Assessing the Psychosocial Burden in Women With an Abnormal Pap Results After Screening Interventions

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

151 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-06-30

Study Completion Date

2008-06-30

Brief Summary

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

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Detailed Description

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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.

Conditions

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Papanicolaou Smear

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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negative pap-smear

No interventions assigned to this group

positive pap-smear

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* female, between 18 and 45 years of age and must have recently experienced an abnormal pap results within the past 3 months.

Exclusion Criteria

* has any condition which in the opinion of the investigator might interfere with the evaluation of the study objectives
* has other concurrent/active STD's
* has a history of known prior vaccination with an HPV vaccine
* has a history of recent (within 1 year from date of enrollment) or ongoing alcohol abuse or other drug abuse.

Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes