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The Effectiveness of Respiratory Tele-rehabilitation After COVID-19 Pneumonia Related: a Randomized Controlled Trial

Not Applicable
Conditions
Respiratory Rehabilitation
Sars-CoV-2
Dyspnea
ARDS
Coronavirus Infections
Respiratory Failure
Covid19
Interstitial Pneumonia
Quality of Life
Interventions
Other: Telerehabilitation
Registration Number
NCT05007457
Lead Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Brief Summary

In recent months, more and more studies suggest tele-rehabilitation as a means to be exploited to reduce the risk of contagion.

The intent of our study is to verify the effectiveness of a tele-rehabilitation intervention through the application of a respiratory rehabilitation program supported by contact with physiotherapists, in patients with outcomes from SARS-CoV-2 infection discharged from the various medical departments and taken over by physiotherapists after physiatric evaluation.

Faced with the same rehabilitation program prescribed to all patients, the primary objective of our study is to detect whether patients supported by remote rehabilitation after hospitalization improve both adherence to the rehabilitation program and cardiorespiratory endurance and dyspnea symptoms assessed with the Six Minute Walking Test scale (6MWT). This test is validated for multiple pathologies, including idiopathic pulmonary fibrosis, the clinic of which could be comparable to the outcomes of coronavirus interstitial pneumonia as suggested by the literature.

The secondary objectives concern the assessment of the impact of physical exercise assisted by tele-rehabilitation detected through: the assessment of the quality of life (Saint George Respiratory Questionnaire );the assessment of autonomy in daily life activities (Barthel Index Dyspnea Scale), the evaluation of the variation in thoracic expansion and lung volumes (with COACH , an instrument for respiratory physiotherapy that measures the inspiratory volume in ml); the evaluation of muscle strength and endurance (One Minute Sit To Stand) ; the detection of dyspnea during the execution of the exercises (Modified Borg scale); the assessment of the functionality of the lower limbs (Short Physical Performance Battery)

Detailed Description

With regard to respiratory problems, there are still no precise data on the long-term consequences of pulmonary fibrosis and therefore related to the insufficient functioning of the lung. It is possible to hypothesize that these deficiencies can be treated with one specific respiratory rehabilitation aimed at reducing dyspnea and difficulty in practicing daily activities and moving around. In fact, the scientific literature indicates that respiratory rehabilitation improves the quality of life and exercise tolerance of patients with IPF (idiopathic Pulmonary Fibrosis), by reducing respiratory deficits, hypotrophy and muscle weakness, physical deconditioning. Respiratory rehabilitation means a "multidisciplinary intervention based on scientific evidence for patients with chronic respiratory disorders who are symptomatic and often have a reduced quality of life, in need of aerobic and respiratory muscle training, but also oxygen, nutritional, educational, psychological support as well as therapeutic education. For all these reasons we have decided to start our blinded, single-center randomized controlled study, the details of which will be specified later.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Diagnosis of COVID19;
  • Respiratory failure in Sars-Cov2 pneumonia;
  • ARDS in Sars-Cov2 pneumonia;
  • Interstitial pneumonia from Sars-Cov2;
  • Rankin scale ≥ 3/5 before enrollment (therefore at discharge);
  • Patients in need of rehabilitation;
  • Patients discharged from the hospital at their home;
  • Patients with internet access;
  • Owners and users of smartphones / tablets / PCs;
  • Owners a pedal / stationary bike and oximeter.
Exclusion Criteria
  • Asymptomatic or paucisymptomatic patient;
  • Institutionalized person;
  • Unstable angina;
  • Recent IMA;
  • Life expectancy <12 months for other comorbidities (eg advanced cancer).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental GroupTelerehabilitationtelerehabilitation
Control groupTelerehabilitationStandard treatment
Primary Outcome Measures
NameTimeMethod
Six Minute Walking Test (6MWT)through study completion, an average of 1 year

Six Minute Walking Test (6MWT) variation of more than 21.7 meters after 10 weeks of rehabilitation (the least clinically significant variation in patients with IPF - idiopathic pulmonary fibrosis - for the 6MWT is more than 21.7 meters after 6 months of rehabilitation)

Secondary Outcome Measures
NameTimeMethod
Improvement of thoracic expansion and lung volumesthrough study completion, an average of 1 year

COACH (volume incentive used in respiratory rehabilitation)

Improvement of muscle strength and endurancethrough study completion, an average of 1 year

6 minute walking test (6MWT) One Minute Sit To Stand (1MSTS) Short Physical Peformance Battery (SPPB)

Improvement of daily living activitiesthrough study completion, an average of 1 year

Barthel Index Dispnea (BID)

Improvement of the functionality of the lower limbsthrough study completion, an average of 1 year

One Minute Sit To Stand (1MSTS) Short Physical Peformance Battery (SPPB)

Improvement of the quality of lifethrough study completion, an average of 1 year

St. George's Respiratory Questionnaire (SGRQ)

Improvement of dyspnea in the execution of life activitiesthrough study completion, an average of 1 year

Barthel Index Dispnea (BID)

Trial Locations

Locations (1)

Angela Peghetti

🇮🇹

Bologna, BO, Italy

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