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Comparison of the 1-min Sit-to-Stand Test to the 6-minute Walk Test in the Respiratory Functional Assessment of Pulmonary Fibrosis (LaMinute_FIP)

Primary Purpose

Idiopathic Pulmonary Fibrosis

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
TLC1_TM6
TM6_TLC1
Sponsored by
Fondation Hôpital Saint-Joseph
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Idiopathic Pulmonary Fibrosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient whose age is ≥ 18 years
  • Patient with fibrosing interstitial lung disease
  • French-speaking patient
  • Patient affiliated to a health insurance plan
  • Patient who has given free, informed and written consent

Exclusion Criteria:

  • Patient with an exacerbation of fibrosis in the last 6 months
  • Patient with comorbidities limiting exercise performance
  • Distance traveled < 200m at TM6
  • Patient on long-term oxygen therapy (LTO)
  • Patient already included in a type 1 interventional research protocol (RIPH1)
  • Patient under guardianship or curatorship
  • Patient deprived of liberty
  • Patient under court protection
  • Pregnant or breastfeeding patient

Sites / Locations

  • Groupe Hospitalier Paris Saint-JosephRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

TLC1_TM6

TM6_TLC1

Arm Description

Patient doing 1-minute chair lift test (TLC1) before 6-minute Walk Test (TM6).

Patient performing 6-minute Walk Test (TM6) before 1-minute chair lift test (TLC1)

Outcomes

Primary Outcome Measures

Strength of the relationship between O2 desaturation obtained with WT-6 and TLC1 at Day 1
This outcome corresponds to the difference of O2 desaturation obtained with TM6 and TLC1.

Secondary Outcome Measures

Equivalence of the percentage of desaturation on the TM6 and the TLC1
This outcome corresponds to the Difference between initial SaO2 and final SaO2. The objective is to test the equivalence of the percentage of desaturation between these 2 parameters obtained with the TM6 and the TLC1.
Strength of the relationship between O2 desaturation obtained with WT-6 and TLC1 at month 6
This outcome corresponds to nadir of O2 desaturation obtained with TM6 and TLC1.

Full Information

First Posted
June 29, 2022
Last Updated
September 30, 2022
Sponsor
Fondation Hôpital Saint-Joseph
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1. Study Identification

Unique Protocol Identification Number
NCT05449431
Brief Title
Comparison of the 1-min Sit-to-Stand Test to the 6-minute Walk Test in the Respiratory Functional Assessment of Pulmonary Fibrosis
Acronym
LaMinute_FIP
Official Title
Comparison of the 1-min Sit-to-Stand Test to the 6-minute Walk Test in the Respiratory Functional Assessment of Pulmonary Fibrosis: a Cross-over Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 8, 2022 (Actual)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
December 5, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondation Hôpital Saint-Joseph

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Fibrosing interstitial lung diseases or pulmonary fibrosis represent a heterogeneous group of progressive pulmonary pathologies, responsible for a significant morbi-mortality. They are defined by an infiltration of the pulmonary interstitium associating in a variable way an inflammatory component (deposit of inflammatory cells) and a fibrosing component (deposit of collagen). Idiopathic pulmonary fibrosis (IPF) is the most common and most severe pulmonary fibrosis. Other pulmonary fibroses are mainly represented by non-specific interstitial lung disease, pulmonary fibroses associated with connectivites, hypersensitivity pneumonitis, certain pneumoconiosis (occupational diseases) and sarcoidosis. The process of fibrosis is responsible for a loss of elasticity of the lung, leading to a decrease in lung volumes associated with an alteration of gas exchange. In these diseases, the clinician must be able to rely on reliable means to assess the severity of the disease based mainly on the measurement of lung volumes and gas exchange, at diagnosis and in the follow-up of the patient, in order to propose the most appropriate management. Lung volumes are assessed by respiratory function tests. Forced vital capacity is the reference volume value used. Impaired gas exchange is assessed at rest by measuring carbon monoxide diffusion capacity, arterial oxygen saturation and arterial blood gases. The functional capacity to exercise is also a very important evaluation criterion in terms of prognosis and in the follow-up of the patient. It is assessed by means of ergocycle tests which mainly determine the maximal oxygen consumption. These are relatively complex tests that require special equipment and are not routinely performed. Simpler field tests have been developed to assess functional capacity during exercise, the most widely used and validated being the 6-minute Walk Test (TM6). Other field tests to assess functional capacity to exercise have been developed, such as the 30-second, 1-minute, and 3-minute chair lift tests, stepper tests, and step and stair tests. Among them, the 1-minute chair lift test (TLC1) is the best evaluated. It consists of sitting down and getting up from a chair as many times as possible in 1 minute. The criteria measured are mainly the number of lifts and desaturation. Thus, the fundamental advantage of the TLC1 over the TM6 is the exemption from temporal and spatial constraints since it takes only a few minutes and can be performed in a medical office. While TLC1 seems to be the most suitable, there are still a few pitfalls in substituting TLC1 for TM6 during diffuse interstitial lung disease. First, there is only one study reporting the results of TLC1 in a healthy population. It provides a chart of results according to age. Unfortunately, only the number of lifts is reported without any data on heart rate, SaO2 or sensation of dyspnea. In respiratory pathologies, TLC1 has been studied mainly in patients with chronic obstructive pulmonary disease (COPD) and little in PID. Unlike TM6, TLC1 is reproducible and has no learning effect in this population. Interestingly, one study found that peak desaturation and peak oxygen consumption occurred during the recovery phase some seconds after the end of the test. Studies on TLC1 during SID do not allow us to conclude that this test can substitute for TM6. However, investigators may note certain limitations, in particular the small number of patients studied and the retrospective nature of the 2 largest of them. Above all, it seems that the use of TLC1 could be optimized by taking into account the recovery phase in the evaluation of desaturation. The hypothesis of our study is that the TLC1 taking into account the recovery phase can replace the TM6 in the management of fibrosing PID for prognostic evaluation, patient follow-up and indication of oxygen therapy. It is more accessible and its use by all practitioners in face-to-face or telemedicine would allow a better management of these patients. Finally, the investigators hypothesize that the TLC1 will result in lower costs in the management of these patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Pulmonary Fibrosis

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TLC1_TM6
Arm Type
Experimental
Arm Description
Patient doing 1-minute chair lift test (TLC1) before 6-minute Walk Test (TM6).
Arm Title
TM6_TLC1
Arm Type
Experimental
Arm Description
Patient performing 6-minute Walk Test (TM6) before 1-minute chair lift test (TLC1)
Intervention Type
Other
Intervention Name(s)
TLC1_TM6
Intervention Description
Following this inclusion, patients are performing 1-minute chair lift test (TLC1) before 6-minute Walk Test (TM6). Each exercise will be separated by 30 minutes during which the patient will be sitting in a waiting room.
Intervention Type
Other
Intervention Name(s)
TM6_TLC1
Intervention Description
Following this inclusion, patients are performing 6-minute Walk Test (TM6) before 1-minute chair lift test (TLC1). Each exercise will be separated by 30 minutes during which the patient will be sitting in a waiting room.
Primary Outcome Measure Information:
Title
Strength of the relationship between O2 desaturation obtained with WT-6 and TLC1 at Day 1
Description
This outcome corresponds to the difference of O2 desaturation obtained with TM6 and TLC1.
Time Frame
Day 1
Secondary Outcome Measure Information:
Title
Equivalence of the percentage of desaturation on the TM6 and the TLC1
Description
This outcome corresponds to the Difference between initial SaO2 and final SaO2. The objective is to test the equivalence of the percentage of desaturation between these 2 parameters obtained with the TM6 and the TLC1.
Time Frame
Month 6
Title
Strength of the relationship between O2 desaturation obtained with WT-6 and TLC1 at month 6
Description
This outcome corresponds to nadir of O2 desaturation obtained with TM6 and TLC1.
Time Frame
Month 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient whose age is ≥ 18 years Patient with fibrosing interstitial lung disease French-speaking patient Patient affiliated to a health insurance plan Patient who has given free, informed and written consent Exclusion Criteria: Patient with an exacerbation of fibrosis in the last 6 months Patient with comorbidities limiting exercise performance Distance traveled < 200m at TM6 Patient on long-term oxygen therapy (LTO) Patient already included in a type 1 interventional research protocol (RIPH1) Patient under guardianship or curatorship Patient deprived of liberty Patient under court protection Pregnant or breastfeeding patient
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean Marc NACCACHE, MD
Phone
144127582
Ext
+33
Email
jmnaccache@ghpsj.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Helene BEAUSSIER, PharmD, PhD
Phone
144127883
Ext
+33
Email
crc@ghpsj.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Marc NACCACHE, MD
Organizational Affiliation
Fondation Hôpital Saint-Joseph
Official's Role
Principal Investigator
Facility Information:
Facility Name
Groupe Hospitalier Paris Saint-Joseph
City
Paris
ZIP/Postal Code
75014
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Helene BEAUSSIER, PharmD, PhD

12. IPD Sharing Statement

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Comparison of the 1-min Sit-to-Stand Test to the 6-minute Walk Test in the Respiratory Functional Assessment of Pulmonary Fibrosis

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