Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00807898 · ClinicalTrials.gov registry record

Health Care Decisions for Female Adolescents: The Role of Mothers and Daughters in Decision Making

A clinical trial, sponsored by University of Louisville.

Completed
Registry status
136
Enrollment target

NCT00807898: Completed study, sponsored by University of Louisville.

NCT00807898 is a clinical trial that has completed, run by University of Louisville. The registered enrollment target is 136 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00807898 has completed, sponsored by University of Louisville.

COMPLETED
Registry status
136 participants
Enrollment target

Study Summary

Preventing cervical cancer is a public health concern. Since 2006 a quadrivalent vaccine for young women nine to twenty six years of age has been available to protect against the human papillomavirus (HPV) and to prevent some types of cervical cancer (Gardasil). The vaccine is an important health promotion tool to address the widespread prevalence of HPV and cervical cancer, but not all eligible young women receive the vaccine. The vaccine is most effective when administered to young women before their sexual debut. When the vaccine is given to young women less than 18 years of age, parental permission is required. This permission is usually provided by the young woman's mother. Understanding predictors of a mother's decision for her minor daughter to receive the HPV vaccine will inform interventions that seek to increase the number of young women who receive the vaccine. The study will focus on mothers and their adolescent daughters between 13-17 years of age. We hypothesize that the Expanded Theory of Planned Behavior will explain a mother's decision to choose the HPV vaccine for her daughter. Research Questions include: 1)What TPB variables predict a mother's decision to choose HPV vaccine for her daughter? 2)What variables predict the strength of a daughter's influence on the mother's decision to choose HPV vaccine for her daughter? 3) What are the relationships between the mothers' and daughters' scores on the variables related to the decision to choose HPV vaccine? 4) How do the mothers and daughters who chose to receive the HPV vaccine differ descriptively from those mothers and daughters who do not choose to receive the HPV vaccine?

Trial Details

FieldValue
Enrollment Target 136 participants
Start Date 2009-01
Est. Completion 2011-01
University of Louisville

217 total trials

What the finished NCT00807898 record still lists

NCT00807898 is an observational study that tracks outcomes without assigning an intervention. The registered 136 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT00807898 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00807898 about?

NCT00807898 is a clinical study titled "Health Care Decisions for Female Adolescents: The Role of Mothers and Daughters in Decision Making". Preventing cervical cancer is a public health concern. Since 2006 a quadrivalent vaccine for young women nine to twenty six years of age has been available to protect against the human papillomavirus (HPV) and to prevent some types of cervical cancer (Gardasil). The vaccine is an important health pr...

What is the current status of trial NCT00807898?

This trial is currently completed. The enrollment target is 136 participants. The study started on 2009-01. Estimated completion is 2011-01.

Who is sponsoring clinical trial NCT00807898?

This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01555892 · 136 participants · Phase 1

    Cytotoxic T-Lymphocytes for EBV-positive Lymphoma, GRALE

  • NCT03216525 · 136 participants · Phase 3

    Alvimopan Versus Placebo in Patients Undergoing Radical Cystectomy on an Enhanced Recovery Protocol

  • NCT04476901 · 136 participants · Phase 2

    Administration of Allogeneic-MSC in Patients With Non-Ischemic Dilated Cardiomyopathy

  • NCT04603898 · 136 participants · NA

    Oxalate Formation From Ascorbic Acid

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00807898, the US trial registry maintained by the National Library of Medicine. NCT00807898 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.