COVID-19 Clinical Trial
Official title:
TARGet Kids! COVID-19 Study of Children and Families
NCT number | NCT04449978 |
Other study ID # | 1000069701 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | April 9, 2020 |
Est. completion date | December 31, 2022 |
The novel coronavirus (COVID-19) was declared a global pandemic in March 2020. Early research suggests that children are no more susceptible to COVID-19 infection than adults and that children with confirmed COVID-19 have generally presented with milder symptoms. However, the impact of COVID-19 among Canadian children remains unclear. The prevalence of COVID-19 in children in Canada is currently unknown and no published research exists regarding the risk factors of COVID-19 in children or its potential long-term health effects on physical health or development. Using TARGet Kids!, Canada's largest children's cohort study with over 11,000 children involved, the researchers will conduct a longitudinal observational study aimed to evaluate the cumulative incidence of COVID-19 in children and parents; differences among infected and uninfected children in terms of age, sex, and income; risk factors of COVID-19; and longer term health effects of COVID-19 among children. Given the rapid spread of COVID-19 and the unknown health effects of the virus in children, research must be conducted to determine the extent of infections of COVID-19 in children, disease severity, risk factors for infection, and how the virus affects children as they become older.
Status | Recruiting |
Enrollment | 1082 |
Est. completion date | December 31, 2022 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A to 16 Years |
Eligibility | Inclusion Criteria: - Families with existing participants of the TARGet Kids! cohort with children between the ages of 0-16 years. Exclusion Criteria: - Families who are not participating in the TARGet Kids! cohort or participating families with no children within the age of eligibility. |
Country | Name | City | State |
---|---|---|---|
Canada | St Michael's Hospital | Toronto | Ontario |
Canada | The Hospital for Sick Children | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
The Hospital for Sick Children | Unity Health Toronto |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cumulative Incidence of COVID-19 | To evaluate the cumulative incidence of laboratory-confirmed COVID-19 among healthy children and parents in Toronto, Canada | 12 months | |
Secondary | Risk Factors for COVID-19 | To determine the risk factors for COVID-19 infection in children and parents to inform preventive interventions | 12 months | |
Secondary | Parent-reported probable case definition of COVID-19 | To determine the cumulative incidence of parent-reported probable case definition of COVID-19 among children and parents. | 12 months | |
Secondary | Dynamics of COVID-19 | To determine the dynamics of COVID-19 infection using a susceptible-infected-recovered (SIR) multi-state model. | 12 months | |
Secondary | Risk to family members | To determine the risk to family members with a laboratory-confirmed COVID-19 infected family member. | 12 months | |
Secondary | Severity of COVID-19 | To determine the severity of laboratory-confirmed COVID-19 in healthy children and parents | 12 months | |
Secondary | Longer term effects of COVID-19 on physical health | To determine the longer term effects of COVID-19 infection in healthy children and parents on physical health | 12 months | |
Secondary | Longer term effects of COVID-19 on mental health | To determine the longer term effects of COVID-19 infection in healthy children and parents on mental health | 12 months | |
Secondary | Longer term effects of COVID-19 on child development | To determine the longer term effects of COVID-19 infection in healthy children and parents on child development | 12 months | |
Secondary | Longer term effects of COVID-19 on family functioning | To determine the longer term effects of COVID-19 infection in healthy children and parents on family functioning | 12 months | |
Secondary | Longer term effects of COVID-19 on health behaviours | To determine the longer term effects of COVID-19 infection in healthy children and parents on health behaviours | 12 months | |
Secondary | Longer term effects of COVID-19 on healthcare utilization | To determine the longer term effects of COVID-19 infection in healthy children and parents on healthcare utilization | 12 months | |
Secondary | Effects of preventive measures on infection | To determine the effect of preventive measures on COVID-19 infection | 12 months | |
Secondary | Effects of preventive measures on physical health | To determine the effect of preventive measures on physical health | 12 months | |
Secondary | Effects of preventive measures on mental health | To determine the effect of preventive measures on mental health | 12 months | |
Secondary | Effects of preventive measures on child development | To determine the effect of preventive measures on child development | 12 months | |
Secondary | Effects of preventive measures on family functioning | To determine the effect of preventive measures on family functioning | 12 months | |
Secondary | Effects of preventive measures on health behaviours | To determine the effect of preventive measures on health behaviours | 12 months | |
Secondary | Effects of preventive measures on healthcare utilization | To determine the effect of preventive measures on healthcare utilization | 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT06065033 -
Exercise Interventions in Post-acute Sequelae of Covid-19
|
N/A | |
Completed |
NCT06267534 -
Mindfulness-based Mobile Applications Program
|
N/A | |
Completed |
NCT05047601 -
A Study of a Potential Oral Treatment to Prevent COVID-19 in Adults Who Are Exposed to Household Member(s) With a Confirmed Symptomatic COVID-19 Infection
|
Phase 2/Phase 3 | |
Recruiting |
NCT05323760 -
Functional Capacity in Patients Post Mild COVID-19
|
N/A | |
Recruiting |
NCT04481633 -
Efficacy of Pre-exposure Treatment With Hydroxy-Chloroquine on the Risk and Severity of COVID-19 Infection
|
N/A | |
Completed |
NCT04537949 -
A Trial Investigating the Safety and Effects of One BNT162 Vaccine Against COVID-19 in Healthy Adults
|
Phase 1/Phase 2 | |
Completed |
NCT04612972 -
Efficacy, Safety and Immunogenicity of Inactivated SARS-CoV-2 Vaccines (Vero Cell) to Prevent COVID-19 in Healthy Adult Population In Peru Healthy Adult Population In Peru
|
Phase 3 | |
Recruiting |
NCT05494424 -
Cognitive Rehabilitation in Post-COVID-19 Condition
|
N/A | |
Active, not recruiting |
NCT06039449 -
A Study to Investigate the Prevention of COVID-19 withVYD222 in Adults With Immune Compromise and in Participants Aged 12 Years or Older Who Are at Risk of Exposure to SARS-CoV-2
|
Phase 3 | |
Enrolling by invitation |
NCT05589376 -
You and Me Healthy
|
||
Completed |
NCT05158816 -
Extracorporal Membrane Oxygenation for Critically Ill Patients With COVID-19
|
||
Recruiting |
NCT04341506 -
Non-contact ECG Sensor System for COVID19
|
||
Completed |
NCT04512079 -
FREEDOM COVID-19 Anticoagulation Strategy
|
Phase 4 | |
Completed |
NCT04384445 -
Zofin (Organicell Flow) for Patients With COVID-19
|
Phase 1/Phase 2 | |
Completed |
NCT05975060 -
A Study to Evaluate the Safety and Immunogenicity of an (Omicron Subvariant) COVID-19 Vaccine Booster Dose in Previously Vaccinated Participants and Unvaccinated Participants.
|
Phase 2/Phase 3 | |
Active, not recruiting |
NCT05542862 -
Booster Study of SpikoGen COVID-19 Vaccine
|
Phase 3 | |
Withdrawn |
NCT05621967 -
Phonation Therapy to Improve Symptoms and Lung Physiology in Patients Referred for Pulmonary Rehabilitation
|
N/A | |
Terminated |
NCT05487040 -
A Study to Measure the Amount of Study Medicine in Blood in Adult Participants With COVID-19 and Severe Kidney Disease
|
Phase 1 | |
Terminated |
NCT04498273 -
COVID-19 Positive Outpatient Thrombosis Prevention in Adults Aged 40-80
|
Phase 3 | |
Active, not recruiting |
NCT06033560 -
The Effect of Non-invasive Respiratory Support on Outcome and Its Risks in Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-COV-2)-Related Hypoxemic Respiratory Failure
|