Expired Study
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New York, New York 10065


Purpose:

The purpose of this study is to better understand how the illness has affected the identity and what needs the survivor may have. We hope that this information will help us provide better care to future adolescent and young adult cancer survivors.


Criteria:

Inclusion Criteria: - Current age greater than and including 15 and up to and including 25 years of age at time of consent - Diagnosis of a first cancer > or = to 14 and up to and including 21 years of age - At least 6 months post-treatment according to participant's self-report. - Able to provide informed consent (or parent or legal guardian consent and participant assent for those participants under 18 years of age) - Able to speak English. This inclusion criterion is included because study assessments were designed and validated in English and many of them are not currently available in other languages. Translation of questionnaires into other languages would require reestablishing the reliability and validity of these measures. Therefore, participants must be able to communicate in English to complete the assessments. Exclusion Criteria: - Will exclude survivors with severe cognitive impairment that precludes them from being able to give information consent and/or complete the questionnaires.


NCT ID:

NCT00832325


Primary Contact:

Principal Investigator
Marie Barnett, PhD
Memorial Sloan Kettering Cancer Center


Backup Contact:

N/A


Location Contact:

New York, New York 10065
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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