Digital App for Telerehabilitation in Respiratory Diseases

NCT ID: NCT05572346

Last Updated: 2023-01-10

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 30 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-10-17
• Study Completion Date: 2024-01-31

Brief Summary

The purpose of this study is to evaluate the feasibility and the mid-term effects of a pulmonary rehabilitation intervention, delivered by digital App, on quality of life of patients affected by respiratory diseases. The App will include a monitored exercise training program based on most recent cardiopulmonary rehabilitation guidelines, including alerts, reminders and educational contents as well as chat and online visits with healthcare professionals to improve patient engagement.

Detailed Description

The center-based pulmonary rehabilitation (PR) intervention is considered the gold standard for functional recovery, secondary prevention, quality of life improvement and social as well as work reintegration in patients affected by respiratory diseases. Such kind of intervention, when delivered in all its fundamental components (clinical stabilization, functional assessment, physical and respiratory training, counseling, nutritional intervention and psychosocial support), is able to reduce global mortality and is recommended by the major international guidelines.

Despite the high level of recommendation, only a small fraction of patients after the acute hospital phase is currently initiated to PR programs for several reasons, including the limited number of specialized rehabilitation facilities.

This unmet need can cause a potential damage to patients' health (failure to reduce disability, higher risk of further pathological relapses) and generates an increase in social and healthcare costs, especially related to subsequent hospitalizations and loss of working capacity.

In order to fill the gap between PR need and demand, health systems are have to adopt not only organizational changes but also to implement innovative solutions based on new technologies. In particular, wearables and mobile health devices seem to be promising tools to deliver a sort of "light PR intervention" promoting healthier lifestyle, even in the long term.

Primary aim The primary objective of the study is to evaluate the feasibility and the medium-term effect on quality of life, measured by Visual Analogue Scale (VAS) contained in the EuroQoL 5D-5L questionnaire, of a digital home-based telerehabilitation program in patients with chronic obstructive pulmonary disease (COPD), asthma, bronchiectasis, pulmonary fibrosis, obesity and long COVID syndrome.

Secondary aims The secondary objectives are: to evaluate the impact of the intervention on functional capacity through the Six-Minute Walking test (6MWT); evaluate changes in dyspnea perception; evaluate the impact of the intervention on spirometric indices; evaluate adherence to the intervention delivered via digital app; evaluate usability, satisfaction, adverse events and exacerbations during the intervention delivered through the digital app.

Study design Monocentric, before-after study Assessment a baseline (T0) and after 8 weeks of intervention (T1)

Population 30 patients discharged from the Pulmonary Rehabilitation Unit of ICS Maugeri - IRCCS Lumezzane (Lumezzane - BS, Italy), affected by COPD, asthma, pulmonary fibrosis, bronchiectasis, obesity or long COVID syndrome.

Inclusion criteria Age ≥ 18 years old Diagnosis of COPD with Tiffenau index <70%, FEV1 <80%, asthma, bronchiectasis, pulmonary fibrosis, obesity (BMI > 30), long COVID syndrome Mini-mental status examination >22 Ability to perform a 6MWT with or without assistive devices Patients discharged from the Unit less than two weeks before the enrollment Written informed consent

Exclusion criteria Simultaneous participation to other research projects Simultaneous participation to other rehabilitation interventions High risk of heart failure and/or ventricular dysfunction High thrombotic risk Cardiac surgery within 3 months after the study enrollment High risk of arrhythmias Atrial fibrillation Moderate to severe valvulopathy Severe or not adequately controlled respiratory diseases Hemodynamic instability Anemia (Hb <10 g/dl) Pregnancy History of drugs abuse Total or partial inability to use digital devices Barriers to exercise training completion Full-day ventilotherapy

Materials and methods

At the hospital discharge (T0) a digital kit will be delivered in order to perform a home-based monitored telerehabilitation program. Using this kit, participants will undergo an 8-weeks exercise training and educational program to preserve the rehabilitative outcomes gained during hospital rehabilitation phase.

Every week participants will undergo a video-coaching session with a respiratory physiotherapist.

Primary endpoint Changes EuroQoL 5D-5L VAS score.

Secondary endpoint Change in COPD Assessment Test (CAT) and EuroQoL (VAS excluded) scores Variation of 6MWT performance at 8 weeks (T1) compared to T0 Variations of mean, maximal and at rest saturation during 6MWT at T1 compared to T0 Variations of mean, maximal and at rest heart rate as well as fatigue perception during 6MWT at T1 compared to T0 Change in Barthel Dyspnea and Medical Research Council (MRC) scores Variations of spirometric parameters: FVC, FEV1, Tiffeneau index, FEF75, FEF50, FEF25, FEF25-75 Adherence (number of sessions completed/number of sessions programmed ratio) Satisfaction and user experience assessment with Technology Acceptance Model (TAM) Assessment of adverse events and number of pathological relapses

Sample size Considering a Minimal Clinical Important Difference of 8 points at EuroQoL VAS, a standard deviation of 15 points, an alpha error of 5% and a power of 80%, the estimated sample size will be of 30 participants

Statistical analysis Data will be synthetized using descriptive statistics: quantitative variables will be summarized with means and standard deviations or medians and interquartile ranges, as appropriate; categorical variables will be expressed as absolute frequencies and percentages.

To assess outcomes changes following the 8-weeks intervention, parametric and non-parametric within group tests will be applied as appropriate.

Correlations between variables will be assessed using partial correlation analysis.

All the analyses will be conducted using SPSS 26 (IBM, Armonk, NY, USA).

Ethical and regulatory considerations This study will be conducted in accordance with the principles laid down by the 18th World Medical Assembly (Helsinki, 1964) and all applicable amendments laid down by the World Medical Assemblies, and the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines for Good Clinical Practice.

Conditions

Respiratory Disease; Asthma; Long COVID; Chronic Obstructive Pulmonary Disease; Obesity; Lung Fibrosis; Bronchiectasis

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: PROSPECTIVE

Study Groups

Home-based telerehabilitation group

For each subject, the treatment will lasts 8 weeks. The intervention will include both endurance and resistance exercises as prescribed by the pneumologist at the time of the hospital discharge.

The intervention will be delivered and monitored through a digital app with appropriate sensors.

Home-based telerehabilitation program delivered through digital devices

Intervention Type: OTHER

To evaluate the effects of digital home-based telerehabilitation program on functional and spirometric measures as well as on quality of life in patients with chronic respiratory disease

Interventions

Home-based telerehabilitation program delivered through digital devices

To evaluate the effects of digital home-based telerehabilitation program on functional and spirometric measures as well as on quality of life in patients with chronic respiratory disease

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Diagnosis of COPD with Tiffenau index lower than 70%, FEV1 lower than 80%, asthma, bronchiectasis, pulmonary fibrosis, obesity (BMI higher than 30), long COVID syndrome;
• Mini-mental status examination higher than 22;
• Ability to perform a 6MWT with or without assistive devices;
• Patients discharged from the Pulmonary Rehabilitation Unit less than two weeks before the enrollment;
• Release of written informed consent

Exclusion Criteria

• Simultaneous participation to other research projects;
• Simultaneous participation to other rehabilitation interventions;
• High risk of heart failure and/or ventricular dysfunction;
• High thrombotic risk;
• Cardiac surgery within 3 months after the study enrollment;
• High risk of arrhythmias;
• Atrial fibrillation
• Moderate to severe valvulopathy;
• Severe or not adequately controlled respiratory diseases;
• Hemodynamic instability;
• Anemia (Hb lower than 10 g/dl);
• Pregnancy;
• History of drugs abuse
• Total or partial inability to use digital devices
• Barriers to exercise training completion
• Full-day ventilotherapy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

MedicAir Healthcare S.r.l.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Chiara G Beccaluva, MSc

Role: STUDY_CHAIR

MedicAir Italia S.r.l.

Michele Vitacca, MD

Role: PRINCIPAL_INVESTIGATOR

ICS Maugeri - IRCCS Lumezzane

Locations

ICS Maugeri - IRCCS Lumezzane

Lumezzane, Brescia, Italy

Site Status: RECRUITING

Countries

Italy

Central Contacts

Chiara G Beccaluva, MSc

Role: CONTACT

chiara.beccaluva@medicair.it

0039 342 107 7236

Facility Contacts

Michele Vitacca, MD

Role: primary

michele.vitacca@icsmaugeri.it

Other Identifiers

RE-TEL

Identifier Type: -

Identifier Source: org_study_id