Viewing Study NCT06447831



Ignite Creation Date: 2024-06-16 @ 11:50 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06447831
Status: RECRUITING
Last Update Posted: 2024-06-07
First Post: 2024-02-02

Brief Title: Assessing Functional Capacity in Directly and Remotely Monitored Home-based Settings A Protocol for a Multinational Validation Study in Individuals With Chronic Respiratory Diseases
Sponsor: Laval University
Organization: Laval University

Study Overview

Official Title: Assessing Functional Capacity in Directly and Remotely Monitored Home-based Settings A Protocol for a Multinational Validation Study in Individuals With Chronic Respiratory Diseases
Status: RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: 6MST
Brief Summary: The goal of this validation study is to provide further evidence of the metrological properties of the 6-minute stepper test in individuals with chronic obstructive pulmonary disease COPD or interstitial lung disease ILD

The main questions it aims to answer are

1 Is the 6-minute stepper test valid when compared to the 6-minute walk test and a maximal cardiopulmonary cycling test
2 Does the 6-minute stepper test give the same results when conducted through direct ie therapist in person and remote ie videoconferencing monitoring
3 Is the 6-minute stepper test safe when conducted at the home of the individual with direct ie therapist in person or remote ie videoconferencing monitoring

Participants will

Conduct the 6-minute stepper test several trials on separate days
Conduct the 6-minute walk test 1 trial on 1 day
Conduct a maximal cardiopulmonary test on a cycle ergometer 1 trial on 1 day
Participate in a semi-structured interview to provide their feedback with regards to the 6-minute stepper test
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None