Expired Study
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New York, New York 10065


This study will compare two ways of having people respond to a questionnaire about health and emotional well-being: on a computer and with paper and pencil. We will see how long it takes using both methods. We will also ask you how you feel about using a computer to answer the questions.

Study summary:

To determine feasibility of using the Computer Assisted Survivor Screening (CASS) as a routine screening measure for the survivor population. Specifically, to determine patient acceptance, time to completion, and burden associated with the CASS. To examine the potential utility of the CASS as a routine screening measure in the survivor population. To validate the CASS against the SCL-90-R screening measure. Calculate the sensitivity,specificity, positive and negative predictive values, diagnostic agreement and ROC curve of the CASS compared to the SCL-90. Determine the optimal cut-off scores to optimize agreement between the CASS and the SCL-90.


Inclusion Criteria: - Currently at least 18 years of age and not older than 49 years of age - Diagnosed with first malignancy before the age of 22 - Completed all cancer treatment at least three years prior - Able to complete the survey instruments in English - Scheduled for a routine off-treatment follow-up oncology appointment - Currently disease-free and not receiving any cancer treatment Exclusion Criteria: - History of a central nervous system tumor - A sensory or cognitive impairment that would interfere with completion of the survey - Currently undergoing treatment by a psychiatrist or psychologist (ie., currently receiving psychotherapy and/or psychotropic medications, as per self-report)



Primary Contact:

Principal Investigator
Jennifer Ford, PhD
Memorial Sloan-Kettering Cancer Center

Backup Contact:


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: March 16, 2018

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