Literature DB >> 32926299

International guidance on the selection of patient-reported outcome measures in clinical trials: a review.

Norah L Crossnohere1, Michael Brundage2, Melanie J Calvert3, Madeleine King4, Bryce B Reeve5, Elissa Thorner6, Albert W Wu7,8, Claire Snyder7,6,8.   

Abstract

PURPOSE: Patient-reported outcomes (PROs) are increasingly used in clinical trials to provide patients' perspectives regarding symptoms, health-related quality of life, and satisfaction with treatments. A range of guidance documents exist for the selection of patient-reported outcome measures (PROMs) in clinical trials, and it is unclear to what extent these documents present consistent recommendations.
METHODS: We conducted a targeted review of publications and regulatory guidance documents that advise on the selection of PROMs for use in clinical trials. A total of seven guidance documents from the US Food and Drug Administration, European Medicines Agency, and scientific consortia from professional societies were included in the final review. Guidance documents were analyzed using a content analysis approach comparing them with minimum standards recommended by the International Society for Quality of Life Research.
RESULTS: Overall there was substantial agreement between guidance regarding the appropriate considerations for PROM selection within a clinical trial. Variations among the guidance primarily related to differences in their format and differences in the perspectives and mandates of their respective organizations. Whereas scientific consortia tended to produce checklist or rating-type guidance, regulatory groups tended to use more narrative-based approaches sometimes supplemented with lists of criteria.
CONCLUSION: The consistency in recommendations suggests an emerging consensus in the field and supports use of any of the major guidance documents available to guide PROM selection for clinical trials without concern of conflicting recommendations. This work represents an important first step in the international PROTEUS Consortium's ongoing efforts to optimize the use of PROs in clinical trials.

Entities:  

Keywords:  Clinical trials; Guidance as topic; Health care; Oncology; Outcome assessment; Quality of life

Year:  2020        PMID: 32926299     DOI: 10.1007/s11136-020-02625-z

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  14 in total

1.  Assessing the meaningful change threshold of Quality of Life in Depression Scale using data from two phase 3 studies of esketamine nasal spray.

Authors:  Heather Rozjabek; Nan Li; Holger Hartmann; Dong Jing Fu; Carla Canuso; Carol Jamieson
Journal:  J Patient Rep Outcomes       Date:  2022-07-10

Review 2.  The health-related quality of life, mental health and mental illnesses of patients with inclusion body myositis (IBM): results of a mixed methods systematic review.

Authors:  Katja C Senn; Laura Gumbert; Simone Thiele; Sabine Krause; Maggie C Walter; Klaus H Nagels
Journal:  Orphanet J Rare Dis       Date:  2022-06-16       Impact factor: 4.303

Review 3.  Assessing Patient-Reported Outcomes in Pediatric Rheumatic Diseases: Considerations and Future Directions.

Authors:  Christina K Zigler; Rachel L Randell; Bryce B Reeve
Journal:  Rheum Dis Clin North Am       Date:  2022-02       Impact factor: 2.032

4.  Optimal outcome measures for assessing exercise and rehabilitation approaches in chemotherapy-induced peripheral-neurotoxicity: Systematic review and consensus expert opinion.

Authors:  Susanna B Park; Stefano Tamburin; Angelo Schenone; Ian R Kleckner; Roser Velasco; Paola Alberti; Grace Kanzawa-Lee; Maryam Lustberg; Susan G Dorsey; Elisa Mantovani; Mehrnaz Hamedani; Andreas A Argyriou; Guido Cavaletti; Ahmet Hoke
Journal:  Expert Rev Neurother       Date:  2022-01-11       Impact factor: 4.287

5.  Could existing infrastructure for using patient-reported outcomes as quality measures also be used for individual care in patients with colorectal cancer?

Authors:  Clara Breidenbach; Christoph Kowalski; Simone Wesselmann; Nora Tabea Sibert
Journal:  BMC Health Serv Res       Date:  2021-05-11       Impact factor: 2.655

6.  The PROTEUS-Trials Consortium: Optimizing the use of patient-reported outcomes in clinical trials.

Authors:  Claire Snyder; Norah Crossnohere; Madeleine King; Bryce B Reeve; Andrew Bottomley; Melanie Calvert; Elissa Thorner; Albert W Wu; Michael Brundage
Journal:  Clin Trials       Date:  2022-01-31       Impact factor: 2.599

7.  Moving Beyond the Momentum: Innovative Approaches to Clinical Trial Implementation.

Authors:  Cathy Eng; Emerson Y Chen; Jane Rogers; Mark Lewis; Jonathan Strosberg; Ramya Thota; Smitha Krishnamurthi; Paul Oberstein; Rang Govindarajan; Gary Buchschacher; Sandip Patel; Davendra Sohal; Taymeyah Al-Toubah; Philip Philip; Arvind Dasari; Hagan Kennecke; Stacey Stein
Journal:  JCO Oncol Pract       Date:  2021-02-03

Review 8.  Patient-Reported Outcomes in Rheumatoid Arthritis: A Key Consideration for Evaluating Biosimilar Uptake?

Authors:  Gabriel Horta-Baas
Journal:  Patient Relat Outcome Meas       Date:  2022-03-30

9.  The role of kidney registries in expediting large-scale collection of patient-reported outcome measures for people with chronic kidney disease.

Authors:  Sabine N van der Veer; Cecile Couchoud; Rachael L Morton
Journal:  Clin Kidney J       Date:  2021-03-16

10.  Patients' Experiences With Staphylococcus aureus and Gram-Negative Bacterial Bloodstream Infections: Results From Cognitive Interviews to Inform Assessment of Health-Related Quality of Life.

Authors:  Heather A King; Sarah B Doernberg; Kiran Grover; Julie Miller; Megan Oakes; Tsai-Wei Wang; Molly McFatrich; Felicia Ruffin; Karen Staman; Hannah G Lane; Abigail Rader; Zoë Sund; Hayden B Bosworth; Bryce B Reeve; Vance G Fowler; Thomas L Holland
Journal:  Open Forum Infect Dis       Date:  2021-12-08       Impact factor: 3.835

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