Evaluating upper limb recovery after burn injuries with physiotherapy
Changes in Function of the Upper Limb With Physiotherapy for Acute Burns: a Pilot Study
This study is testing how physiotherapy can help patients with severe burn injuries on their arms recover better by improving their movement, strength, and overall function.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 17 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Lithuanian University of Health Sciences Academic / other |
| Locations | 1 site (Kaunas) |
| Trial ID | NCT06139731 on ClinicalTrials.gov |
What this trial studies
This pilot clinical study aims to assess the changes in range of motion (ROM), muscle strength, and functional recovery of the upper limb in patients undergoing inpatient treatment for burn injuries. It includes 17 patients with varying degrees of burns on the upper limbs, focusing on those with significant burns covering 10% or more of the total body surface area. The study seeks to understand how physiotherapy can aid in reducing complications such as contractures and scarring during the recovery process.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-69 with burns on the upper limbs that cover at least 10% of their total body surface area.
Not a fit: Patients with other significant injuries or conditions affecting their ability to participate in rehabilitation may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance rehabilitation strategies for burn patients, leading to improved recovery outcomes and quality of life.
How similar studies have performed: While this approach is not widely tested, similar studies have shown promising results in improving recovery outcomes for burn patients through targeted physiotherapy.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients aged 18-69 years * had burns on the upper limb(s) with or without burns on the upper body * burns involving ≥ 10% total body surface area (TBSA) with the presence of deep partial thickness or full thickness burns * who agreed to take part in the study Exclusion Criteria: * inability to perform or understand tests * other injuries (fractures, brain injury) * central and peripheral nervous system disorders * amputation * with burns on the head, hands, feet, and genital area
Where this trial is running
Kaunas
- Brigita Siparytė-Sinkevičienė — Kaunas, Lithuania (Recruiting)
Study contacts
- Principal investigator: Rytis Rimdeika, Prof — Lithuania LUHS hospital Kaunas Clinics, Department of Plastic and Reconstructive Surgery
- Study coordinator: Brigita Siparytė-Sinkevičienė
- Email: brigita.siparyte@lsmu.lt
- Phone: +37068294149
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.