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NCT01161810 Clinical Trial

The Relationship of Rehabilitation Therapy Time To The Prevention of Burn Scar Contracture

Burns Clinical Trial

— ACT  

Official title:
Burn Patient Acuity Demographics, Scar Contractures and Rehabilitation Treatment Time Related to Patient Outcomes (ACT)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01161810
Other study ID # ABA-MCTG-0003
Secondary ID H-08-028
Status Completed
Phase
First received
Last updated
Start date July 2010
Est. completion date September 2014

Study information
Verified date August 2023
Source American Burn Association
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This project will develop a descriptive database of patient information and patient outcomes. This database will be used to determine the association of time spent in rehabilitation and patient outcomes, to relate patient acuity to burn scar contracture development and to establish minimal time requirement guidelines for various rehabilitation patient outcomes.

Recruitment information / eligibility
Status Completed
Enrollment 386
Est. completion date September 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - 18 year of age or older - Admission for primary diagnosis of cutaneous burn injury - Anticipated length of stay equal to/greater than five days - >2% deep partial thickness burn OR hand burn (which may be less than 2% deep partial thickness burn) Exclusion Criteria: - Non-survivable burn as determined by the attending burn surgeon - Electrical burn injury

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Routine post burn rehabilitation therapy
No testing outside of routine clinical rehabilitation will be performed

Locations
Country Name City State
United States The University of North Carolina at Chapel Hill Chapel Hill North Carolina
United States U.S. army Institute of Surgical Research Fort Sam Houston Texas
United States St. Joseph Regional Burn Center Fort Wayne Indiana
United States University of Iowa Hospitals and Clinics Iowa City Iowa
United States St Elizabeth Regional Medical Center Lincoln Nebraska
United States Loyola University Health System Maywood Illinois
United States NewYork-Presbyterian Weill Cornell Medical Center New York New York
United States University of Califronia Irvine Orange California
United States Arizona Burn Center Phoenix Arizona
United States Oregon Burn Center, Legacy Emanuel Hospital & Health Center Portland Oregon
United States University of California Davis, Regional Burn Center Sacramento California
United States Regions Hospital Burn Center Saint Paul Minnesota
United States University of Utah Health Services Center Salt Lake City Utah
United States Via Christi Regional Burn Center Wichita Kansas

Sponsors (2)
Lead Sponsor Collaborator
American Burn Association U.S. Army Medical Research and Development Command

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measure patient outcome in terms of time devoted to rehabilitation Standard information that is recorded as part of daily routine in the rehabilitation treatment of patients with burn injury will be used as data to analyze patient outcomes At discharge
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