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OpenTrials
Completed

NCT Number: NCT01254357

Burn Outcomes in Young Adult Burn Survivors

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.

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Key information

Conditions

Burns Trauma Wounds and Injuries

Age range

19 year–30 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Shriners Hospital for Children, Sacramento, California, United States

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About this study

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?

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

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Treatment and study plan

Questionnaire self report

Other

Burn specific outcome measurement and global health measurement

Other names: Young Adult Burn Outcomes Questionnaire, Veterans Rand 12 Item Health Survey

Primary outcomes

  1. Short Form Young Adult Outcomes Questionnaire

    Time frame: 12-24 month follow-up

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

Secondary outcomes

  1. Veterans Rand 12 Item Health Survey (VR-12)

    Time frame: 12-24 months follow-up

    The VR-12 instrument was developed based on data from the SF-36 survey.

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Shriners Hospitals for Children

Registry information

Official study title

Burn Outcomes in Young Adult Burn Survivors- A Multicenter Outcomes Study

Acronym: YA

Important dates

Study start
2011
Primary completion
2014
Study completion
2015
First posted
Dec 6, 2010
Registry last updated
Oct 6, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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