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Active, not recruiting No phase listed Observational Accepts healthy volunteers

Understanding the Long-term Impact of COVID on Children and Families

ClinicalTrials.gov ID: NCT05172011

Public ClinicalTrials.gov record NCT05172011. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 12:03 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

NIH RECOVER: A Multi-site Observational Study of Post-acute Sequalae of SARS-CoV-2 Infection in Children

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a combined retrospective and prospective, longitudinal, observational meta-cohort of individuals age 0-25 years who will enter the cohort with and without SARS-CoV-2 infection at varying stages before and after infection. Individuals with and without SARS-CoV-2 infection and with or without PASC symptoms will be followed to identify risk factors and occurrence of PASC. This study will be conducted in the United States and participants will be recruited through inpatient, outpatient, and community-based settings. Study data including age, demographics, social determinants of health, medical history, vaccination history, details of acute SARS-CoV-2 infection, overall health and physical function, and PASC symptoms will be reported by participants or collected from the electronic health record using a case report form at specified intervals. Biologic specimens will be collected at specified intervals, with some tests performed in local clinical laboratories and others performed by centralized research centers or banked in the Biospecimen Repository. Advanced clinical examinations and radiologic examinations will be performed at local study sites with cross-site standardization.

Study identification

NCT ID
NCT05172011
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
NYU Langone Health
Other
Enrollment
15,028 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
Up to 25 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 1, 2022 (Actual)
Primary completion
Apr 1, 2027 (Estimated)
Completion
May 23, 2027 (Estimated)
Last update posted
Dec 31, 2025

2022 – 2027

United States locations

U.S. sites
65
U.S. states
33
U.S. cities
54
Facility City State ZIP Site status
University of Alabama at Birmingham (Pregnancy Cohort) Birmingham Alabama 35294 —
Arkansas Children's Hospital and Research Institute Little Rock Arkansas 72202 —
University of California San Diego La Jolla California 92093 —
Children's Hospital Los Angeles Los Angeles California 90027 —
University of California San Diego Health - Rady Children's Hospital San Diego California 92123 —
University of California San Francisco (Pregnancy Cohort) San Francisco California 94115 —
University of California San Francisco San Francisco California 94143 —
Connecticut Children's Medical Center Hartford Connecticut 06106 —
Yale School of Medicine (YSM) New Haven Connecticut 06510 —
ChristianaCare Health System Newark Delaware 19718 —
Nemours Children's Health Wilmington Delaware 19803 —
George Washington University Washington D.C. District of Columbia 20052 —
Kapi'olani Medical Center for Women & Children Honolulu Hawaii 96826 —
Northwestern University Evanston Illinois 60208 —
Northshore University HealthSystem Glenview Illinois 60026 —
American Academy of Pediatrics Itasca Illinois 60143 —
American Academy of Family Physicians Leawood Kansas 66211 —
University of Louisville - Norton Children's Hospital Louisville Kentucky 40202 —
Louisiana State University (LSU) - Pennington Biomedical Research Center Baton Rouge Louisiana 70808 —
Tulane University New Orleans Louisiana 70118 —
Johns Hopkins University Baltimore Maryland 21218 —
Mass General Brigham - Harvard University Boston Massachusetts 02114 —
Harvard Medical School Boston Massachusetts 02115 —
Harvard School Of Public Health Boston Massachusetts 02115 —
Northeastern University Boston Massachusetts 02115 —
Central Michigan University - College of Medicine Detroit Michigan 48201 —
Mayo Clinic Rochester Minnesota 55905 —
University Of Nebraska Medical Center Omaha Nebraska 68198 —
Dartmouth-Hitchcock Lebanon New Hampshire 03766 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Rutgers University New Brunswick New Jersey 08901 —
Saint Peter's University Hospital New Brunswick New Jersey 08901 —
The Pediatric Specialty Center at Saint Barnabas West Orange New Jersey 07052 —
University of New Mexico Health Sciences Center Albuquerque New Mexico 87102 —
NYU Langone Health New York New York 10016 —
Columbia University New York New York 10027 —
Columbia University (Pregnancy) New York New York 10032 —
NewYork-Presbyterian Hospital Queens New York 11355 —
New York Medical College Valhalla New York 10595 —
University of North Carolina (UNC) at Chapel Hill Chapel Hill North Carolina 27516 —
Duke University Medical Center Durham North Carolina 27710 —
WakeMed Health & Hospitals Raleigh North Carolina 27610 —
Good Samaritan Hospital Cincinnati Ohio 45220 —
University Hospitals MacDonald's Women's Hospital Cleveland Ohio 44106 —
Metrohealth System Cleveland Ohio 44109 —
The MetroHealth System (Pregnancy Cohort) Cleveland Ohio 44109 —
The Ohio State University - Wexner Medical Center Columbus Ohio 43210 —
Miami Valley Hospital Dayton Ohio 45409 —
Children's Mercy Hospital Fairfield Ohio 45014 —
University of Oklahoma Health Sciences Center (OUHSC) Oklahoma City Oklahoma 73104 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
University of Pittsburgh Medical Center (UPMC) Pittsburgh Pennsylvania 15213 —
Rhode Island Hospital Providence Rhode Island 02903 —
Women & Infants Hospital Providence Rhode Island 02905 —
Medical University of South Carolina (MUSC) Charleston South Carolina 29425 —
Prisma Health Upstate Greenville South Carolina 29605 —
Avera Research Institute Sioux Falls South Dakota 57108 —
University of Texas Medical Branch (UTMB) Galveston Galveston Texas 77555 —
University of Texas Health Science Center at Houston Houston Texas 77024 —
Baylor College of Medicine Houston Texas 77030 —
University of Utah Health Salt Lake City Utah 84132 —
University of Vermont (UVM) Children's Hospital Burlington Vermont 05401 —
Virginia Commonwealth University Richmond Virginia 23284 —
West Virginia University Morgantown West Virginia 26506 —
Medical College Of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05172011, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 31, 2025 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05172011 live on ClinicalTrials.gov.

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