Childhood Cancer Survivor Survey
NCT00788476 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 167
Last updated 2015-01-09
Summary
Objectives:
1. To explore current lifestyle practices, health status, and quality of life among childhood cancer survivors and parent/guardians who are identified as "primary caregivers."
2. To explore childhood cancer survivors' and "primary caregivers'" awareness of future health risks.
3. To explore interest in various lifestyle interventions and delivery channels among childhood cancer survivors and their "primary caregivers."
4. To explore factors which may serve as mediators or moderators of future lifestyle interventions that target childhood cancer survivors and their "primary caregivers," e.g., strength of the caregiver-child bond, geographic distance from one another, and level of education.
Conditions
Interventions
- OTHER
-
Survey
Survey packets to adult (\>18 years old) childhood cancer survivors who return to MDACC for follow-up appointments within the next 12-months and conduct a mailed survey with the remaining participants and their "primary caregivers" i.e. guardians of survivors who are currently under age 18.
Sponsors & Collaborators
-
M.D. Anderson Cancer Center
lead OTHER
Principal Investigators
-
Joann L. Ater, MD, BA · UT MD Anderson Cancer Center
Eligibility
- Min Age
- 8 Years
- Max Age
- 34 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-10-31
- Primary Completion
- 2013-08-31
- Completion
- 2013-08-31
Countries
- United States
Study Locations
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