NCT06077994Completed
Enhanced Pulmonary Rehabilitation With Digital Remote Home Monitoring
The Enhanced Pulmonary Rehabilitation Program With Digital Remote Patient Monitoring: A Feasibility Randomized Clinical Trial
Source: ClinicalTrials.gov · Last updated 8 Sept 2025
Brief summary (registry, in English)
The primary objective of the current randomized controlled trial is to assess feasibility of integrating digital remote patient monitoring (dRPM) with the an enhanced Breathe Easy Pulmonary Rehabilitation Program for Individuals with COPD and Comorbidities (BEPR+), including aspects such as recruitment, retention, patient adherence, technology acceptability, adverse events, and staffing resources. The secondary objectives include comparing clinical outcomes (such as functional capacity, health status, quality of life, self-management, psychosocial health, physical activity and self-efficacy) between those who receive dRPM and BEPR+ (dRPM+) vs. those who receive BEPR+ alone.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 78 (actual)
- First submitted
- 28 Sept 2023
- Start date
- 28 Sept 2023
- Primary completion date
- 1 Aug 2024
- Lead sponsor
- University of Alberta
- Diseases
- COPD
- NCT number
- NCT06077994
What you commit to
- Study type: Interventional
- Participants enrolled: 78
- From 28 Sept 2023 to the primary completion date, 1 Aug 2024
- 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
- As part of standard rehabilitation referral procedures, all patients must be ambulatory and not have unstable cardiovascular disease.
Other
- Patients with cognitive impairments who are unable to accurately complete questionnaires will also be excluded.
Who the study is looking for
- patients must be enrolled into pulmonary rehabilitation at the G.F. MacDonald Centre for Lung Health with a diagnosis of chronic lung disease (COPD confirmed by post-bronchodilator forced expiratory volume in 1 second by forced vital capacity (FEV1/FVC) ratio of less than 0.7).
- Patients must be able to read and communicate in English and willing and able to use digital devices.
Age in the registry: 30 years to 100 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| G. F. MacDonald Centre for Lung Health Coordinator of this site? Confirm its status | Edmonton | Canada | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.