NCT00579293

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2004

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2004

Completed
3.4 years until next milestone

First Submitted

Initial submission to the registry

December 20, 2007

Completed
4 days until next milestone

First Posted

Study publicly available on registry

December 24, 2007

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2008

Completed
Last Updated

July 28, 2008

Status Verified

July 1, 2008

Enrollment Period

3.9 years

First QC Date

December 20, 2007

Last Update Submit

July 24, 2008

Conditions

Childhood Cancer

Keywords

adult survivor of childhood cancercomputer assisted screening of survivors (CASS)

Eligibility Criteria

Age18 Years - 49 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

adult survivors of childhood cancer

You may qualify if:

  • 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

You may not qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Memorial Sloan-Kettering Cancer Center

New York, New York, 10065, United States

Location

Related Links

MeSH Terms

Conditions

Neoplasms

Study Officials

  • Jennifer Ford, PhD

    Memorial Sloan Kettering Cancer Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

December 20, 2007

First Posted

December 24, 2007

Study Start

August 1, 2004

Primary Completion

July 1, 2008

Study Completion

July 1, 2008

Last Updated

July 28, 2008

Record last verified: 2008-07

Locations

US(1)