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Clinical Trials/NCT00832325
NCT00832325
Active, Not Recruiting
N/A

Adolescent and Young Adult Cancer Survivors: Identity Development

Memorial Sloan Kettering Cancer Center1 site in 1 country300 target enrollmentJanuary 1, 2009

Overview

Phase
N/A
Intervention
interview
Conditions
Cancer
Sponsor
Memorial Sloan Kettering Cancer Center
Enrollment
300
Locations
1
Primary Endpoint
Conduct a comprehensive qualitative assessment through individual interviews and focus groups of identity development, peer and family relationships, and psychosocial concerns among survivors diagnosed during adolescence.
Status
Active, Not Recruiting
Last Updated
2 months ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
January 1, 2009
End Date
January 1, 2027
Last Updated
2 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility 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.

Arms & Interventions

1 individual interviews

The patient will be asked to come in to the Counseling Center at MSKCC (641 Lexington Avenue, 7th Floor) and participate in an individual interview at their convenience.

Intervention: interview

2 Focus Groups

The patient will be asked to come in to the Counseling Center at MSKCC (641 Lexington Avenue, 7th Floor) and participate in a focus group at their convenience.

Intervention: Focus groups

3 Questionnaire

The patient will be asked to participate in three 60-90 minute telephone interviews scheduled at their convenience.

Intervention: Questionnaire

Outcomes

Primary Outcomes

Conduct a comprehensive qualitative assessment through individual interviews and focus groups of identity development, peer and family relationships, and psychosocial concerns among survivors diagnosed during adolescence.

Time Frame: 3 years

Secondary Outcomes

  • Conduct a prospective longitudinal assessment of identity development and peer and family relationships among survivors diagnosed during adolescence.(3 years)

Study Sites (1)

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