Long-Term Look at Long COVID after COVID-19
Official title: Longitudinal Study of Patients With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Post-Acute Sequelae of COVID-19 (PASC)
Run by University of North Carolina, Chapel Hill · NCT07781501 · Data updated 2026-11-12
Researchers will see how common Long COVID is and how symptoms stick around over time in adults who had COVID-19, using questionnaires and saliva samples to look for biological clues.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | University of North Carolina, Chapel Hill Academic / other |
| Locations | 1 site (Chapel Hill, North Carolina) |
| Status | Recruiting |
| Started | September 4, 2024 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2029 |
| Registry record updated | September 28, 2026 |
| Trial ID | NCT07781501 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–75 with a prior laboratory-confirmed SARS-CoV-2 infection who can consent and complete study procedures.
✕Probably not a fit
Participants without persistent symptoms or who do not carry the identified risk factors may receive no direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study follows people with a past SARS-CoV-2 infection to measure how often Long COVID symptoms occur, how severe they are, and how they persist. Participants provide health information through surveys and give saliva samples for analysis of proteins, metabolites, microbes, and immune markers. Machine learning will combine demographic, clinical, symptom, and saliva data to identify patterns that predict persistent symptoms. The study aims to uncover factors that contribute to Long COVID and improve prediction of who is at higher risk. Enrollment includes adults aged 18–75, both new participants and those with prior involvement.
Why it matters
Potential benefit: Findings could help doctors predict who is at risk for persistent symptoms and guide future care for Long COVID.
How similar studies have gone: Other observational studies have shown value in linking symptoms with biological markers, though predictive models for Long COVID are still being refined.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18 to 75 years. * Previous laboratory-confirmed SARS-CoV-2 infection. * Willing and able to provide informed consent. * Able to complete study questionnaires and study procedures. Exclusion Criteria: * Current severe periodontal disease with bleeding gums. * Current oral herpes flare, aphthous ulcer, or oral candidiasis (thrush). * Oral viral or bacterial infection within the previous 30 days. * Dry mouth that would prevent adequate saliva collection. * Active alcohol or drug abuse. * Medical or genetic syndrome or developmental delay that would prevent completion of study procedures or questionnaires.
Where it's running
-
University of North Carolina
Chapel Hill, North Carolina, United States Recruiting
Study contacts
- Principal investigator: Laura Jacox, PhD, DMD, MS — University of North Carolina, Chapel Hill
- Study coordinator: Laura A Jacox, PhD, DMD, MS
- Email: ljacox@live.unc.edu
- Phone: +1 847-702-0988
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.