Long COVID Studies
Brief Summary:
ClinicalTrials.gov Identifier NCT06404047
The goal of the study is to find ways to improve the lives of people with exercise intolerance or PEM. With your help, we want to find out if personalized cardiopulmonary rehabilitation (a program to improve your ability to exercise) or structured pacing (a program to help reduce symptoms of PEM) can improve daily functioning. With your help, we can better understand how COVID affects energy levels and find ways to help improve daily functioning for people with Long COVID.
To qualify, you must meet the following inclusion criteria:
If you qualify and choose to join the study, you will receive:
Please contact us to learn more.
Brief Summary:
ClinicalTrials.gov Identifier NCT05595369
This is study evaluates the effect of 15 and 25 days of a drug (Paxlovid) compared to placebo in Long COVID patients with fatigue, brain fog, and autonomic function. Participants will be randomized to study interventions or placebo/controls based on the arms that are actively enrolling at the time of randomization. Study interventions may be added or removed according to adaptive design and/or emerging evidence. When there are multiple study interventions available, randomization will occur based on appropriateness of each intervention for the participant as determined by the study protocol.
To qualify, you must meet the following inclusion criteria:
If you qualify and choose to join the study, you will receive:
Please contact us to learn more.
Brief Summary:
ClinicalTrials.gov Identifier NCT05965752
This study studies the effect of cognitive retraining, goal management, and transcranial stimulation on brain function in Long COVID. This protocol is a prospective, multi-center, multi-arm, randomized, controlled platform trial evaluating potential interventions for PASC-mediated cognitive dysfunction. The hypothesis is that PASC-mediated declines in cognitive domains, such as executive function and attention, may be improved by interventions that selectively focus on enhancing those domains.
To qualify, you must meet the following inclusion criteria:
If you qualify and choose to join the study, you will receive:
Please contact us to learn more.
For Clinical Trial Recruitment