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Questionnaires and Cognitive Assessments Following Mammography

NCT03412370 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 6

Last updated 2019-01-25

No results posted yet for this study

Summary

This pilot research trial studies how well questionnaires and cognitive assessments work in tracking patient symptoms following mammography. Gathering information over time through questionnaires and cognitive tests about symptoms patients may experience after a mammogram may help doctors understand the cause of these symptoms.

Conditions

  • Health Status Unknown

Interventions

OTHER

Cognitive Assessment

Complete cognitive assessments

OTHER

Questionnaire Administration

Complete questionnaires

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • University of Southern California

    lead OTHER

Principal Investigators

  • Joan Broderick, Ph.D. · University of Southern California

Eligibility

Min Age
21 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-07-27
Primary Completion
2017-09-21
Completion
2017-09-21

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03412370 on ClinicalTrials.gov