Burn Outcomes in Young Adult Burn Survivors
- Conditions
- BurnsTrauma
- Interventions
- Other: Questionnaire self report
- Registration Number
- NCT01254357
- Lead Sponsor
- Massachusetts General Hospital
- Brief Summary
As part of Clinical Trials.Gov ID:NCT00253292 a psychometrically sound outcomes instrument was developed to study the outcomes of burn survivors in the 19-30 year old age group. This workgroup has come together to re-examine the data collected during the previous study and determine next steps in understanding the recovery for this population.
- Detailed Description
This study looks to understand previously collected outcomes scores. Identifying young adult burned patients at risk for poor outcomes remains an under-published field of study. We strive to identify problem areas for this population before they adversely effect their quality of life. How are these 19-30 year olds different from their non-burned counterparts and what interventions can we provide to equalize the balance?
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 15
All burn injured young adults with or without skin grafting. All burned young adults on or after their 18th birthday. Between the ages of 19-30 years. English speaking Present for inpatient or outpatient treatment. -
Non-burn skin conditions. Non-English speaking young adults. Young adults less than 19 years of age. Young adults greater than 30 years of age.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description YA Burned Subjects Questionnaire self report Any person between the years of 19-30 years old treated for a burn injury, having incurred within past 12 months.
- Primary Outcome Measures
Name Time Method Short Form Young Adult Outcomes Questionnaire 12-24 month follow-up Once existing data are massaged we will revise the stated outcome measure to make it more contemporary.
- Secondary Outcome Measures
Name Time Method Veterans Rand 12 Item Health Survey (VR-12) 12-24 months follow-up The VR-12 instrument was developed based on data from the SF-36 survey.
Trial Locations
- Locations (6)
Mass General Hospital
🇺🇸Boston, Massachusetts, United States
Shriners Hospital for Children - Boston
🇺🇸Boston, Massachusetts, United States
Shriners Hospital for Children - Galveston
🇺🇸Galveston, Texas, United States
University of Nebraska Medical Center
🇺🇸Omaha, Nebraska, United States
Kennedy Krieger Institute
🇺🇸Baltimore, Maryland, United States
Shriners Hospital for Children
🇺🇸Sacramento, California, United States