Clinical Trials Directory

Trials / Completed

CompletedNCT01169285

Efficiency and Efficacy of the Distress Thermometer in the Burn and Wound Population (Research Mentoring High Student Project)

Prospective Observational

Status
Completed
Phase
Study type
Observational
Enrollment
Sponsor
Saint Elizabeth Regional Medical Center · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to test the efficiency and efficacy of the Distress Thermometer of patients admitted to the tertiary Burn and Wound Center. The American Cancer Society and the National Comprehensive Cancer Network published treatment guidelines in 2005 adopting the use of the Distress Thermometer as the preferred adjunct assessment tool of a patient's emotional well-being. A literature search provided extension of the tool to a Cardiac Follow-up Clinic. The Distress Thermometer is currently used with oncology patients at Saint Elizabeth. The emotional well being of patients and their significant others is a hallmark of wholistic care. The simple Likert scale of 0-10 has a trigger for further assessment and/ or intervention at four. The validity testing of the tool was done against the Hospital Anxiety and Depression Scale (HADS) and the Brief Symptom Inventory (BSI-18). The purpose of this study is to measure the efficiency and efficacy of the documentation of the Distress Thermometer to patients admitted to a tertiary Burn and Wound Care Center. The frequency of the documentation will be counted and type of documentation will be categorized.

Conditions

Timeline

Start date
2009-05-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2010-07-26
Last updated
2010-07-26

Source: ClinicalTrials.gov record NCT01169285. Inclusion in this directory is not an endorsement.