Initial Content Validation and Roadmap for a New Patient-Reported Outcome Measure of Pain Intensity.


Journal

The journal of pain
ISSN: 1528-8447
Titre abrégé: J Pain
Pays: United States
ID NLM: 100898657

Informations de publication

Date de publication:
11 2022
Historique:
received: 07 04 2022
revised: 09 06 2022
accepted: 11 07 2022
pubmed: 23 7 2022
medline: 9 11 2022
entrez: 22 7 2022
Statut: ppublish

Résumé

Measures of pain intensity (eg, numeric rating scales [NRS]) are widely used in clinical research and practice. While these measures have evidence for validity and reliability, poor standardization of instructions, and response options limits precision of pain assessment, allows for inconsistency in interpretation, and presents a challenge for comparison and aggregation of study results. Despite these pitfalls, the 0 to 10 NRS remains the most commonly used primary outcome measure in clinical trials of pain treatments and is the core measure recommended by regulatory agencies. The purpose of this study was to describe the first phase in the development of a pain intensity measure that is easily interpretable, psychometrically sound, and that adheres to FDA qualification processes. The Analgesic, Anesthetic, and Addiction Clinical Trial, Translations, Innovations, Opportunities, and Networks (ACTTION) public-private partnership conducted concept elicitation interviews (N = 44; 22 with acute pain; 22 with chronic pain) to understand the patient perspective on rating pain intensity and to identify actionable suggestions for improved clarity and meaningfulness of instructions, recall periods, and response options. This article summarizes interview findings, describes how patient input and FDA feedback informed preliminary candidate measures, and provides an overview of the FDA qualification process. PERSPECTIVE: Concept elicitation interviews informed the development of content-valid candidate measures of acute and chronic pain intensity for planned use in clinical trials of pain treatments, and comprise the initial stage in FDA clinical outcome assessment qualification. Measures will subsequently be evaluated through cognitive interviews and a series of psychometric studies.

Identifiants

pubmed: 35868594
pii: S1526-5900(22)00360-1
doi: 10.1016/j.jpain.2022.07.001
pii:
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S. Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1945-1957

Informations de copyright

Copyright © 2022 United States Association for the Study of Pain, Inc. Published by Elsevier Inc. All rights reserved.

Auteurs

Dale J Langford (DJ)

Department of Anesthesiology, Critical Care and Pain Management, Hospital for Special Surgery, New York, NY. Electronic address: langfordd@hss.edu.

Jennifer S Gewandter (JS)

Department of Anesthesiology and Perioperative Medicine, University of Rochester, Rochester, NY.

Dagmar Amtmann (D)

Department of Rehabilitation Medicine, University of Washington, Seattle, WA.

Bryce B Reeve (BB)

Department of Population Health Sciences, Center for Health Measurement, Duke University, Durham, NC.

Amy Corneli (A)

Department of Population Health Sciences, Center for Health Measurement, Duke University, Durham, NC.

Kevin McKenna (K)

Department of Population Health Sciences, Center for Health Measurement, Duke University, Durham, NC.

Teresa Swezey (T)

Department of Population Health Sciences, Duke University, Durham, NC.

Molly McFatrich (M)

Department of Population Health Sciences, Center for Health Measurement, Duke University, Durham, NC.

Mark P Jensen (MP)

Department of Rehabilitation Medicine, University of Washington, Seattle, WA.

Dennis C Turk (DC)

Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA.

Robert H Dworkin (RH)

Department of Anesthesiology and Perioperative Medicine, University of Rochester, Rochester, NY.

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