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Understanding the Psychosocial Needs of Parents Who Have Lost a Child to Cancer
Sponsor: Memorial Sloan Kettering Cancer Center
Summary
The purpose of this study is to understand the experiences and needs of parents who have lost a child to cancer. This will aid us in developing an intervention that may help parents cope with their loss.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
160
Start Date
2009-08
Completion Date
2027-06-02
Last Updated
2025-09-30
Healthy Volunteers
Yes
Conditions
Interventions
Questionnaires/Interviews
Prior to the interview, the measure of prolonged grief disorder symptoms, the PG-13, will be re-administered to participants as a quality assurance check. We will administer 7 self-report measures, which participants can complete in our office, at home, or via telephone, depending on their preferences. These questionnaires should take approximately 75 to 80 minutes to complete. If you are asked to take part in the in-depth interview and you choose to take part, the interview that will take approximately 60 to 90 minutes to complete, depending on the length of the responses to the questions asked. The participant may also be asked if they would be willing to fill out an additional questionnaire about parents' thoughts on the most appropriate timing for raising the topic of a postmortem examination and factors that are important to include in discussions. Despite its importance, autopsy is often not discussed with parents whose child is dying from cancer.
Locations (2)
NCI Clinical Center
Bethesda, Maryland, United States
Memorial Sloan Kettering Cancer Center
New York, New York, United States