- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05589922
The Relationship Between Abnormal Modified Schober Index and Demographic Characteristics and Clinical Variables
Determining the Relationship Between Abnormal Modified Schober Index and Demographic Characteristics and Clinical Variables in Patients With Ankylosing Spondylitis
Study Overview
Status
Conditions
Detailed Description
Ankylosing spondylitis (AS), a common type of spondyloarthropathy, is a chronic inflammatory disease that affects spinal joints, and adjacent soft tissues such as sacroiliac joints, tendons, and entheses (1). Inflammation of the spinal structures and progressive changes in the surrounding tissue is largely responsible for decreased physical function and mobility in participants with AS (2).
It is unknown how these parameters of AS participants with AMSI (smaller than 5 cm) are affected compared to AS participants with normal modified Schober index (NMSI, bigger than 5 cm). In addition, it is unclear which demographic characteristics and variables predispose AMSI to occur.
This study will aim to compare AS participants with abnormal modified Schober index (AMSI) versus AS participants with normal modified Schober index (NMSI) in pain, morning stiffness, balance, kinesiophobia and the fear of falling. In addition, the investigators will aim to determine which demographic characteristics and variables predispose AMSI to occur
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Alahan
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Hatay, Alahan, Turkey, 31060
- Hatay Mustafa Kemal University, Faculty of Health Science, Department of Physiotherapy and Rehabilitation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participants who meet the modified New York criteria for AS
- Participants over 18 years
Exclusion Criteria:
- Participants with other concomitant rheumatic diseases (such as fibromyalgia, rheumatoid arthritis, etc.),
- Participants with cognitive or psychiatric disorders,
- Participants with neuromuscular or orthopedic diseases
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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Patients with abnormal modified Schober index
This group will include the patients with Ankylosing Spondylitis who have modified Schober index smaller than 5 cm
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Patients with normal modified Schober index
This group will include the patients with Ankylosing Spondylitis who have modified Schober index bigger than 5 cm
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Modified Schober Index
Time Frame: at baseline
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The measurement of the MSI starts with the subject in an upright posture.
After being determined the posterior superior iliac spines, a horizontal line is drawn at the center of both posterior superior iliac spines.
Ten cm above and five cm below the first line are marked.
The distance between the top and bottom line is remeasured after the patient attempts to flex forward as far as possible while keeping the knees straight
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at baseline
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Bath AS Metrology Index (BASMI)
Time Frame: at baseline
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The BASMI is evulated quantify the mobility of the axial skeleton and includes assessments of lateral lumbar flexion, tragus-to-wall distance, lumbar flexion, intermalleolar distance, and cervical rotation.
Each measure is assigned a score of 0 to 2 with the higher score indicating greater impairment in mobility
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at baseline
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Timed up and go test
Time Frame: at baseline
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It aims to assess mobility and balance.
It measures the time in seconds for a subject to stand up from an armchair, walk 3 m, turn, walk back to the chair, and sit down
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at baseline
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tandem stance test
Time Frame: At baseline
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For the tandem stance test, patients stand holding onto a railing while placing one foot in front of the other.
The researcher standing behind the patient starts timing when the patient's contact with the railing is released.
It is recorded for 30 seconds or until participants contact external support or move out of tandem stance
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At baseline
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Falls Efficacy Scale-International
Time Frame: At baseline
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The FES-I consists of 16 questions questioning how confident patients are in performing activities without falling.
According to the answers, each question is scored between 1 and 4 (1 = not at all concerned, 4 = very concerned), and a higher score is associated with a greater fear of falling
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At baseline
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Tampa Scale for Kinesiophobia
Time Frame: At baseline
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The TSK contains 17 questions which measures fear of movement and/or reinjury.
The scale uses 4-point Likert scoring (1 = entirely disagree, 4 = entirely agree).
A total score ranges from 11 to 44 points and a cut-off point was determined as ≥37 points indicate a high kinesiophobia level
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At baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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functional reach test
Time Frame: At baseline
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For the functional reach test, the patient is asked to stand erect with feet separated from each other in a comfortable position and reach the farthest distance without touching the wall or without taking a step.
The difference in the distance between the starting point and the endpoint is recorded in cm.
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At baseline
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30-second chair sit-to-stand test
Time Frame: At baseline
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The proximal muscle strength and endurance of the lower extremities assessed by the 30-second chair sit-to-stand.
The patients is seated in an armless chair with their back straight, arms crossed in front of the chest, and feet approximately a shoulder width apart and placed on the floor.
Then patients are instructed to fully sit between each stand.
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At baseline
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single leg stance test
Time Frame: At baseline
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For the SLST is performed by standing on one leg (eyes open) barefoot for 20 seconds, the other knee flexed without touching the other leg, with arms are crossed.
The test will be repeated thrice on each foot, and the average time will be used for analysis.
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At baseline
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finger-to-floor distance measure
Time Frame: At baseline
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For finger-to-floor distance (FFD), the subject is asked to perform maximal lumbar flexion while keeping the knees extend.
After which, the distance between the right middle finger and the floor is measured using a tape measure
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At baseline
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Visual Analogue Scale
Time Frame: At baseline
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Pain scores of the patients at night, at rest, and during activity are measured using visual analogue scale (VAS).
(0-10 mm; 0 indicates no pain and 10 indicates severe pain)
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At baseline
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MustafaKU07
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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