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Clinical Trial Summary

The primary purpose of this study is to assess the psychosocial burden in women who have experienced an abnormal pap results after screening interventions.


Clinical Trial Description

This study will be a Thailand, clinic-based, cross-sectional, questionnaire study. Approximately 151 female participants will be enrolled. Study staff will interview the subject to collect basis demographic data and self reported medical history. And the subjects will be given the questionnaire packet for self-administration. After subjects complete the packet, study staff will review the questionnaires for completeness prior to the study subject leaving the clinic. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00520117
Study type Observational
Source Mahidol University
Contact
Status Completed
Phase
Start date June 2007
Completion date June 2008

See also
  Status Clinical Trial Phase
Active, not recruiting NCT00755599 - Eisenhower's Alternative Speculum Examination N/A