Status:

COMPLETED

Palliative Care and Symptom Management for the Pediatric Oncology Patient

Lead Sponsor:

M.D. Anderson Cancer Center

Conditions:

Pediatric Cancers

Eligibility:

All Genders

10-18 years

Brief 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 C...

Detailed Description

PARENT: The Focus Group: If you agree to take part in this study, you will attend a 1 1/2 hour group session with 3-9 other caregivers. The group will be led by a group leader and an assistant. The ...

Eligibility Criteria

Inclusion

  • Inclusion for Children:
  • 10-18 years of age
  • MD Anderson Children's Cancer Center (MCACC) cancer patient
  • receiving anti-cancer treatment for disease that is not recurrent or metastatic for cancer diagnosed in the past 3-12 mos or receiving anti-cancer treatment for recurrent or metastatic cancer diagnosed within the past 3-12 months
  • speak \& understand English
  • reside in the Greater Houston area
  • provide IRB-approved pediatric assent or informed consent, as age appropriate
  • if \< 18 years of age, provide Internal Review Board (IRB)-approved parental permission
  • child's eligibility is not contingent upon parent's decision to participate
  • Inclusion for parents:
  • self-identified parent(s) that has(have) a child eligible for study, per the inclusion and exclusion criteria noted above or has had a child (0-18 yrs of age at time of death) treated for cancer at MCACC who has died in the last 1 to 2 years
  • speak and understand English
  • reside in the Houston metropolitan area
  • provide IRB-approved informed consent
  • attend different focus groups if more than one eligible parent per child (max 2 parents per child)
  • parent's eligibility is not contingent upon the child's decision to participate

Exclusion

  • Exclusion for Children:
  • have cognitive impairment, developmental delay, or emotional distress that would limit participation in a group discussion, as determined by the clinical judgment of the investigator
  • younger than 10 years or older than 18 years of age
  • Exclusion for Caregiver:
  • have cognitive impairment, developmental delay, or emotional distress that would limit participation in a group discussion, as determined by the clinical judgment of the investigator.

Key Trial Info

Start Date :

April 1 2008

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

Estimated Enrollment :

13 Patients enrolled

Trial Details

Trial ID

NCT00675467

Start Date

April 1 2008

Last Update

April 8 2016

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University of Texas MD Anderson Cancer Center

Houston, Texas, United States, 77030