Evidence map›Paper›PMID 42436453›Full record

ArticleBMC infectious diseases2026

Symptom variation up to two years post-SARS-CoV-2 infection in Children and Young People: results from the Children and young people with Long Covid (CLoCk) study.

Natalia K Rojas, Roz Shafran, Terence Stephenson, Alvin Richards-Belle, Esther Ortega-Martin, Emma Dalrymple, Isobel Heyman, Fiona Newlands, Kelsey McOwat, Ruth Simmons and 1 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Natalia K RojasDivision of Surgery & Interventional Science, Faculty of Medical Sciences, University College London, London, WC1E 6BT, UK. n.rojas@ucl.ac.uk.ORCID http://orcid.org/0000-0002-6615-9618
Roz ShafranUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Terence StephensonUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Alvin Richards-BelleUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Esther Ortega-MartinDepartment of General Economy (Sociology), Faculty of Nursing and Physiotherapy, University of Cadiz, Cadiz, 11009, Spain.
Emma DalrympleUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Isobel HeymanUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Fiona NewlandsUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Kelsey McOwatImmunisation Department, UK Health Security Agency, 61 Colindale Avenue, London, NW9 5EQ, UK.
Ruth SimmonsImmunisation Department, UK Health Security Agency, 61 Colindale Avenue, London, NW9 5EQ, UK.
Snehal M Pinto PereiraDivision of Surgery & Interventional Science, Faculty of Medical Sciences, University College London, London, WC1E 6BT, UK. snehal.pereira@ucl.ac.uk.ORCID http://orcid.org/0000-0002-0876-8757

Funding

Beryl Alexander Charity 183885Medical Research Council MR/Y009398/1National Institute for Health and Care Research COV-LT-0022
6 · The paper itself

Abstract

backgroundPost Covid-19 Condition (PCC) can fluctuate over time, yet, no in-depth investigation of the heterogeneous PCC trajectories that can exist in children and young people (CYP) has been undertaken. We aim to examine associations between PCC trajectories in CYP over 2-years following infection and (i) factors prior to the COVID-19 pandemic/infection including socio-demographic variables (e.g., age, sex, ethnicity), health and educational needs status and (ii) factors subsequent to infection including the nature, number, functional impact and severity of symptoms, as well as mental health and wellbeing.

methods943 PCR-test positive CYP (enrolled January-March 2021) were followed-up over two-years (till January-March 2023). Five PCC trajectory groups were specified: (i) chronic, (ii) recovered, (iii) fluctuating, (iv) late onset and (v) never PCC. These groups were compared in terms of factors at baseline using multinomial logistic regression and concurrent health during the two-year period using Chi-Square/Fisher's Exact tests.

resultsBaseline factors prior to the pandemic/infection such as female sex, older age, poorer pre-infection mental and physical health, prior healthcare use, and educational needs were strongly and consistently associated with adverse PCC trajectories. Compared to those aged 11-to-14-years at infection, those aged 15-to-17-years had a 2.44 (95%CI:1.39,4.26) higher risk of being in the chronic group (compared to the never group). Similarly, the risk of being in the fluctuating group was 1.57 (95%CI:1.04,2.37), the recovered group was 2.08 (95%CI:1.10,3.92) and the late-onset group was 1.50 (95%CI:1.08,2.07). Other sociodemographic factors, such as ethnicity and region of residence, had more modest and inconsistent associations. PCC trajectories differed by concurrent number, frequency, functional impact and severity of symptoms and mental health. CYP with chronic PCC consistently reported a higher median number of symptoms (5+) compared to the other groups (median symptoms ≤ 3). Mental health and wellbeing, of the chronic PCC group was also consistently worse (e.g., 41% of the chronic group consistently were classified as 'cases' on the Strengths and Difficulties scale vs 17%-to-2% of the other groups).

conclusionsThere were consistent differences between PCC trajectories, in terms of sex, age, pre-infection mental and physical health, healthcare use, and educational needs. Understanding factors associated with PCC trajectory heterogeneity in CYP and how these trajectories differ over time can help with treatment planning.

Indexed as

COVID-19AdolescentChildChild, PreschoolFemaleHumansMaleMental HealthPost-Acute COVID-19 SyndromeSARS-CoV-2Young AdultChildren and Young PeopleCohort studyCOVID-19Long COVIDMental healthPost Covid-19 condition

Identifiers

PMID42436453
PMCPMC13640280

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.