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Within-person variability and the minimal important difference of the EQ-VAS in adults with post-COVID-19 condition: a secondary analysis of data from a single-centre randomised controlled trial

In brief

Researchers estimate an 8-point meaningful change on long COVID health ratings

In 153 adults with post-COVID-19 condition, researchers estimated that an 8-point change on the 0-to-100 health rating scale represents a meaningful difference. Ratings varied considerably from day to day, supporting weekly averages over single-day scores; the estimate comes from a fatigue-predominant group, so its relevance to other people with long COVID remains uncertain.

Journal
BMJ open (Q1)
Published
25 September 2026
Study design
Randomized controlled trial
Evidence level
Level 1, High (CEBM 1b)
Authors
Julia Kopp, Tala Ballouz, Dominik Menges, Anja Frei, Julia Braun, Lisa Kuenzi, et al.
PMID
42790915
DOI
10.1136/bmjopen-2026-121051

Why clinicians should know about it

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Abstract

OBJECTIVE: To describe the distribution and day-to-day variability of EuroQol Visual Analogue Scale (EQ-VAS) values and to estimate a minimal important difference (MID) in adults with post-COVID-19 condition (PCC). DESIGN: Secondary analysis of pooled EQ-VAS data from both arms of a 12-week randomised, placebo-controlled trial (PYCNOVID) of Pycnogenol (200 mg/day) versus placebo in adults with PCC. SETTING: Single centre study in Switzerland between June 2023 and July 2024. PARTICIPANTS: Adults with PCC with at least one of the following symptoms: fatigue, post-exertional malaise, dyspnoea or brain fog. MAIN OUTCOME MEASURE: EQ-VAS ratings over 7 consecutive days before baseline (randomisation) and at follow-up (after 12 weeks). Weekly mean EQ-VAS values and within-person SDs (wpSD) were calculated. The MID was estimated using distribution-based and anchor-based methods with prespecified correlation criteria, using the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) instrument as the primary anchor, along with additional anchors. RESULTS: Among 153 participants, baseline EQ-VAS values were low, with a median of 48.7 on a 0-100 scale. Day-to-day variability was considerable, with a median wpSD of 6.4. Distribution-based MID estimates ranged from 5.9 to 8.9 points. FACIT-Fatigue was the only anchor meeting the correlation threshold (ρ≥0.30), yielding an anchor-based MID of 8.96 points. Triangulation of these estimates supported a final MID estimate of 8 EQ-VAS points. CONCLUSIONS: Adults with PCC reported markedly impaired and highly variable health status. Weekly aggregation of daily EQ-VAS ratings likely provides a more robust estimate than single-day assessments. A PCC-specific EQ-VAS MID of 8 points, derived from a chronic, fatigue-predominant PCC population, facilitates interpretation of meaningful change and improves outcome definition and sample size planning in future studies. Applicability to earlier-stage or non-fatigue-predominant PCC populations warrants further investigation. TRIAL REGISTRATION NUMBER: NCT05890534.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.