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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

Caregiver Clinical Trial

Official title:
Perception of Supportive Care Patients and Caregivers Who Are Seen in the Outpatient Supportive/Palliative Care Center Regarding the Preference of Room Setting and Waiting Time

Clinical Trial Summary

This trial studies the preference of room setting and waiting time in patients with cancer that has spread to nearby tissue or lymph nodes or other places in the body and their caregivers who are seen in the outpatient supportive/palliative care center. Room setting preferences of patients and caregivers may help to understand their opinion regarding direct rooming system in the outpatient supportive/palliative care center.

Clinical Trial Description

PRIMARY OBJECTIVES: 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03671226
Study type Interventional
Source M.D. Anderson Cancer Center
Contact
Status Active, not recruiting
Phase N/A
Start date September 28, 2018
Completion date December 31, 2024
View Details
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