Effectiveness of a Personalized In-home Telerehabilitation Program on Self-Care in Patients with Long COVID

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorCEU San Pablo University

About this trial

The goal of this clinical trial is to evaluate whether a 12-week tele-rehabilitation programme with monitoring via a mobile app produces 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 + 1 scheduled asynchronous session + educational resources * Daily use of the app: daily log, education and questions

Eligibility criteria

Qualifiers

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.

Disqualifiers

Patients with a history of respiratory or cardiovascular diseases prior to COVID-19, other acute or chronic diseases that may interfere with the study

Pregnancy/breastfeeding

Those with contraindications to respiratory muscle training.

Trial design

Treatments tested in this trial

  • Education for self-management
  • Personalised exercise program
  • Usual Care

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators