Preference of Room Setting and Waiting Time in Patients With Advanced, Locally Advanced, or Metastatic Cancer and Their Caregivers Who Are Seen in the Outpatient Supportive/Palliative Care Center
NCT ID: NCT03671226
Last Updated: 2025-10-14
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
NA
406 participants
INTERVENTIONAL
2018-09-28
2027-12-31
Brief Summary
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Detailed Description
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I. To determine patients and caregivers preferences regarding the rooming process in outpatient supportive palliative care clinic, measured by the preference to exam room versus waiting area.
SECONDARY OBJECTIVES:
I. Patients and caregiver perceptions regarding room setting and waiting time in the outpatient supportive care clinic.
II. Extent/experience of team contact in the outpatient supportive care clinic. III. The factors associated with rooming preferences such as age, gender, symptom distress and performance status.
IV. The association between level of distress (physical, psychological, and spiritual distress as measured by Edmonton Symptom Assessment Scale (ESAS) and perception of usefulness of the visit to palliative care center.
V. The attitudes and beliefs toward usefulness of referral to outpatient palliative care.
VI. The correlation between the patient and caregivers preferences.
OUTLINE:
Patients and their caregivers complete a questionnaire over 15 minutes either in person or over the phone within 3 days after their supportive care center visit.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Supportive Care (questionnaire)
Patients and their caregivers complete a questionnaire over 15 minutes either in person or over the phone within 3 days after their supportive care center visit.
Questionnaire Administration
Given questionnaire
Interventions
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Questionnaire Administration
Given questionnaire
Eligibility Criteria
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Inclusion Criteria
* Patient: Seen at University of Texas M. D. Anderson Cancer Center (UTMDACC) outpatient Supportive Care Center for consultation (first visit).
* Patient: Provided informed consent.
* Patient: Can read and speak English or Spanish.
* Patient: Has a consenting caregiver at the time of the Supportive Care consultation visit.
* Caregiver: Provided informed consent.
* Caregiver: Can read and speak English or Spanish.
* Caregiver: Must be with consenting patient at the time of the Supportive Care consultation visit.
Exclusion Criteria
* Patient: Inability to read and speak English or Spanish.
* Patient: No caregiver at the time of Supportive Care consultation visit.
* Caregiver: Inability to read and speak English or Spanish.
18 Years
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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MarieBerta Vidal
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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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-2018-01877
Identifier Type: REGISTRY
Identifier Source: secondary_id
2018-0573
Identifier Type: OTHER
Identifier Source: secondary_id
2018-0573
Identifier Type: -
Identifier Source: org_study_id
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