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Clinical Trials/NCT00579631
NCT00579631
Completed
N/A

Health Behaviors in Adolescent Survivors of Cancer or Similar Illnesses

Memorial Sloan Kettering Cancer Center1 site in 1 country148 target enrollmentJune 22, 2004

Overview

Phase
N/A
Intervention
Not specified
Conditions
Adolescent Cancer Survivors
Sponsor
Memorial Sloan Kettering Cancer Center
Enrollment
148
Locations
1
Primary Endpoint
To describe the patterns of cancer-risk behaviors for adolescent cancer survivors as compared to population-based normative data of "healthy" adolescents, and to describe relevant theory-driven covariates for adolescent cancer survivors.
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to examine the health behaviors of young adults who have been treated for cancer, leukemia, or similar illnesses. We will also ask you some questions about your family members' and friends' health behaviors. We plan to use the findings from this study to design new programs to help teenage cancer survivors resist doing things that might harm their health.

Detailed Description

This study proposes to explore cancer-risk behaviors and future behavioral intentions among adolescent cancer survivors (i.e., 14-19 years old) and compare them to their "healthy" peers using population-based normative data. Additionally, it seeks to determine the significant theory-driven covariates related to adolescent survivors' health behaviors, which will aid in the design of future behavioral interventions.

Registry
clinicaltrials.gov
Start Date
June 22, 2004
End Date
February 8, 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Current age at enrollment between 14 and 19;
  • A diagnosis of cancer between the ages of 8 and 14;
  • At least 12 months post-treatment and no evidence of disease (NED) at the time of assessment;
  • Can be reached by mail or telephone;
  • Fluent in English;
  • Parent or legal guardian able to provide informed consent;
  • Able to provide informed assent.

Exclusion Criteria

  • Major psychopathology or cognitive impairment likely in the judgment of the investigator to interfere with participation and compliance with the protocol.
  • Currently receiving therapy for cancer treatment

Outcomes

Primary Outcomes

To describe the patterns of cancer-risk behaviors for adolescent cancer survivors as compared to population-based normative data of "healthy" adolescents, and to describe relevant theory-driven covariates for adolescent cancer survivors.

Time Frame: conclusion of study

Secondary Outcomes

  • To examine the role and relative utility of sociodemographics, medical characteristics, theory-driven variables in explaining adolescent cancer survivors' health behaviors.(conclusion of study)

Study Sites (1)

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