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Therapeutic Pulmonary Telerehabilitation Protocol in patients affected by COVID-19, confined in their homes

Therapeutic Pulmonary Telerehabilitation Protocol in patients affected by COVID-19, confined in their homes: Randomized Control Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6m69fc
Enrollment
Unknown
Registered
2020-04-02
Start date
2020-04-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID19

Interventions

Group 1: Respiratory Exercise Program (REP) (n=33) The REP will consist of 10 exercises based on the recommendations made by the official Physiotherapy organizations at the institutional level (Colle
E02.760.169.063.500.387
HP3.073.433.101

Sponsors

Universidad de Sevilla
Lead Sponsor
Universidad de Sevilla
Collaborator

Eligibility

Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients between 18-75 years who are affected by coronavirus (COVID-19), and are in home confinement.

Exclusion criteria

Exclusion criteria: Patients with chronic lung conditions; Patients with chronic kidney disease; Patients affected with chronic neurological disorders; Patients suffering from hypertension and cardiovascular conditions without medical treatment; Patients affected with grade III osteoporosis; Patients affected with acute outbreaks of rheumatologic disorders; Patients affected with acute outbreaks disc abnormalities; Patients who have had respiratory conditions in the last 12 months; Patients who have recent musculoskeletal disorders, and who are not fully recovered from their injuries; Patients who have received physical therapy treatment in the last 3 months; Patients affected with chronic mental and / or psychological disturbances; Red Flags (Night pain, severe muscle spasm, loss of involuntary weight, symptom mismatch)

Design outcomes

Primary

MeasureTime frame
Six Minute Walk Test (6MWT). The 6MWT will be performed by all patients in their home, under the telematically supervision of a physiotherapist. All patients will receive the same instructions before the walk, and will be encouraged by the physiotherapist who repeated set phrases every minute during the walk. The distance covered during the test will be recorded in meters telematically by patient smartphone. Patients will be allowed to stop and rest during the test but they will be instructed to resume walking as soon as they felt able to do so. Patients will send the results of 6MWT screenshot daily to the evaluator, via WhatsApp or email. ;hirty Seconds Sit-To-Stand Test (30STST). Evaluators will ask patients to place a straight-backed armless chair, with a hard seat , which will be stabilized by placing it against a wall, considering floor to seat height will be between 45 - 50 cm. Seated participants will asked to come forward on the seat until their feet will be flat on the floor, and to fold their upper limbs across the chest, without moving it during all test. Patients will be then instructed to stand up all the way and sit down once without using the upper limbs. Patients will start in the seated position on the chair and, upon command telematically, they will stand up, and then they will return to sitting as many times as they could, in a 30-second time period. The evaluators will control this test telematically by videoconference.;Multidimensional Dysphnoea-12 (MD12) Spanish version. The MD12 questionnaire will be self-administered and will be performed at the end of the 6MWT. Patients will send the results of MD12 screenshot daily to the evaluator, via WhatsApp or email.

Secondary

MeasureTime frame
Visual Analog Scale Fatigue (VASF), for fatigue measurement. Patients participating in the study will indicate the intensity of their fatigue by means of the VAS through the Smartphone application called “Visual Scale” (Apple Store and Google Play). They will have to signal in a horizontal line where they would place their fatigue, being 0 "no fatigue" and the 10 would be "the worst imaginable fatigue”. VASF will be controlled telematically by the evaluators through the Smartphone application. The evaluator will ask the patient to indicate their level of VASF in the "Visual Scale" application, and to take a screenshot of the smartphone to obtain the established value for VASF, which is calculated as the average value of two attempts. The patient must send the VASF screenshot daily to the evaluator, via WhatsApp or email.;Borg Scale (BS). The Borg scale, of perceived effort, measures the entire range of effort that the individual perceives when exercising. This scale gives criteria to make adjustments to the intensity of exercise, that is, to the workload, and thus forecast and dictate the different intensities of exercise in sports and medical rehabilitation. The BS will be completed by patients at the beginning of each session, and after completing the exercise program, as well as at the end of the tests, every day (6MWT, 30STST). Patients will send the results of BS screenshot daily to the evaluator, via WhatsApp or email.

Countries

Spain

Contacts

Public ContactCarlos Utrera

Universidad de Sevilla

cbernal495@gmail.com+34627382889

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 26, 2026