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NCT06156202Completed

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

Evaluating a Comprehensive Multimodal Outpatient Rehabilitation Program to Improve the Functioning of Persons Suffering From Post-acute Sequelae of SARS-CoV-2 Infection (PASC): A Randomized Controlled

Source: ClinicalTrials.gov · Last updated 20 Jan 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
125 (actual)
First submitted
28 Nov 2023
Start date
15 Nov 2023
Primary completion date
30 Nov 2025
Lead sponsor
University of Pennsylvania
NCT number
NCT06156202

What you commit to

  • Study type: Interventional
  • Participants enrolled: 125
  • From 15 Nov 2023 to the primary completion date, 30 Nov 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Severe cognitive impairment (i.e. Alzheimer's, Dementia)

Other

  • Participation in another clinical trial
  • Score greater than 12 on the fatigue scale
  • Score greater than 30 on the memory/thinking scale
  • Mental or physical inability to participate in the program

Who the study is looking for

  • 18 years if age or older
  • English or Spanish speaking
  • Previously tested positive for COVID
  • Still having symptoms not explained by any other etiologies
  • Cognitive impairment
  • Fatigue

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital of the University of Pennsylvania
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.