Idiopathic Pulmonary Fibrosis (IPF) and the 3 Minutes Sit-to-stand Test

NCT ID: NCT03268915

Last Updated: 2019-08-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-09

Study Completion Date

2018-12-09

Brief Summary

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This study is designed to evaluate the reproductibility and the performance of the 3 minutes sit-to-stand test in patients with idiopathic pulmonary fibrosis.

To do this, the investigators are recruiting 40 patients with idiopathic pulmonary fibrosis in 2 centers (Grenoble university hospital and Lyon university hospital).

Patients had to achieve an effort test on a cycle ergometer. 2 visits are planned in the hospital. During each visit, patients will perform a 3 minutes sit-to-stand test, a 1 minute sit-to-stand test and a 6 minutes walk test. During the second visit, patients will also perform a 3 minutes sit-to-stand test with measurement of oxygen uptake.

The investigators will then analyse the results by comparing numbers of cycle, functional response and symptoms during the 3 minutes sit-to-stand test of the 2 visits. The investigators will also compare the functional response obtained during the 3 minutes sit-to-stand test, the 1 minute sit-to-stand test and the 6 minutes walk test.

Finally, the investigators will compare the maximal values of oxygen uptake, respiration rate and expired volume obtained during the 3 minutes sit-to-stand test to the effort test on cycle ergometer.

Detailed Description

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Conditions

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Idiopathic Pulmonary Fibrosis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

The investigators want to test the reproductibility of a 3 minutes sit-to-stand test in patients with idiopathic pulmonary fibrosis.

For this, patient perform the test during 2 visits and the investigators are going to compare the results of the two visits.
Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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patient with idiopathic pulmonary fibrosis

Group Type EXPERIMENTAL

3 minutes sit-to-stand test

Intervention Type DIAGNOSTIC_TEST

3 minutes sit-to-stand test, 1 minute sit-to-stand test, 6 minutes walk test will be performed 2 times for each patients 3 minutes sit-to-stand test with oxygen uptake measurement will be performed one time for each patient

Interventions

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3 minutes sit-to-stand test

3 minutes sit-to-stand test, 1 minute sit-to-stand test, 6 minutes walk test will be performed 2 times for each patients 3 minutes sit-to-stand test with oxygen uptake measurement will be performed one time for each patient

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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6 minutes walk test 1 minute sit-to-stand test 3 minutes sit-to-stand test with oxygen uptake measurement

Eligibility Criteria

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Inclusion Criteria

* man or woman aged less than 85 years
* patients with Idiopathic Pulmonary Fibrosis without any acute exacerbation during 4 months before the inclusion
* Non-opposition to participation in research
* Patient with 6 minutes walk test \> 200 meters (with or without oxygen therapy)

Exclusion Criteria

* Patient with reduced locomotor activity, or joint pain that compromises the performance of the tests
* Patient with 6 minutes walk test \< 200 meters
* Patient with an other etiology of pulmonary fibrosis
* Other significant pulmonary diseases
* Patient with unstable cardiac disease
* Patient who may be, according to the investigator's assessment, not cooperating or respecting the obligations inherent in participating to the study.
* Opposition to participation in research
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU Grenoble Alpes

La Tronche, , France

Site Status

Groupement Hospitalier Est

Lyon, , France

Site Status

Countries

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France

References

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Other Identifiers

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EssaisCliniques_TCL3-FPI

Identifier Type: -

Identifier Source: org_study_id

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