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NCT05119556Active, not recruiting

Video Telehealth Pulmonary Rehabilitation to Reduce Hospital Readmission in Chronic Obstructive Pulmonary Disease

Video Telehealth Pulmonary Rehabilitation to Reduce Hospital Readmission in Chronic Obstructive Pulmonary Disease (Tele-COPD)

Source: ClinicalTrials.gov · Last updated 13 Apr 2026

Brief summary (registry, in English)

The purpose of this study is to compare the efficacy and safety of a real time video telehealth pulmonary rehabilitation intervention with standard of care in patients hospitalized for an exacerbation of chronic obstructive pulmonary disease (COPD) to determine the impact on hospital readmissions and respiratory morbidity, and to investigate the cost-effectiveness of the intervention.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
301 (actual)
First submitted
26 Oct 2021
Start date
28 Jun 2022
Primary completion date
28 Feb 2026
Lead sponsor
University of Alabama at Birmingham
Diseases
COPD
NCT number
NCT05119556

What you commit to

  • Study type: Interventional
  • Participants enrolled: 301
  • From 28 Jun 2022 to the primary completion date, 28 Feb 2026
  • 15 sites 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.

Prior treatment

  • Treatment with chronic or newly initiated home ventilatory support. Those on in-patient short-term non-invasive ventilation will not be excluded.

Other illness

  • Other respiratory conditions that could confound the diagnosis such as asthma, pulmonary fibrosis, bronchiectasis, and lung cancer. Participants with pneumonic exacerbations of COPD will be included.
  • Primary diagnosis of COVID pneumonia. Individuals with incidentally detected COVID or persistently positive for COVID but deemed to be convalescent will not be excluded.
  • Active cancers on chemotherapy or radiation therapy
  • Immunosuppressed states predisposing to frequent hospitalizations including uncontrolled HIV/AIDS
  • Active or recent (within 1 month) myocardial infarction
  • Angina not well-controlled by medication
  • Unstable cardiac arrhythmias, atrial or ventricular
  • Significant cognitive dysfunction, including dementia, that in opinion of investigator would impair ability to safely or effectively engage in study protocol
  • Participants with any terminal medical illnesses as diagnosed by a physician, and/or on hospice

Lab values

  • Secondary diagnosis of congestive heart failure that is severe as documented by active symptoms, New York Heart Association (NYHA) functional classification IV or left ventricular ejection fraction \<25% on echocardiography

Other

  • Supplemental oxygen requirement greater than 5 liters per minute at either rest or with exertion
  • Currently enrolled in and participating in pulmonary rehabilitation
  • Special patient groups such as prisoners and institutionalized patients
  • Participants with musculoskeletal comorbidities or physical infirmities that preclude participation in an exercise program
  • Current participation in any other interventional clinical trial
  • Inability to understand and speak English during exercise sessions
  • Inability or unwillingness to comply with study and/or follow-up procedures outlined in the protocol

Who the study is looking for

  • Age 40 or greater
  • Clinical diagnosis of COPD
  • Hospitalized for acute exacerbation of COPD.
  • Be willing to adhere to trial and follow-up procedures and give informed consent

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

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

SiteCityCountrySite status
Johns Hopkins University
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesUnknown status
HealthPartners Institute
Coordinator of this site? Confirm its status
BloomingtonUnited StatesUnknown status
Boston VA Hospital
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BostonUnited StatesUnknown status
Northern Westchester Hospital/Northwell Health
Coordinator of this site? Confirm its status
ChappaquaUnited StatesUnknown status
Northwestern Memorial Hospital
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ChicagoUnited StatesUnknown status
Cincinnati VA Hospital
Coordinator of this site? Confirm its status
CincinnatiUnited StatesUnknown status
Cleveland Clinic
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ClevelandUnited StatesUnknown status
University of Maryland
Coordinator of this site? Confirm its status
College ParkUnited StatesUnknown status
Baylor College of Medicine
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
University of Iowa
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Iowa CityUnited StatesUnknown status
Minnesota VA HealthCare System
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MinneapolisUnited StatesUnknown status
Temple University Hospital
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
University of Pittsburgh
Coordinator of this site? Confirm its status
PittsburghUnited StatesUnknown status
Wake Forest University
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesUnknown status

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