- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06859567
Chester Step Test: is It Effective in Scleroderma Patients?
February 28, 2025 updated by: Havvagül Doğan, Firat University
Proving the Efficacy of the Chester Step Test in Scleroderma Patients Compared with the 6-Minute Walk Test
Systemic sclerosis (SSC) is a chronic autoimmune disease in which autoimmune features are associated with vascular manifestations.
Patients with SSC experience many problems such as interstitial lung disease (ILD), pulmonary arterial hypertension (PAH), heart failure, severe gastrointestinal tract (GIT) involvement and scleroderma renal crisis (SRC).
Because of these problems, SSC patients may develop an abnormal pulmonary hemodynamic response during exercise.
In this situation, measuring the aerobic capacity of SSC patients can be a useful tool for health promotion.
There are many different methods for measuring aerobic capacity tests.
The most commonly used aerobic capacity test in SSC patients is the 6-minute walk test (6 MWT).
However, although the 6 MWT is a commonly used test, it has some disadvantages.
Because SSC affects multiple organs, there are doubts about the 6 MWT's ability to accurately assess these diseases.
These disadvantages of the 6MWT have led to the search for new tests.
The Chester step test (CST) is a submaximal test and a good option to assess aerobic capacity.
An adapted version of the CST for non-healthy individuals can be used to assess aerobic capacity.
There are some studies conducted with CST.
As a result of my research, no study evaluating CST in individuals with SSC was found.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Detailed Description
Systemic sclerosis (SSC) is a chronic autoimmune disease with autoimmune features combined with vascular manifestations.
Systemic sclerosis (SSC), the main symptom of which is skin sclerosis, is a marker that can detect the activity of the disease.
Apart from skin involvement, SSC affects many internal organs such as the musculoskeletal system, gastrointestinal system, lungs, heart and kidneys.
Because of these problems, SSC patients may develop an abnormal pulmonary hemodynamic response during exercise.
This can lead to symptoms of dyspnea, fatigue and decreased exercise tolerance.
In this situation, measuring the aerobic capacity of SSC patients can be a useful tool in health promotion.
There are many different methods for measuring aerobic capacity tests.
The most commonly used aerobic capacity test in SSC patients is the 6-minute walk test (6 MWT).
However, although the 6 MWT is a commonly used test, it has some disadvantages.
Because SSC affects multiple organs, there are doubts about the 6 MWT's ability to accurately assess these diseases.
For an accurate 6MWT assessment, a 30 meter corridor is needed.
This length of corridor is impossible to access in some clinics.
These disadvantages of the 6MWT have led to the search for new tests.
The Chester step test (CST) is a submaximal test and a good option for assessing aerobic capacity.
Compared to 6 MWT, CST has the advantage of requiring portable equipment.
It is a cost-effective option to assess exercise tolerance, fatigue and dyspnea.
Because of these advantages of the CST, it can be used to assess aerobic capacity when adapted to non-healthy individuals.
There are some studies conducted with CST.
As a result of my research, no study evaluating CST in individuals with SSC was found.
The study will be conducted at Firat University Hospital and 45 patients will be evaluated.
After the demographic data of the patients included in the study are recorded, 6MWT will be performed and the results will be recorded.
Then CST will be performed and the results will be recorded.6
Dyspnea, fatigue and leg fatigue will be evaluated with the Modified Borg Scale before and after MWT and CST.
The patient's heart rate, oxygen saturation and blood pressure will be recorded before and after the tests.
In addition, the patient's heart rate and oxygen saturation will be recorded after each level passed in CST.
Study Type
Interventional
Enrollment (Estimated)
45
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Havvagül Doğan
- Phone Number: +90 4242370000
- Email: havvvaguldogan@gmail.com
Study Locations
-
-
Elazığ
-
Merkez, Elazığ, Turkey, 23000
- Firat University
-
Contact:
- Havvagül Doğan
- Phone Number: +90 424 2370000
- Email: havvvaguldogan@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Over 18 years old
- Patients who can walk independently without an assistive device
Exclusion Criteria:
- Chronic obstructive pulmonary disease
- Myocardial infarction history
- Congestive heart failure
- Serious or unstable illness that may limit exercise tolerance
- Presence of severe musculoskeletal and joint disorders that may interfere with the conduct of the test
- Inability to perform the simplest level of the Chester step test
- Arthroplasty or major operations on knee and hip joints
- Uncontrolled hypertension
- Lack of ability to understand and implement all recommended procedures
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Evaluated Group
6 minute walk test, Chester step test
|
Comparison of the 6-minute walk test and Chester step test, one of the aerobic capacity tests
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Modified Borg Scale
Time Frame: up to 30 minutes
|
The modified Borg scale is a validated scale for subjective perception of dyspnea used with the 6MWT to confirm the degree of respiratory distress.
Exercise intensity is determined by individualized measurement.
The 2002 guidelines of the American Thoracic Society recommend the modified Borg scale as an adjunct to the 6MWT.
This scale is a vertical scale measured from 0 to 10.
Here 0 represents no symptoms and 10 represents maximum symptoms.
In this study, the modified Borg scale will be used to rate dyspnea and leg fatigue.
The Borg scale will be printed out and this printout will be used for patient enumeration.
The patient will be told what the numbers from 0 to 10 on the Borg scale mean.
After instructions have been given, the patient will be asked to rate dyspnea and leg fatigue before and after the test and the numbers will be recorded.
|
up to 30 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 11, 2025
Primary Completion (Estimated)
June 15, 2025
Study Completion (Estimated)
July 15, 2025
Study Registration Dates
First Submitted
February 28, 2025
First Submitted That Met QC Criteria
February 28, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 28, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/03-16
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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