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Relationship of Radiographic Findings With Pain, Function, Physical Performance and Balance

Relationship of Radiographic Findings With Pain, Function, Physical Performance and Balance in Patients With Hip Osteoarthritis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07186374
Enrollment
72
Registered
2025-09-22
Start date
2025-09-20
Completion date
2025-12-31
Last updated
2026-03-17

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

Conditions

Hip Osteoarthritis

Keywords

hip, osteoarthritis, function, balance, radiography

Brief summary

The objective of this investigation was to examine the correlation between radiographic findings and clinical outcomes, including pain, functional ability, physical performance, and balance parameters, in patients diagnosed with hip osteoarthritis (PwHOA).

Detailed description

A total of seventy-two patients with hip osteoarthritis (PwHOA) will be enrolled in the study. Sociodemographic variables will be collected, and assessments will include the Kellgren-Lawrence Classification, Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), Timed Up and Go Test (TUG), and Four Square Step Test (FSST). The Spearman rank correlation coefficient will be employed to analyze the relationships among pain levels, functional capacity, physical performance, balance, and radiographic findings.

Interventions

None listed

Sponsors

Artvin Coruh University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
40 Years to 79 Years

Inclusion criteria

* patients with symptomatic and radiographic diagnosis of Grade I-IV hip osteoarthritis according to the Kellgren-Lawrence classification and American College of Rheumatology criteria.

Exclusion criteria

* patients who did not give consent to participate in the study; * secondary HOA due to rheumatoid arthritis, tumors, and recent fractures; * history of intra-articular injections within the last six months.

Design outcomes

Primary

MeasureTime frameDescription
Kellgren-Lawrence ClassificationSingle assessment at enrollmentThis assessment, acknowledged by the World Health Organization as the definitive standard for the radiographic classification of osteoarthritis, shall be conducted by a qualified orthopaedic specialist. The evaluation will be based on radiographic imaging obtained in both the sagittal and frontal planes while the patient maintains an upright stance. Utilizing the 0-4 severity grading system, a score of '0' denotes the absence of osteoarthritis, whereas a score of '4' signifies advanced, severe osteoarthritic changes.
Western Ontario and McMaster University Osteoarthritis Index (WOMAC)Single assessment at enrollmentThis index, employed for the evaluation of pain, stiffness, and functional impairment, has demonstrated validity and reliability in patients diagnosed with Knee Osteoarthritis (KOA) and Hip Osteoarthritis (HOA), with Intraclass Correlation Coefficients (ICC) ranging from 0.80 to 0.90. It comprises 24 items, each rated on a 5-point Likert scale from 0 to 4, where 0 indicates absence of symptoms, 1 signifies mild symptoms, 2 denotes moderate severity, 3 corresponds to severe symptoms, and 4 reflects extreme severity.
Timed Up and Go Test (TUG)Single assessment at enrollmentThe procedure will initiate with participants seated upright in a chair with their arms resting on their laps. The time required for each participant to rise from a chair elevated to 45 centimeters, traverse a distance of 3 meters at maximum effort, execute a turnaround, and return to the original chair to sit will be measured in seconds utilizing a stopwatch. Following a preliminary trial, the mean duration from two recorded trials will be calculated for analysis.
Four Square Step TestSingle assessment at enrollmentThe assessment of dynamic balance will be conducted utilizing the four-square step test. The test environment will be delineated by arranging bars, each measuring 90 cm in length, in a '+' configuration. The squares will be sequentially numbered clockwise from 1 to 4, commencing with the bottom left square. Participants will be instructed to traverse the squares following the sequence: 2 → 3 → 4 → 1 → 4 → 3 → 2 → 1. The time required to complete the sequence will be measured in seconds using a stopwatch. Following an initial practice trial, the average of two recorded trials will be calculated for analysis.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORZeynep Yıldız Kızkın, Dr.

Artvin Coruh University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026