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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00588211
Other study ID # 01-121
Secondary ID CA93182
Status Completed
Phase
First received
Last updated
Start date September 2001
Est. completion date September 13, 2022

Study information

Verified date September 2022
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to develop an accurate way of measuring people's thoughts about cancer risk. The researchers at the Queens Hospital Center, Memorial Sloan-Kettering Cancer Center and Adelphi University are working together to design a new measure. Findings from this study will help us find new ways to help people avoid cancer.


Description:

The goal of the study is to develop and provide initial evidence for the reliability and validity of a measure of cancer-related risk perception. As such, the primary outcomes of the study will be initial construct validity (convergent validity and discriminant validity) of the proposed scale as evidenced by correlations of this test with other tests that vary in the degree of association to the proposed construct of cancer-related risk perception. It is anticipated that the cancer-related risk perception scale will correlate most highly (.50-.60) with measures of tobacco and environmental risk exposures, readiness to quit smoking, and family cancer history.


Recruitment information / eligibility

Status Completed
Enrollment 1514
Est. completion date September 13, 2022
Est. primary completion date September 13, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Subject must be >= to 18 years of age - For recruitment at Adelphi University: Speak English - For recruitment at Queens Hospital Center: Speak English - For recruitment at Queens Hospital Center: Must be a Queens Hospital Center Patient Exclusion Criteria: - Patients who have a history of colorectal cancer at the Queens Hospital Center - Patients who cannot give informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Interviews
45-minute individual interviews after the conclusion of their dental appointment
focus group
A focus group of the preliminary cancer-related risk perception item pool.
Survey
Quantitative item analysis of the final item pool.
Survey
A second confirmatory factor analysis.

Locations

Country Name City State
United States Queens Hospital Center Jamaica New York
United States Adelphi University New York New York
United States Memorial Sloan-Kettering Cancer Center New York New York
United States New York University, College of Dentistry New York New York

Sponsors (4)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center Adelphi University, National Cancer Institute (NCI), Queen's Hospital Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Develop a comprehensive "blueprint," or description of the cancer-related risk perception construct; to use it to generate a cancer-related risk perception item pool; conduct an analysis of the generated items 3 years
Secondary to establish initial evidence for scale reliability and validity 3 years
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