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

NCT00140296 · ClinicalTrials.gov registry record · NA

Using the Healthcare Visit to Improve Contraceptive Use

A NA study, sponsored by Centers for Disease Control and Prevention.

Completed
Registry status
NA
Development phase
747
Enrollment target

NCT00140296: Completed NA study, sponsored by Centers for Disease Control and Prevention.

NCT00140296 is a NA study that has completed, run by Centers for Disease Control and Prevention. The registered enrollment target is 747 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00140296, a NA study, has completed, sponsored by Centers for Disease Control and Prevention.

COMPLETED
Registry status
NA
Development phase
747 participants
Enrollment target

Study Summary

Consistent and correct use of an effective contraceptive method is a primary determinant in preventing pregnancy. Unfortunately, only a minority of healthcare providers adequately address women's contraceptive needs. We have developed a standardized behavioral-based contraceptive counseling model that can be used by providers and other clinic staff to address this limitation. The model, ESP, is an adaptation of motivational interviewing and involves: Exploring discrepancies between pregnancy intention and contraceptive use and between risk of STDs and condom use; Sharing information; and Promoting behaviors to reduce risk. Study question: Does ESP counseling lead to an increase in consistency and effectiveness of contraceptive use among women at risk of unintended pregnancy? Methods: Randomized controlled trial of 747 women, ages 16-44, at self-identified risk of unintended pregnancy enrolled from March 2003 to September 2004 at healthcare settings in North Carolina. Intervention participants received individualized ESP counseling from a health educator to address barriers to effective and consistent contraceptive use. Risk reduction steps were negotiated. Pregnancy, Chlamydia infection and contraceptive use were assessed at baseline and follow-up. "Highly effective" contraceptive use was defined as a combination of effectiveness and consistency. Women in the control arm received general preventive health counseling (e.g., smoking and exercise). Differences between the study arms at 12-months may illustrate the longer term influence of the intervention.

Interventions

  • BEHAVIORAL Contraceptive counseling

Trial Details

FieldValue
Enrollment Target 747 participants
Start Date 2003-03
Est. Completion 2005-09
Phase NA

What the finished NCT00140296 record still lists

NCT00140296 is an interventional study that assigns participants to a tested intervention. The registered 747 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (47% lower).

The record links to 0 conditions, and to 1 intervention - of which Contraceptive counseling is the first listed.

NCT00140296 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00140296 about?

NCT00140296 is a clinical study titled "Using the Healthcare Visit to Improve Contraceptive Use". Consistent and correct use of an effective contraceptive method is a primary determinant in preventing pregnancy. Unfortunately, only a minority of healthcare providers adequately address women's contraceptive needs. We have developed a standardized behavioral-based contraceptive counseling model th...

What is the current status of trial NCT00140296?

This trial is currently completed. It is a NA study. The enrollment target is 747 participants. The study started on 2003-03. Estimated completion is 2005-09.

What interventions are being tested in trial NCT00140296?

The interventions under investigation include: Contraceptive counseling (BEHAVIORAL).

Who is sponsoring clinical trial NCT00140296?

This trial is sponsored by Centers for Disease Control and Prevention, which has 139 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00140296's enrollment target sits among peer trials

747 145th of 2000 higher than 1,856 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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

  • NCT02048332 · 750 participants · Phase 1

    Donor-Derived Viral Specific T-cells (VSTs)

  • NCT02087852 · 750 participants

    Kidney Cancer DNA Registry

  • NCT02532452 · 750 participants · Phase 2

    Third Party Viral Specific T-cells (VSTs)

  • NCT03126916 · 750 participants · Phase 3

    Testing the Addition of 131I-MIBG or Lorlatinib to Intensive Therapy in People With High-Risk Neuroblastoma (NBL)

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 NCT00140296, the US trial registry maintained by the National Library of Medicine. NCT00140296 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.