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Clinical Trial Summary

The purpose of this study is to help adolescents and young adult cancer survivors address their psycho-social needs during the transitional period. The transitional period begins at completion of cancer treatment and continues throughout that first year. Patients often report this period can be difficult and distressing in many areas of life. This study will use a simple tool to measure, on a regular basis, the level of distress a young adult may be feeling. Based on this assessment additional mental health support and intervention can be recommended to help cancer survivors cope and enhance their feelings of well-being.


Clinical Trial Description

Study Objective: To establish a successful distress based intervention program for adolescent and young adult survivors in the transition period. Study Design and Methods: The type of design for this study is a feasibility pilot study with repeated measure, within group quantitative design. There is no randomization for this study. The patient will be assessed; at baseline, upon completion of therapy, and at regular three month intervals for the first year, for a total of five assessments. After receiving a referral a member of the AYAST team will contact the patient and set up the initial visit. ;


Study Design


Related Conditions & MeSH terms

  • Adolescent and Young Adult Cancer

NCT number NCT02948712
Study type Interventional
Source Case Comprehensive Cancer Center
Contact
Status Terminated
Phase N/A
Start date February 7, 2017
Completion date June 22, 2022