Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06252818

Validation of a Digital Platform for Functional Respiratory Rehabilitation

Led by Bio-Sensing Solutions S.L. (DyCare) · Updated on 2024-05-03

100

Participants Needed

1

Research Sites

38 weeks

Total Duration

On this page

Sponsors

B

Bio-Sensing Solutions S.L. (DyCare)

Lead Sponsor

F

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Collaborating Sponsor

AI-Summary

What this Trial Is About

Chronic Obstructive Pulmonary Disease (COPD), characterized by persistent airflow limitation in the respiratory airways, is a chronic condition that affects millions of people worldwide. ReHub enables healthcare professionals to design therapeutic exercise programs for the treatment of COPD patients, as well as to analyze and monitor patient rehabilitation through the information and feedback provided via the platform. The main objective of the study is to evaluate the satisfaction and usability of the ReHub platform (for respiratory rehabilitation) among COPD patients and healthcare professionals. This is a single-center satisfaction and usability study on the usage and experience of the ReHub platform (for respiratory rehabilitation).

CONDITIONS

Official Title

Validation of a Digital Platform for Functional Respiratory Rehabilitation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with COPD, GOLD grade I - IV
  • Need of respiratory rehabilitation
  • 18 years of age or older
  • Explicit willingness to participate in the study
  • Diagnosis of COPD (FEV1/FVC < 70)
Not Eligible

You will not qualify if you...

  • Individuals with cognitive impairment
  • Language barriers or illiteracy (inability to read in Spanish)
  • Lack of access to a mobile device with an internet connection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital de la Santa Creu i Sant Pau

Barcelona, Spain, 08041

Actively Recruiting

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Research Team

C

Carme Puy, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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