AI Article Synopsis

  • Several existing COA tools for assessing Sjögren's disease symptoms lack a comprehensive evaluation of health-related quality of life (HRQoL); this study aimed to create a new patient-reported outcome (PRO) instrument for better assessment in clinical settings and trials.
  • The development of the Sjögren's Related Quality of Life (SRQoL) included qualitative interviews with patients to capture their experiences and establish the content validity of the tool and associated severity assessment items (PGI-S and PGI-C).
  • After interviewing 20 participants, eight domains of HRQoL impact were identified, including emotional well-being, sleep, daily activities, cognition, physical functioning, social/family dynamics, work, and sexual functioning, signaling the SRQo

Article Abstract

Introduction: Several clinical outcome assessment (COA) instruments assess Sjögren's disease (Sjögren's) symptoms, but do not provide comprehensive assessment of the health-related quality of life (HRQoL) impact of Sjögren's. This study aimed to develop a patient-reported outcome (PRO) instrument for the assessment of HRQoL, intended for use in clinical trials and clinical practice in the assessment of treatment benefit.

Methods: Review of study sponsor proprietary data and qualitative interviews informed the development of a conceptual model, the Sjögren's Related Quality of Life (SRQoL) and patient global impression of severity (PGI-S) and change (PGI-C) items. Combined concept elicitation and cognitive debriefing interviews with patients with Sjögren's explored their HRQoL impact experience and content validity of the SRQoL and PGI items.

Results: Twenty participants were interviewed about their Sjögren's experience. Following inductive analysis of interviews, concepts were categorized into eight domains: emotional well-being (e.g., worry and stress; n = 20/20; 100%), sleep (e.g., daytime sleepiness and waking up during the night; n = 20/20; 100%), activities of daily living (e.g., difficulty looking at screens and difficulty driving; n = 20/20; 100%), cognition (e.g., concentration difficulties and word finding difficulties; n = 19/20; 95.0%), physical functioning (e.g., difficulty walking and difficulty exercising; n = 19/20; 95.0%), social and family functioning (e.g., dependent on others and relationship difficulties; n = 17/20; 85.0%), work (n = 15/20; 75.0%), and sexual functioning (n = 12/20; 60.0%). SRQoL and PGI items, instructions, response options, and recall period were well understood and relevant to participants.

Conclusions: The SRQoL is a new PRO instrument to assess Sjögren's impact on HRQoL, developed in accordance with regulatory guidance. This study provides considerable insight into the patient experience of Sjögren's and evidence to support the content validity of the SRQoL. Future research should evaluate the psychometric properties of the SRQoL to support its use in clinical trials and clinical practice and further validate its use as an assessment of treatment benefit.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11557853PMC
http://dx.doi.org/10.1007/s40744-024-00718-6DOI Listing

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