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

This study has been completed.
ClinicalTrials.gov Identifier:
First Posted: July 26, 2010
Last Update Posted: July 26, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Saint Elizabeth Regional Medical Center

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.


Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Prospective Observational

Resource links provided by NLM:

Further study details as provided by Saint Elizabeth Regional Medical Center:

Study Start Date: May 2009
Study Completion Date: July 2009
Primary Completion Date: July 2009 (Final data collection date for primary outcome measure)

Information from the National Library of Medicine

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Ages Eligible for Study:   19 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Burn Department Nurses and Burn Patients

Inclusion Criteria:

  • nursing staff will be nurses working the evening/night shift beginning at 1900.

Exclusion Criteria:

  • all patients on the ventilator.
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Pam Wiebelhaus, Saint Elizabeth Regional Burn Center
ClinicalTrials.gov Identifier: NCT01169285     History of Changes
Other Study ID Numbers: 609-044
First Submitted: July 22, 2010
First Posted: July 26, 2010
Last Update Posted: July 26, 2010
Last Verified: May 2009

Keywords provided by Saint Elizabeth Regional Medical Center:
Burn Department Nursing Staff