different requirements.
- Review empirical evidence demonstrating gains in validity, including responsiveness, using QDIS in comparison with legacy generic and disease-specific measures.
- Become informed regarding practical aspects of QDIS dissemination by Mapi Research Trust for scholarly and commercial purposes.
This webinar will appeal to all healthcare professionals, clinical researchers and pharmaceutical companies interested in patient-Reported Outcomes (PROs) and Quality of Life (QOL).
John E. Ware, Jr., PhD
Dr. Ware, Chief Science Officer at John Ware Research Group, Research Professor in the Department of Medicine, Tufts University School of Medicine and Visiting Professor in the College of Health Solutions, Arizona State University, is an internationally recognized expert in patient-reported outcomes (PRO) and an elected member of the National Academy of Medicine (formerly Institute of Medicine). He led the development of the outcome measures used in the RAND Health Insurance Experiment, served as the Principal Investigator for the Medical Outcomes Study where he developed the SF-36® Health Survey, and led International Quality of Life Assessment Project translations of the SF-36 for use in multinational clinical trials and population health surveys, which have grown to more than 150 languages. In the 1990’s, Dr. Ware was among the first to apply “modern” psychometric methods and computerized adaptive testing (CAT) to generic and disease-specific measures to cross-calibrate medical care outcomes and population health and estimate scores more efficiently. He founded QualityMetric to develop web-based PROs and served as its CEO and CSO for 10 years. Dr. Ware has published more than 450 peer-reviewed articles on the accuracy and validity of PROs in capturing medical care outcomes and PROs as among the best predictors of the costs of healthcare, job loss and mortality. His current work focuses on the integration of disease-specific and generic PROs using improved adaptive survey logic to make patient screening and outcomes monitoring more practical and more useful in clinical research and practice.
Marie-Pierre Emery, MSc
Marie-Pierre Emery has been working in the field of Patient-Reported Outcomes (PRO) and Clinical Outcome Assessments (COA) within the non-profit Mapi Research Trust for over 25 years. Leading a team of 25 people in her positions of Operations Director and Associate Director of Mapi Research Trust, she developed and contributed to the success of all PRO and COA information activities at Mapi Research Trust, including the creation of online databases of PRO and COA instruments (PROQOLID), of PRO and COA claims granted by Health Authorities in the US and Europe (PROLABELS), PRO and COA information searches and targeted literature reviews, and the management and international distribution of over 500 PROs and COAs and their derivatives such as translations and electronic versions, on behalf of their authors and copyright holders. Beside human resources and team management (recruitment / integration / annual performance evaluation), her responsibilities also covered finances / budget, organization, business development, strategy, marketing / communication, project management, continuous improvement of resources and processes, and quality assurance.
Today, Marie-Pierre uses her 25-year experience and her privileged relationship with numerous actors in the fields of PROs and COAs, to establish collaborative agreements with authors and copyright holders of instruments and contribute to the centralization, dissemination and exponential use of PROs and COAs in clinical research and practice worldwide, for the ultimate benefit of the Patients.