Actively Recruiting
Incidence and Determinants of Joint Contractures in Mechanically Ventilated ICU Patients
Led by Elazıg Fethi Sekin Sehir Hastanesi · Updated on 2026-01-14
150
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective observational cohort study aims to evaluate the incidence and determinants of joint contracture development in mechanically ventilated adult patients admitted to the intensive care unit (ICU). Prolonged immobilization, deep sedation, and neuromuscular blockade are common in critically ill patients and may contribute to musculoskeletal complications, including joint contractures, which can adversely affect functional outcomes and rehabilitation after ICU discharge. Adult patients who are mechanically ventilated, immobilized, and have impaired consciousness will be consecutively enrolled and followed during their ICU stay. Joint range of motion will be assessed using standardized passive range of motion (PROM) measurements performed with a goniometer at predefined intervals by trained assessors. Joint contracture will be defined as a reduction of at least 33% in passive joint range of motion compared with normal reference values. This study is non-interventional, and all patients will receive routine ICU care and standard physiotherapy according to institutional protocols. No additional procedures or interventions will be applied for research purposes. Demographic characteristics, clinical variables, and ICU-related factors will be recorded to explore potential associations with contracture development. The findings of this study are expected to provide prospective data on the burden of joint contractures in mechanically ventilated ICU patients and to identify modifiable risk factors that may inform future preventive and rehabilitative strategies in critical care practice.
CONDITIONS
Official Title
Incidence and Determinants of Joint Contractures in Mechanically Ventilated ICU Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18 and over
- Patients on mechanical ventilation and monitored in the intensive care unit for at least 7 days
- Glasgow Coma Score 10 or lower
- Patients monitored immobile in the intensive care unit
- Situations where informed consent can be obtained from the patient's legal representative
You will not qualify if you...
- Presence of pre-existing joint contracture, ankylosis, or amputation
- Patients with severe burns, fractures, or surgical reasons preventing joint movement
- Patients with a history of neuromuscular disease or spasticity
- Patients who were immobilized for 1 week or more prior to admission to the intensive care unit
- Hemodynamic instability situations where measurement is unreliable
AI-Screening
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Trial Site Locations
Total: 1 location
1
Fethi Sekin City Hospital
Elâzığ, Elaziğ, Turkey (Türkiye), 23050
Actively Recruiting
Research Team
S
Sevim F Şenol Karataş, MD, PhD
CONTACT
S
Sevim Şenol Karataş, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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