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NCT06156202 · ClinicalTrials.gov registry record · NA

Evaluating a Comprehensive Multimodal Outpatient Rehabilitation Program for PASC Program to Improve Functioning of Persons Suffering From Post-COVID-19 Syndrome: A Randomized Controlled Trial

A NA study, sponsored by University of Pennsylvania.

Completed
Registry status
NA
Development phase
125
Enrollment target

NCT06156202: Completed NA study, sponsored by University of Pennsylvania.

NCT06156202 is a NA study that has completed, run by University of Pennsylvania. The registered enrollment target is 125 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06156202, a NA study, has completed, sponsored by University of Pennsylvania.

COMPLETED
Registry status
NA
Development phase
125 participants
Enrollment target

Study Summary

About 10-20% of persons who contract SARS CoV-2 will experience persistent post-acute sequelae of SARSCoV-2 infection (referred here as PASC). While treatments offered at emerging outpatient COVID recovery clinics are being informed by previous similar diseases, the need is great for a better understanding of the unique needs of this growing population and for tested, efficacious rehabilitation programs to address them. We provide both here.The targeted six-week program will be comprised of a core set of therapies, including individually titrated stretching and flexibility, strengthening of accessory breathing muscles and diaphragm, resistance and aerobic conditioning, and vestibular rehabilitation, supplemented by neuropsychological and cognitive remediation tailored to patients' needs.

Interventions

  • OTHER Augmented Usual Care
  • OTHER Comprehensive Rehabilitation

Trial Details

FieldValue
Enrollment Target 125 participants
Start Date 2023-11-15
Est. Completion 2025-11-30
Phase NA

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT06156202

The ClinicalTrials.gov registry entry for NCT06156202 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 125 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Augmented Usual Care is the first listed.

NCT06156202 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06156202 about?

NCT06156202 is a clinical study titled "Evaluating a Comprehensive Multimodal Outpatient Rehabilitation Program for PASC Program to Improve Functioning of Persons Suffering From Post-COVID-19 Syndrome: A Randomized Controlled Trial". About 10-20% of persons who contract SARS CoV-2 will experience persistent post-acute sequelae of SARSCoV-2 infection (referred here as PASC). While treatments offered at emerging outpatient COVID recovery clinics are being informed by previous similar diseases, the need is great for a better unders...

What is the current status of trial NCT06156202?

This trial is currently completed. It is a NA study. The enrollment target is 125 participants. The study started on 2023-11-15. Estimated completion is 2025-11-30.

What interventions are being tested in trial NCT06156202?

The interventions under investigation include: Augmented Usual Care (OTHER), Comprehensive Rehabilitation (OTHER).

Who is sponsoring clinical trial NCT06156202?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.