Perception of Palliative Care Encounter
Perception of the Palliative Care Encounter by Patients Who Are Referred to Outpatient Supportive/ Palliative Care
2 other identifiers
observational
209
1 country
1
Brief Summary
Objectives: Primary Objective The primary objective is to determine patients' perceptions of the timeliness of their referral to an outpatient palliative care clinic. The secondary objectives are to determine:
- 1.The factors and variables associated with perception of timeliness such as age, gender, and symptom distress
- 2.The patients' perceptions of the physical environment of the outpatient clinic at UT MD Anderson Cancer Center (UTMDACC) such as lighting, music, and lack of a waiting room; and
- 3.If there is an association between level of distress (physical, psychological, and spiritual distress as measured by Edmonton Symptom Assessment Scale (ESAS) and the usefulness of the referral to palliative care center.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2015
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 16, 2015
CompletedFirst Submitted
Initial submission to the registry
September 22, 2015
CompletedFirst Posted
Study publicly available on registry
September 23, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 7, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
April 7, 2021
CompletedApril 14, 2021
April 1, 2021
5.6 years
September 22, 2015
April 13, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Participants' Perceptions of Timeliness of Referral to an Outpatient Palliative Care Clinic
Percentage of respondents who report that their referral to supportive care was late (including "late" and "too late") estimated with a standard error not larger than 0.04.
1 day
Study Arms (1)
Palliative Care Survey
Initial consultation visit followed by phone survey within 1 week +/- 4 days of initial consultation.
Interventions
Participants complete palliative care survey within 1 week +/- 4 days of initial consultation via phone survey conducted by Research nurse/assistant.
Eligibility Criteria
Participants who have undergone a consultation with a supportive Care doctor in the Supportive Care Center at The University of Texas MD Anderson Cancer Center in Houston, Texas.
You may qualify if:
- Have advanced cancer, defined as locally advanced, metastatic or incurable disease
- \>/=18 years of age
- Seen at UTMDACC outpatient Supportive Care Center for consultation
- Provided informed consent
You may not qualify if:
- Memorial Delirium Assessment Scale (MDAS) \>/= 13.
- Inability to read and speak English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Texas MD Anderson Cancer Center
Houston, Texas, 77030, United States
Related Links
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Angelique N. Wong, MD
M.D. Anderson Cancer Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 22, 2015
First Posted
September 23, 2015
Study Start
August 16, 2015
Primary Completion
April 7, 2021
Study Completion
April 7, 2021
Last Updated
April 14, 2021
Record last verified: 2021-04