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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00520117

Enrollment

151

Registered

2007-08-23

Start date

2007-06-30

Completion date

2008-06-30

Last updated

2019-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Papanicolaou Smear

Brief 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.

Detailed 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.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 45 Years

Healthy volunteers

Yes

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.

Design outcomes

Primary

Measure	Time frame
psychological burden of women with abnormal pap-smear	3 months

Countries

Thailand

Outcome results