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Ultrasound Assessment of Neck Muscles and Balance in Male Patients With Ankylosing Spondylitis

I

Istanbul Physical Medicine Rehabilitation Training and Research Hospital

Status

Enrolling

Conditions

Balance
Spondylarthropathies; Spondylitis, Ankylosing
Balance Assessment
Ankylosing Spondylitis

Treatments

Diagnostic Test: Ultrasonographic assessment of Cervical Multifidus and Longus Colli Muscle Thickness, Postural Balance and Limit of Stability using the balance platform,Cervical Flexion and Extension Strength

Study type

Observational

Funder types

Other

Identifiers

NCT06967883
ISTPMRTRH2024-80

Details and patient eligibility

About

The aim of this study is to evaluate the relationship between ultrasonographic measurements of the cervical muscles and balance parameters in patients diagnosed with ankylosing spondylitis (AS)

Full description

This study aims to investigate the relationship between cervical multifdus and longus Colli muscles and balance function in male patients diagnosed with Ankylosing Spondylitis (AS) according to the Modified New York Criteria. A total of 38 AS patients under regular follow-up at the Istanbul Physical Medicine and Rehabilitation Training and Research Hospital Rheumatology Clinic, along with 38 age-matched healthy male volunteers, will be included.

Ultrasonographic Imaging will be performed to assess the thickness and of the cervical multifidus and longus colli muscles.The HUR SmartBalance BTG4 (HUR-Labs Oy, Kokkola, Finland) balance platform will be used to measure postural sway, weight distribution, and the limit of stability (LOS) through a computerized system.The Berg Balance Scale (BBS), The Timed Up and Go (TUG) test,The Single-Leg Stance Test will be conducted, measuring the ability to maintain posture while standing on one leg. Disease Activity and Functional Assessment in AS Patients will be conducted by using The Bath Ankylosing Spondylitis Functional Index (BASFI), The Bath Ankylosing Spondylitis Metrology Index (BASMI) Additionally, the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) will be used to measure disease activity and quality of life will be assessed with Ankylosing Spondylitis Quality of Life Questionnaire (ASQoL).Cervical Muscle Strength Measurement will be performed using a hand-held dynamometer, which will objectively assess isometric cervical flexion and extension strength.

Enrollment

76 estimated patients

Sex

Male

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18 and 65 years.
  • Diagnosed with Ankylosing Spondylitis according to the Modified New York Criteria (for patient group).
  • Cognitive ability sufficient to understand and follow test instructions.

Exclusion criteria

  • Orthopedic disorders affecting the spine or lower limbs.
  • Cardiovascular disorders.
  • Neurological disorders.
  • Visual or auditory impairments.
  • History of surgery involving the spine or lower limbs.
  • Psychiatric disorders.
  • Cognitive impairment.
  • Clinical signs or symptoms of cervical radiculopathy.

Trial design

76 participants in 2 patient groups

Ankylosing Spondylitis Group
Description:
Male patients aged 18-65 years diagnosed with Ankylosing Spondylitis according to the Modified New York Criteria, under regular follow-up at Istanbul Physical Medicine and Rehabilitation Rheumatology Clinic.
Treatment:
Diagnostic Test: Ultrasonographic assessment of Cervical Multifidus and Longus Colli Muscle Thickness, Postural Balance and Limit of Stability using the balance platform,Cervical Flexion and Extension Strength
Control Group
Description:
Age-matched healthy male volunteers aged 18-65 years with cognitive ability sufficient to understand test instructions.
Treatment:
Diagnostic Test: Ultrasonographic assessment of Cervical Multifidus and Longus Colli Muscle Thickness, Postural Balance and Limit of Stability using the balance platform,Cervical Flexion and Extension Strength

Trial contacts and locations

1

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Central trial contact

Nurdan Paker, MD,Prof.; Ecem Cetin Atakan, MD

Data sourced from clinicaltrials.gov

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