Palliative Care and Symptom Management for the Pediatric Oncology Patient
NCT00675467 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 13
Last updated 2016-04-08
Summary
The goal of this study is to learn about the communication, decision-making, symptom management, emotional adjustment, and spiritual needs of parents and pediatric patients treated at the Children's Cancer Hospital at M. D. Anderson (MCACC).
Primary Objectives:
1. Determine the palliative care service needs of pediatric cancer patients and their parents, including communication, decision-making, symptom management, emotional and spiritual support when receiving treatment for early cancer, treatment for advanced disease, and treatment in the end-of-life period.
2. Identify intra-group differences in the categories listed in Objective 1 for pediatric cancer patients receiving treatment (a) for early cancer, (b) for advanced disease, and (c) at end-of-life.
Secondary Objectives:
1\. Inform the development of a Pediatric Palliative Care Program at the Children's Cancer Hospital at The University of Texas M. D. Anderson Cancer Center (MCACC or MDACC) based on identified needs as determined by primary study aims 1 and 2.
Conditions
- Pediatric Cancers
Interventions
- BEHAVIORAL
-
Focus Group - Parent/Caregiver
A 1 1/2 hour group session with other parents/caregivers.
- BEHAVIORAL
-
Focus Group - Pediatric Patient
A 1 1/2 hour group session with other pediatric patients.
Sponsors & Collaborators
-
M.D. Anderson Cancer Center
lead OTHER
Principal Investigators
-
Rhonda Robert, PhD · M.D. Anderson Cancer Center
Eligibility
- Min Age
- 10 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-04-30
- Primary Completion
- 2016-04-30
Countries
- United States
Study Locations
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