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Updated: Jun 17, 2025

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Designing and optimizing clinical trials for long COVID
Julia Moore Vogel1, Beth Pollack2, Ezra Spier3
1Scripps Research Translational Institute, Scripps Research, La Jolla, CA, United States of America; Patient-Led Research Collaborative, United States of America.
Abstract:
Long COVID is a debilitating, multisystemic illness following a SARS-CoV-2 infection whose duration may be indefinite. Over four years into the pandemic, little knowledge has been generated from clinical trials. We analyzed the information available on ClinicalTrials.gov, and found that the rigor and focus of trials vary widely, and that the majority test non-pharmacological interventions with insufficient evidence. We highlight promising trials underway, and encourage the proliferation of clinical trials for treating Long COVID and other infection-associated chronic conditions and illnesses (IACCIs). We recommend several guidelines for Long COVID trials: First, pharmaceutical trials with potentially curative, primary interventions should be prioritized, and both drug repurposing and new drug development should be pursued. Second, study designs should be both rigorous and accessible, e.g., triple-blinded randomized trials that can be conducted remotely, without participants needing to leave their homes. Third, studies should have multiple illness comparator cohorts for IACCIs such as myalgic encephalomyelitis (ME/CFS) and dysautonomia, and screen for the full spectrum of symptomatology and pathologies of these illnesses. Fourth, studies should consider inclusion/exclusion criteria with an eye towards equity and breadth of representation, including participants of all races, ethnicities, and genders most impacted by COVID-19, and including all levels of illness severity. Fifth, involving patient-researchers in all aspects of studies brings immensely valuable perspectives that will increase the impact of trials. We also encourage the development of efficient clinical trial designs including methods to study several therapies in parallel.
Insights
Clinical trials for Long COVID are insufficient, often focusing on unproven non-drug treatments. Prioritizing pharmaceutical interventions and rigorous, accessible study designs is crucial for understanding and treating this chronic condition.
Area of Science:
- Infectious Diseases
- Clinical Trials
- Chronic Illness Research
Background:
- Long COVID, a multisystemic illness post-SARS-CoV-2 infection, lacks sufficient clinical trial data over four years into the pandemic.
- Existing clinical trials for Long COVID exhibit variable rigor and focus, with a majority testing non-pharmacological interventions lacking robust evidence.
Purpose of the Study:
- To analyze the landscape of Long COVID clinical trials.
- To identify shortcomings in current research methodologies.
- To propose guidelines for improving future Long COVID and infection-associated chronic conditions and illnesses (IACCIs) clinical trials.
Main Methods:
- Analysis of data from ClinicalTrials.gov regarding Long COVID and IACCIs trials.
- Review of existing trial designs, interventions, and methodologies.
- Formulation of recommendations based on identified gaps and promising ongoing trials.
Main Results:
- The majority of current Long COVID trials test non-pharmacological interventions with insufficient evidence.
- Significant variability exists in the rigor and focus of ongoing clinical trials.
- Promising trials are underway, but a broader and more rigorous approach is needed.
Conclusions:
- Pharmaceutical trials with potentially curative interventions, including drug repurposing and new development, should be prioritized for Long COVID.
- Rigorous, accessible study designs (e.g., remote triple-blinded randomized trials) and inclusion of comparator cohorts for related IACCIs are recommended.
- Equity in inclusion/exclusion criteria and the integration of patient-researchers are vital for impactful Long COVID research.
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