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Clinical Trials/NCT06263699
NCT06263699
Completed
Not Applicable

Comparing the Accuracy of Clinical Goniometry and Goniometric Measurement on Standardised Images in Dupuytren's Disease

Universitaire Ziekenhuizen KU Leuven1 site in 1 country59 target enrollmentJanuary 29, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dupuytren's Disease
Sponsor
Universitaire Ziekenhuizen KU Leuven
Enrollment
59
Locations
1
Primary Endpoint
Active Extension Deficits (AED)
Status
Completed
Last Updated
9 months ago

Overview

Brief Summary

Measuring range of motion (ROM) is essential in detecting musculoskeletal deficits, monitoring the effects of treatment and progression of the disease. In Dupuytren's disease the active and passive extension deficits (AED, PED) of digits 4 and 5 are usually clinically measured using a universal, short arm goniometer which is considered the standard of care. Using the goniometer can be time consuming. Measuring the extension deficit on a standardised picture could improve follow up, since it is a faster and easier process to take a picture and upload it to the patients files. Though this gives rise to the question whether this kind of measurement would be equally accurate and reliable in comparison to regular clinical measurement using a goniometer.

Detailed Description

Measuring range of motion (ROM) is essential in detecting musculoskeletal deficits, monitoring the effects of treatment and progression of the disease. In Dupuytren's disease the active and passive extension deficits (AED, PED) of digits 4 and 5 are usually clinically measured using a universal, short arm goniometer which is considered the standard of care. Using the goniometer to measure the extension deficit of both fingers, for both the proximal interphalangeal (PIP) and metacarpophalangeal (MCP) joint can be a time consuming process. A lot of clinicians have limited time per patient, which leads to partially or completely missing data due to not performing the measurements. Measuring the extension deficit on a standardised picture could improve follow up, since it is a faster and easier process to take a picture and upload it to the patients files. Though this gives rise to the question whether this kind of measurement would be equally accurate and reliable in comparison to regular clinical measurement using a goniometer. Establishing the difference between both methods is essential to monitor change, which makes a statistical comparison of accuracy of both methods very valuable for patients with Dupuytren's disease. Furthermore, a lot of clinicians have collected and stored standardised pictures of their patient's hands over the years. Therefore this study could solidify the available data through these images, which provide valuable information for future follow up. Furthermore, proper patient education could provide the clinician with standardised images taken by the patient himself, leading to improved follow up, if images and clinical measurement prove to be equally accurate.

Registry
clinicaltrials.gov
Start Date
January 29, 2024
End Date
March 3, 2025
Last Updated
9 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Older than 18 years of age
  • Current AED in digit 4 or 5, in the MCP or PIP joint

Exclusion Criteria

  • Abnormalities to the fingers other than Dupuytren's disease which make goniometry impossible (e.g. amputation, arthrodesis of finger joints, deformations due to rheumatoid arthritis etc.)
  • Patient's unable to give a written participating consent.
  • Younger than 18 years of age.

Outcomes

Primary Outcomes

Active Extension Deficits (AED)

Time Frame: Baseline

AED in the MCP and PIP joints of digit 4 and 5 are measured by using a goniometer

Study Sites (1)

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