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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ACTIVE_NOT_RECRUITING
50 participants
OBSERVATIONAL
2025-08-01
2031-01-01
Brief Summary
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Detailed Description
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To explore the barriers and fears related to use of opioids among a population of adult outpatients with advanced cancer who continue to experience pain after receiving a prescription for opioid analgesia.
Secondary Objective:
To examine associations among opiophobia, anxiety, depression, pain intensity, pain interference, and opioid medication adherence among adults with advanced cancer who report undermanaged pain during the first week after receiving a prescription for an opioid analgesic.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Pain is the documented reason for the Supportive Care consultation
3. Have a prescription for an opioid analgesic
4. Able to read, speak, and consent in English.
Exclusion Criteria
2. Do not have a prescription for an opioid analgesic
3. Individuals for whom there is documentation of inability to provide consent in the medical record
4. Women who are pregnant
5. Patients with a substance use disorder (including alcohol use disorder and excluding tobacco use disorder) documented in the electronic health record under History of Present Illness or in the Medical History.
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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Eileen Hacker, PHD, RN
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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The University of Texas M. D. Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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MD Anderson Cancer Center Website
Other Identifiers
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NCI-2025-05283
Identifier Type: OTHER
Identifier Source: secondary_id
2025-0177
Identifier Type: -
Identifier Source: org_study_id
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