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Burn Outcomes in Young Adult Burn Survivors

Completed
Conditions
Burns
Trauma
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
Inclusion Criteria

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. -

Exclusion Criteria

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
GroupInterventionDescription
YA Burned SubjectsQuestionnaire self reportAny person between the years of 19-30 years old treated for a burn injury, having incurred within past 12 months.
Primary Outcome Measures
NameTimeMethod
Short Form Young Adult Outcomes Questionnaire12-24 month follow-up

Once existing data are massaged we will revise the stated outcome measure to make it more contemporary.

Secondary Outcome Measures
NameTimeMethod
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

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