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N/A Completed N=341 Randomized Double-blind Prevention

Intervention to Improve Follow-up of Abnormal Pap Test

Source: ClinicalTrials.gov NCT00575510 ↗
Enrolled (actual)
341
Serious AEs
0.0%
Results posted
Aug 2014
Primary outcomePrimary: Adherence to Initial Follow-up (Yes/no) — 60; 54; 58 percentage of patients who were adherent

Summary

This project will examine whether a theory-based telephone intervention delivered by a nurse at the time women are informed of an abnormal Pap test result will increase adherence to follow-up recommendations.

Outcome Measures

OutcomeResultp-value
PRIMARY
Adherence to Initial Follow-up (Yes/no)
60; 54; 58
SECONDARY
State Trait Anxiety Inventory (STAI)-State Scale
12; 11; 11

Eligibility Criteria

Inclusion Criteria

  • Women aged 18 to 55 years who present to the University of Texas Medical Branch (UTMB) clinics for Pap testing.

Exclusion Criteria

  • Women who are currently pregnant
  • Have a current diagnosis of cervical cancer; or
  • Who are unable to understand English or Spanish.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00575510). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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