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NCT07307755Completed

The Validity and Reliability of the Modified O'Sullivan Functional Balance (mOFB) Test for Multiple Sclerosis

Application of the Validity and Reliability of the Modified O'Sullivan Functional Balance (mOFB) Test in Multiple Sclerosis Patients

Source: ClinicalTrials.gov · Last updated 29 Dec 2025

Brief summary (registry, in English)

This study aims to investigate the validity and reliability of the Modified O'Sullivan Functional Balance (OFB) Test, which is used to assess balance in individuals diagnosed with Multiple Sclerosis (MS). Multiple Sclerosis is a chronic nervous system disease that can cause symptoms such as balance problems, difficulty walking, and fatigue, which negatively affect daily life. Balance disorders are common in MS patients, increasing the risk of falls and leading to a decrease in physical activity levels. Therefore, the accurate and reliable assessment of balance in MS patients is of great importance. This study will include volunteer MS patients treated at the Physical Therapy and Rehabilitation Department of SANKO University Sani Konukoğlu Application and Research Hospital who meet the inclusion criteria. After recording the participants' demographic and disease-related information, their balance, body control, and walking skills will be assessed using various clinical tests. These tests include the Berg Balance Test, Mini-BESTest, O'Sullivan Functional Balance Test, Modified O'Sullivan Functional Balance Test, Trunk Instability Scale, and L Test. Assessments will be conducted taking into account the fatigue commonly seen in MS patients, and participants will be allowed to rest when needed. The results obtained will reveal whether the Modified O'Sullivan Functional Balance Test is a reliable and applicable method for assessing balance in MS patients. It is anticipated that the results of this study will contribute to clinical practice in the assessment of balance in MS patients and assist in the more effective planning of the rehabilitation process.

Status (registry)
Completed
Study type
Observational
Enrollment
44 (actual)
First submitted
15 Dec 2025
Start date
1 Aug 2025
Primary completion date
1 Sept 2025
Lead sponsor
Sanko University
NCT number
NCT07307755

What you commit to

  • Study type: Observational
  • Participants enrolled: 44
  • From 1 Aug 2025 to the primary completion date, 1 Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Received corticosteroid treatment within the last month
  • Took any medication affecting walking ability within the last month

Other

  • Pregnant or within the first 3 months postpartum

Who the study is looking for

  • Participants aged 18-65 years
  • Volunteers participating in the study
  • Individuals not using any assistive devices
  • Individuals unable to maintain the tandem stance test for more than 10 seconds
  • Individuals with an Expanded Disability Status Scale (EDSS) score ≤ 5.5

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sanko Unıversıty
Coordinator of this site? Confirm its status
GaziantepTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.