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Telerehabilitation Program in Persistent COVID-19 (COVIDPERS)

U

University of Valencia

Status

Completed

Conditions

Respiratory Disease
Coronavirus Infection

Treatments

Procedure: Walking APP Group
Procedure: Functional APP group

Study type

Interventional

Funder types

Other

Identifiers

NCT04996212
1573778

Details and patient eligibility

About

The syndrome characterized by the persistence of symptoms typical of COVID-19, beyond 4 weeks after discharge, is called long COVID. Long COVID affects a high percentage of patients who have suffered from COVID-19, regardless of its severity. The various symptoms present in that patients affect the functionality and physical, mental and psychological capacities of patients. Therefore, it is necessary to implement therapeutic programs, based on exercises and techniques of physiotherapy, to help affected people to resume their work, family, social and sports activities; prior to illness. Given the context in which these programs must be developed, telecare is positioned as the most recommended care method to carry out the rehabilitation of these patients. The general objective of this study is to evaluate the effectiveness of a cardiorespiratory tele-rehabilitation program in persistent COVID-19 patients. Study participants (n=60) will be randomly assigned to one of two intervention groups. Group 1 will combine breathing exercises with aerobic exercise: walk; and group 2 will perform functional exercises in addition to respiratory physiotherapy with. All participants will be evaluated at the beginning of the intervention, at the end of it.

Enrollment

70 patients

Sex

All

Ages

25 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Who have been diagnosed with coronavirus infection (PCR + and / or Antigen Test +).
  • Have had a mild form of COVID-19 (absence of symptoms or mild symptoms without signs of viral pneumonia or hypoxia).
  • Have overcome such infection; and continue to experience persistent symptoms, including dyspnea, fatigue, and / or functional limitation.

Exclusion criteria

  • Subjects suffering from other pulmonary or cardiac pathologies and / or diabetes, cancer.
  • Individuals who required hospitalization, during the acute stage of infection;
  • People who continue to obtain a positive PCR and / or positive Antigen Test;
  • Those who have not been discharged by their doctor;
  • Subjects who show serious symptoms and / or require medical supervision;
  • Individuals with an inability to handle the internet and devices, such as mobile phones, computers or tablets; essential for telecare

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Triple Blind

70 participants in 2 patient groups

Walking APP Group
Experimental group
Treatment:
Procedure: Walking APP Group
Functional APP Group
Experimental group
Treatment:
Procedure: Functional APP group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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