Quality of Life Clinical Trial
— COMBEXOfficial title:
"Effects of a Community Based Exercise Program in Adults With Severe Burns"
Verified date | October 2020 |
Source | The University of Texas Medical Branch, Galveston |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this proposal is to assess the efficacy of implementing a 12-week structured and supervised community-based exercise program (COMBEX) at hospital discharge. The investigators will assess the effect of exercise on mental health and physical function, along with its effects on the amelioration of the burn-induced catabolic response. The central hypothesis of this proposal is that exercise-induced physical and psychosocial benefits obtained during a supervised and structured COMBEX program in severely burned adults will improve physical function, and quality of life relative to Standard of Care (SOC).
Status | Completed |
Enrollment | 45 |
Est. completion date | January 1, 2020 |
Est. primary completion date | January 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Patient is >18 = 60 years of age and patient agrees to study; 30% Total Body Surface Area (TBSA) burn or greater; AND has been medically cleared for discharge and exercise participation by the treating burn surgeon. Exclusion Criteria: - The criteria or risk factors that exclude individuals from this study are: - Known history of AIDS, AIDS Related Complex, HIV, - Malignant neuroleptic hyperthermia, - Active tuberculosis, - Arthritis - Cirrhosis, - Cancer within 5 years - Hyperlipidemia - Bone or Endocrine Diseases - Autoimmune Diseases - Chronic Glucocorticoid or non-steroidal anti-inflammatory drug therapy - Renal insufficiency (defined by creatinine >3.0 mg/dl), - Hepatic disease (defined by elevated liver enzymes or bilirubin >3.0 mg/dl), - Known coronary artery disease, - Congestive heart failure, - Uncontrolled asthma or pulmonary disease (e.g. emphysema, COPD), - Associated head injuries requiring specific treatment, - Mental retardation or autism or any other mental disorder, which makes it impossible to participate in an exercise program; - Gastrointestinal disorders which impair absorption. - Pregnancy if applicable |
Country | Name | City | State |
---|---|---|---|
United States | University of Texas Medical Branch | Galveston | Texas |
Lead Sponsor | Collaborator |
---|---|
The University of Texas Medical Branch, Galveston | American Burn Association, United States Department of Defense |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Burn Specific Health Scale Brief (BSHS-B) | The BSHS-B will be used to assess physical functioning and burn injury interference with work activities. The scale for the questionnaire include -0 extremely, 1-Quite a Bit, 2-moderately, 3- a little bit, 4-None (not at All). | Change from discharge from the ICU to 12 weeks post discharge from ICU. | |
Primary | Veterans Rand Health Survey 12-item Health Survey (SF-12) | The SF-12 is a 12-item; self-report questionnaire that yields two subscales: physical health and mental health. | Change from discharge from the ICU to 12 weeks post discharge from ICU. | |
Primary | Return to Work | Self-reported, short questionnaire taking approximately 10 minutes to complete. These questionnaires will assess the present employment status and the time from discharge to return to work, past and current employment status as well as job type and, if applicable, start dates for post-injury positions. Time from discharge to return to work will be measured in weeks. The questionnaire ask yes or questions. Also, two scales from 0-10, rate how difficult is to return to work and how satisfied are they are being back to work. 0 is none, 10 is extremely difficult/extremely satisfied. | 12 weeks post discharge from ICU. | |
Secondary | Peak aerobic capacity | A maximal exercise test on a treadmill using the Modified Bruce protocol. VO2peak will be measured by patient's breathing. | Change from discharge from the ICU to 12 weeks post discharge from ICU. |
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