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Increasing Patient Preparedness for the Procedural Experience and Improving Qualitative Outcomes Through Patient Education
Objective: To compare changes in patient anxiety levels between groups of patients who either were or were not exposed to an informative multimedia patient education tool, in order to determine how the addition of such a multimedia tool will affect this parameter. Specifically, the study will focus on subjective anxiety as measured on pre procedure and post procedure patient surveys as detailed under study components.
If you agree to take part in this study, you will complete a questionnaire that asks how you feel before the procedure. It will take about 5 minutes to complete. After you have completed the questionnaire, you will be randomly assigned (as in the flip of a coin) to Group 1 or Group 2. You will have an equal chance of being in either group. If you are in Group 1, you will receive routine information before the lung biopsy and you will watch a video on a handheld or laptop machine with headphones. The video is designed to help you understand the biopsy procedure. This video should last about 5 minutes. You will then complete a questionnaire that asks how you feel after watching the video. It will take about 5 minutes to complete. If you are in Group 2, you will receive routine information before the lung biopsy. You will then complete another questionnaire that asks how you feel before the procedure. It will take about 5 minutes to complete. After your routine lung biopsy, both groups will complete a questionnaire that asks how you feel after the procedure. It will take about 5 minutes to complete. For Group 1, the total time to complete the questionnaires and watch the video will be 20 minutes. For Group 2, the total time to complete the questionnaires will be 15 minutes. Length of Study: Your participation in this study will be over once you complete the questionnaire after your lung biopsy. This is an investigational study. Up to 100 patients will take part in this study. All will be enrolled at M. D. Anderson.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
UT MD Anderson Cancer Center
Houston, Texas, United States
Start Date
August 1, 2010
Primary Completion Date
December 1, 2012
Completion Date
December 1, 2012
Last Updated
February 12, 2013
50
ACTUAL participants
Video
BEHAVIORAL
Questionnaires
BEHAVIORAL
Lead Sponsor
M.D. Anderson Cancer Center
NCT07486219
NCT07336732
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07485114