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NCT05881876
Determining the Reliability and Validity of a New Method for Measuring Upper Extremity Joint Range of Motion in Burn Patients Using a Tracking System
trial in Contracture Joint in 50 participants. Status unknown.
25 December 2023
Quick facts
| Lead sponsor | Hangang Sacred Heart Hospital |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 50 |
| Start date | 15 June 2023 |
| Primary completion | 25 December 2023 |
| Estimated completion | 31 December 2023 |
Conditions studied
- Contracture Joint — all drugs for Contracture Joint →
Sponsor
Hangang Sacred Heart Hospital
Who can join
Adults 18 to 75, any sex, with Contracture Joint. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In burn patients, joint contracture is a common complication caused by hypertrophic scars, necessitating accurate evaluation and diagnosis of the degree of disability and functional deterioration. A standard goniometer based on the American Medical Association (AMA) guidelines for measuring joint range of motion (ROM) is the gold standard for evaluating musculoskeletal diseases. However, the handheld goniometer is highly dependent on the skill and experience of the measurer. Recently, a marker-based system for accurate ROM measurement has been demonstrated in clinical evaluation. This study investigated the reliability and validity of the marker-based system for evaluation of joint ROM in burn patients. Inclusion criteria were as follows: male or female patients between 18 and 75 years of age, partial or full-thickness burns that healed spontaneously or required skin grafting, and limited joint ROM in the upper extremities caused by burns. Exclusion criteria were limited joint ROM due to severe osteoarthritis or rheumatoid arthritis, congenital defects, structural disease, amputation, central or peripheral nervous system injuries, difficulty in voluntary decision-making due to cognitive impairment, or a history of orthopaedic surgery due to fracture. The experimentals tried to compare the validity and reliability of a marker-based system and AMA methods for the burn patient with joint contracture of upper extremities.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Determining the reliability and validity of a new method for measuring upper extremity joint range of motion in patients with burn injury using a tracking system.
Lee SY, Zheng YX, Seo CH, Cho YS, et al · · 2026 · PMID 42012175 · DOI 10.1177/02692155261432011
Verify or expand the search:
- PubMed search for NCT05881876
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
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Related trials
Other Hangang Sacred Heart Hospital trials
Trials by the same sponsor.
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- NCT06563336 — Effects of the EMG-driven Hand Robot Training in Patients With Hand Dysfunction Due to Nerve Damage From Burns · NA · recruiting
- NCT05988905 — The Effects of Gait Performance and Brain Activity After Robot-assisted Gait Training (RAGT) On Patients With Lower Extr · NA · unknown
- NCT06564090 — Effect on Gait Pattern During Robot Assisted Gait Training (RAGT) of End-effector Type in Burn Patients · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05881876 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hangang Sacred Heart Hospital
- Last refreshed: 31 May 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05881876.
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