NCT06822179CompletedPhase 2
Effectiveness of a Personalized In-home Telerehabilitation Program on Self-Care in Patients With Long COVID
Effectiveness of a Personalized In-home Telerehabilitation Program on Self-Care in Patients With Long COVID: A Randomized Clinical Trial
Source: ClinicalTrials.gov · Last updated 8 Oct 2026
Brief summary (registry, in English)
The goal of this clinical trial is to evaluate whether a 12-week tele-rehabilitation programme roduces medium-term improvements in self-management, fatigue and quality of life in patients affected by persistent COVID. The main questions it aims to answer are: * Will a multimodal program (exercise with education) improve the self-management ability of patients with post-exertional malaise? * Does fatigue and quality of life will be improved in these patients? Researchers will compare an experimental breath program to a control standard care group to see if multimodal program works to treat post-exertion malaise. Participants will: -Follow-up 12 weeks online sessions: 1 weekly synchronous online session (Exercise and education) + educational resources
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 57 (actual)
- First submitted
- 11 Feb 2025
- Start date
- 1 Mar 2025
- Primary completion date
- 1 Jun 2026
- Lead sponsor
- CEU San Pablo University
- Diseases
- Long COVID and ME/CFS
- NCT number
- NCT06822179
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 57
- From 1 Mar 2025 to the primary completion date, 1 Jun 2026
- 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.
Prior treatment
- Patients with a history of respiratory or cardiovascular diseases prior to COVID-19, other acute or chronic diseases that may interfere with the study
Other
- Pregnancy/breastfeeding
- Those with contraindications to respiratory muscle training.
Who the study is looking for
- Post COVID-19 condition: individuals with a history of probable or confirmed SARS-CoV-2 infection, usually 3 months from the onset of COVID-19 with symptoms that last for at least 2 months and cannot be explained by an alternative diagnosis. Common symptoms include fatigue, shortness of breath, cognitive dysfunction
- Between 18 and 75 years of age
- Possibility of access and use of smartphone.
- Ability to attend the clinic in person for an initial session.
Age in the registry: 18 years to 75 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 |
|---|---|---|---|
| CEU San Pablo University Coordinator of this site? Confirm its status | Madrid | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.