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3 Minutes Chair Rise Test (3CRT) in Patients With COPD

Chair Rise Tests for a Simplified Evaluation of Functional Response After a Rehabilitation Program in Patients COPD.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03286660
Acronym
3CRT
Enrollment
127
Registered
2017-09-18
Start date
2014-12-08
Completion date
2017-07-24
Last updated
2017-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD, Evaluations, Rehabilitation

Keywords

Exercise tests, COPD, Rehabilitation

Brief summary

Improvement in the functional functioning and dyspnea of COPD patients after a rehabilitation program (RHB) is assessed by exercise tests and questionnaires difficult to replicate outside specialized centers. In order to monitor the eventual decline of patients in the course of their RHB management, Chair Rise Tests (3CRT-1CRT-5STS) and short questionnaires were developed (CAT-DIRECT). The goal of this prospective, multicenter, real-life study is to compare the change in several functional function tests and questionnaires of quality of life and dyspnea related to daily activities. In addition, MCIDs of the 3CRT and the DIRECT questionnaire (Disability Related to COPS Tool) were specified.

Interventions

DIAGNOSTIC_TESTChair Rise Tests and short questionnaire

Exercises consist on a Chair Rise Tests and short questionnaire It is a functional test evaluating the number of chair rise over a given time and / or frequency. This test is combined with a questionnaire to collect quantitative and qualitative information: * dyspnea and muscular fatigue at rest before the start of the test and at the end of the exercise * Saturation at rest, and at the end of the exercise * the number of total a chair rise

Sponsors

Boehringer Ingelheim
CollaboratorINDUSTRY
HYLAB, Physiopathologie de l'exercice
CollaboratorUNKNOWN
University Hospital, Lille
Lead SponsorOTHER

Study design

Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patient with COPD Gold II to IV * Patient admitted for a rehabilitation program in real life * Person affiliated to the Social Security or beneficiary of such a scheme * Informed and written consent by patient or legal representative

Exclusion criteria

* Patient limited by reduced locomotor activity or joint pain that compromises their participation in a rehabilitation program * Patients with a performance less than 250 meters during 6MWT * Non-stable cardiac disease * Any other lung disease than COPD * Person subject to a legal protection measure

Design outcomes

Primary

MeasureTime frameDescription
Change of number of rise during 3 minutes Chair Rise Test (3CRT)At Baseline, at 2 and 8 weeks.The change of total number of rise during a 3 minutes Chair Rise Test (3CRT) from baseline

Secondary

MeasureTime frameDescription
Change of Time to perform 5 sit to standAt Baseline, at 2 and 8 weeks.The change of Time to perform 5 sit to stand from baseline
The change of Total score for the DIsability RElated to COPD Tool (DIRECT)At Baseline and at 8 weeks.Total Score
Change of number of rise during 1 minute Chair Rise Test (1CRT)At Baseline, at 2 and 8 weeks.The change of total number of rise during a 1 minutes Chair Rise Test (3CRT) from baseline
Change in endurance time at constant power on cyclo ergometer,At Baseline, at 2 and 8 weeks.The change of endurance time from baseline
Change of Voluntary Quadriceps force outputAt Baseline, at 2 and 8 weeks.Change of Voluntary quadriceps force measurements (Mean of 3 maximal measurements) from baseline
Difference in physiological response (SpO2 and HR) during the 3 Chair Rise Tests (3CRT-1CRT-5STS)At Baseline, at 2 and 8 weeks.End SpO2 - End Heart Rate

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026