Effects of resistance band training on liver function in burn patients
Response of Liver Enzymes to 12 Weeks of Resistance Band Training Program in Burned Patients.
This study is testing if a 12-week resistance band training program can help improve liver function in burn patients with significant injuries.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 20 Years to 45 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Giza) |
| Trial ID | NCT06067711 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of a 12-week resistance band training program on liver function in patients who have suffered burns covering 30% to 50% of their body surface area. Participants will undergo resistance training three times a week, focusing on various muscle groups, while their serum levels of alanine transaminase (ALT) and aspartate transaminase (AST) will be measured before and after the intervention. The goal is to assess whether this exercise regimen can improve liver function and metabolic health in burned individuals.
Who should consider this trial
Good fit: Ideal candidates are adults aged 20-45 years with burns covering 30% to 50% of their body surface area.
Not a fit: Patients with cardiac diseases, liver diseases, or those who have undergone limb amputations may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could enhance liver function and metabolic health in burn patients, potentially leading to better recovery outcomes.
How similar studies have performed: While resistance training has shown benefits in various populations, this specific application in burn patients is novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: The subject selection will be according to the following criteria: * Age range between 20-45 years. * Male and female patients will participate in the study. * All patients have burn with BBSA about 30% to 50%. * All patients enrolled to the study will have their informed consent. Exclusion Criteria: * The potential participants will be excluded if they meet one of the following criteria: * Cardiac diseases. * Burn of sole of foot. * Exposed hand or foot tendons. * Upper or Lower limb amputation. * History of liver diseases. * Body mass index (BMI=kg/cm2)\<30%.
Where this trial is running
Giza
- Faculty of Physical therapy, Cairo University — Giza, Egypt (Recruiting)
Study contacts
- Study coordinator: A G Elsayed, PHD
- Email: drayasa3ada@yahoo.com
- Phone: 01001475959
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.