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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01024166 |
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Date of registration:
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30/11/2009 |
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Primary sponsor: |
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Public title:
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Patient-Reported Outcomes-Based Palliative and Hospice Care Practice: A Usability Study
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Scientific title:
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A Usability Study of Patient-Reported Outcomes (PRO)-Based Palliative and Hospice Care Practice: Integrating PROs and Decision Support Into an Electronic Record |
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Date of first enrolment:
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November 2009 |
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Target sample size:
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18 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01024166 |
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Study type:
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Observational |
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Study design:
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Time Perspective: Prospective
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Countries of recruitment
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United States
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Contacts
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Name:
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Michael A. Kallen, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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UT MD Anderson Cancer Center |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. All patient/caregiver participants will be adults 21 years of age or older.
2. Participants will be palliative care cancer patients and/or their designated
caregivers.
3. Participating patients should be receiving palliative care at the MD Anderson Cancer
Center as an inpatient or have attended at least one outpatient appointment;
participating caregivers should have provided care to their patient during an
inpatient stay or have attended at least one outpatient appointment with their
patient.
4. Physicians and nurses who are experts in palliative care will be eligible for study
participation. For this study's purposes, a physician or nurse with a minimum of four
years of experience working in a palliative care setting will be considered an expert
in palliative care.
Exclusion Criteria:
1. Patients or caregivers who are not able to report on symptom status using the
electronic measurement system.
2. Patient, caregivers, physicians, or nurses who do not agree to sign the study's
informed consent documents.
Age minimum:
21 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Advanced Cancers
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Intervention(s)
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Behavioral: Questionnaire and Review Session
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Primary Outcome(s)
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Evaluation of System Usability of the Prototype Solution (Questionnaire Responses)
[Time Frame: Single assessment point]
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Secondary ID(s)
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2009-0776
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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