Burns Clinical Trial
Official title:
Efficacy of Whole-Body Vibration Training on Thermal Burn Injury in Paediatrics: A Prospective Randomized Controlled Trial
Verified date | January 2024 |
Source | Cairo University |
Contact | Hadaya M Eladl |
Phone | +201144814304 |
hd_mos[@]yahoo.com | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
60 Patients with partial and full thickness thermal burns of the lower limb and trunk will be indiscriminately assigned to study group Group A(Study group): 30 patients received whole body vibration training on a vibration platform 12-15 minutes, 5 times per week, plus traditional physical therapy exercise program in the form of 60 minutes supervised exercise program for 8 weeks. Group B (control group):30 patients will receive a traditional physical therapy program. The program consists of 60 minutes of supervised stretching exercise to all involved joints followed by strengthening for affected muscles for 8 weeks.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | August 15, 2024 |
Est. primary completion date | July 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 10 Years to 16 Years |
Eligibility | Inclusion Criteria: 1. Age will range from 10 to 16 years 2. Patients of both sexes. 3. Participants have 25-40 % partial and full thickness burn of the lower limb and trunk. 4. Participants with complete wound healing or after 35-58 days from the start day of the injury. Exclusion Criteria: 1. Patients with open burn wounds in any area of the body. 2. Patients diagnosed with acute rheumatoid arthritis 3. Diabetes, neuropathy, and neurological disorders. 4. Severe behavioral cognitive disorders. 5. Previous brain injury or any disease affecting balance, vestibular or visual disorders. 6. Patients with a history of traumatic spine within the past six months. 7. Patients with a prosthesis, Leg amputation, lower limb deformity, recent fracture or bone disease. |
Country | Name | City | State |
---|---|---|---|
Egypt | Hadaya Mosaad Eladl | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Balance Control: | Biodex balance scale (Biodex medical systems Inc, Shirley, New York, USA), will be used for balance assessment that include overall stability index that is used to assess fluctuations around the zero point representing standard deviations rather than around a group mean. The overall stability index measures the fluctuations from the horizontal along axes of the Biodex stability system. | 2 momths | |
Secondary | Postural Stability | The Berg balance scale includes 14 items with scores from 0 to 4. A score of 0 represents the inability to do the task, while a score of 4 represents the ability to do the task completely, according to the assigned criteria, with 56 indicates the total score. Items range from tasks of simple mobility(e.g. transfers, standing unsupported, sit-to-stand) to tasks with greater difficulty (e.g. tandem standing, turning 360°, single-leg stance). | 2 months. | |
Secondary | Functional Mobility | Timed-up and go test will be used. The test asks the participant to raise up from the sitting position followed by walking for 3 m, turning around, sitting again on the chair with his back supported, and resting his arms on the armrests. | 2 months. | |
Secondary | Muscle Strength | Muscle strength of the quadriceps and hamstring muscles will be assessed using a Biodex System-3 dynamometer (Biodex Medical System, Shirley, NY) prior to and following the 8-weeks intervention. | 2 months. |
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