N/A
N=341
Intervention to Improve Follow-up of Abnormal Pap Test
Cervical Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00575510 ↗Enrolled (actual)
341
Serious AEs
0.0%
Results posted
Aug 2014
Primary outcome: Primary: Adherence to Initial Follow-up (Yes/no) — 60; 54; 58 percentage of patients who were adherent
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Intervention (Behavioral); Active control (Behavioral)
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- The University of Texas Medical Branch, Galveston
- Primary completion
- Apr 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Adherence to Initial Follow-up (Yes/no) |
60; 54; 58 | — |
| SECONDARY State Trait Anxiety Inventory (STAI)-State Scale |
12; 11; 11 | — |
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.
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.
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.