Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
50 participants
OBSERVATIONAL
2010-08-31
2012-12-31
Brief Summary
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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.
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Detailed Description
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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.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Questionnaires + Video
Video
5 minute multimedia presentation (video)
Questionnaires
Questionnaires
2 questionnaires pre and post procedure taking approximately 15 minutes each to complete.
Interventions
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Video
5 minute multimedia presentation (video)
Questionnaires
2 questionnaires pre and post procedure taking approximately 15 minutes each to complete.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Literate English-speaking
Exclusion Criteria
2. Current diagnosis of psychosis, dementia or other mentally altered state.
3. Monitored anesthesia care (MAC) or general endotracheal anesthesia (GETA) during the procedure.
4. Patients who are clinically diagnosed as hearing and visually impaired.
5. Patients who have had prior image guided biopsies in our department.
18 Years
ALL
No
Sponsors
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M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Stephen McRae, MD
Role: PRINCIPAL_INVESTIGATOR
UT MD Anderson Cancer Center
Locations
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UT MD Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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UT MD Anderson Cancer Center website
Other Identifiers
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2010-0397
Identifier Type: -
Identifier Source: org_study_id
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