# Post-COVID Condition Does Not Alter Cognitive Functions in Young Adults: A Cross-Sectional Study in North India

**Authors:** Vatsal A Batra, Kairavi B Unarkat, Manpreet Kaur, Himani Ahluwalia, Soumen Manna

PMC · DOI: 10.7759/cureus.82208 · Cureus · 2025-04-13

## TL;DR

A study in North India found that young adults who had mild COVID-19 infection did not show cognitive impairments months later.

## Contribution

This study is one of the first to assess long-term cognitive effects of mild COVID-19 in young adults using standardized tools.

## Key findings

- No significant cognitive deficits were observed in young adults post-mild COVID-19.
- Cognitive domains like memory, attention, and processing speed were comparable to healthy controls.

## Abstract

Background

Long COVID, or post-COVID condition, includes multi-system chronic sequelae that can last weeks, months, or even years in some individuals after recovery from COVID-19 infection. Prominent among these long-term sequelae are cognitive deficits that may prove to be problematic, especially for the working young adult population. The present study aimed to determine whether cognitive deficits are observed long after recovery from mild COVID-19 infection.

Methods

In this cross-sectional observational study, 29 young adult undergraduate medical students with a history of mild COVID-19 infection at least two years prior were included as cases, while 29 age- and sex-matched undergraduate medical students with no history of COVID-19 were recruited as controls. Sociodemographic data were collected, and the participants were then administered a series of cognitive tests using the National Institutes of Health (NIH) Toolbox V3 software (Toolbox Assessments Inc., Chicago, USA; https://nihtoolbox.org/) to evaluate the cognitive functions, including executive function, cognitive flexibility, attention, working and episodic memory, and processing speed.

Results

The mean age of the cases and controls was 19.37 ± 0.92 and 19.65 ± 0.99 years, respectively. However,there was no statistically significant difference in cognitive function performance across any of the tested domains between cases and controls.

Conclusion

The results of our study indicate that, compared to healthy controls, cognitive functions were not impaired in young adults who previously had symptomatic mild COVID-19 infection.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** vascular damage (MESH:D057772), insomnia (MESH:D007319), cognitive deficits (MESH:D003072), Deficits in memory, attention span (MESH:D001289), Post-COVID Condition (MESH:D000094024), fatigue (MESH:D005221), cognitive symptom (MESH:D019954), neurological deficits (MESH:D009461), impairment of auditory working memory (MESH:D008569), dyspnea (MESH:D004417), Fluid (MESH:D002559), PCOS (MESH:D011085), neurological disease (MESH:D020271), brain injuries (MESH:D001930), neurological impairment (MESH:D009422), myalgia (MESH:D063806), anxiety (MESH:D001007), impairment of attention of visual working memory (MESH:D014786), COVID-19 (MESH:D000086382), tissue damage (MESH:D017695), respiratory failure (MESH:D012131), inflammation (MESH:D007249), neuroinflammation (MESH:D000090862), depressed mood (MESH:D003866), joint pain (MESH:D018771), infection (MESH:D007239), impairment of neurological functions (MESH:D003291), palpitation (MESH:D006331), sleep-related problems (MESH:D020183)
- **Chemicals:** lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12079157/full.md

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Source: https://tomesphere.com/paper/PMC12079157