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Clinical Trials/NCT03214848
NCT03214848
Completed
Not Applicable

Evaluation of an Intervention to Increase Post-abortion LARC Uptake: A Randomized Controlled Trial of Educational and Financial Counseling Prior to Clinical Presentation.

Emory University1 site in 1 country1,314 target enrollmentSeptember 13, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post Abortion Contraception
Sponsor
Emory University
Enrollment
1314
Locations
1
Primary Endpoint
Proportion of Long-Acting Reversible Contraception (LARC) methods inserted immediately post abortion in the intervention and standard of care arms.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This is a randomized prospective study evaluating the impact of a brief contraceptive education intervention with optional referral for financial counseling on post abortion long-acting reversible contraceptive (LARC) uptake and contraceptive use at three months post abortion.

Detailed Description

As repeat unintended pregnancy and abortion remain public health challenges, increasing long-acting reversible contraceptive (LARC), specifically intrauterine device (IUD) and contraceptive implant, use among women presenting for abortion care is a priority. Despite its efficacy and safety, LARC methods remain underutilized in the abortion setting. This is a randomized prospective study evaluating the impact of a brief contraceptive education intervention with optional referral for financial counseling on post abortion long-acting reversible contraceptive (LARC) uptake and contraceptive use at three months post abortion.

Registry
clinicaltrials.gov
Start Date
September 13, 2017
End Date
February 21, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lisa Haddad

Assistant Professor

Emory University

Eligibility Criteria

Inclusion Criteria

  • Women calling to schedule an appointment for an abortion and/or those who receive abortion services at the Atlanta Women's Center with fluency in English and able to provide informed consent
  • 16 years and older

Exclusion Criteria

  • Younger than 16 years old

Outcomes

Primary Outcomes

Proportion of Long-Acting Reversible Contraception (LARC) methods inserted immediately post abortion in the intervention and standard of care arms.

Time Frame: Immidiately post abortion (day of the procedure).

Proportion of LARC methods inserted immediately post abortion in the intervention and standard of care arms will be calculated based on data abstracted from patients' medical records.

Secondary Outcomes

  • Proportion of Long-Acting Reversible Contraception (LARC) methods used in the intervention and standard of care arms three months post abortion.(Three months post abortion.)
  • Cost-effectiveness analysis of the study intervention.(Three months post abortion.)

Study Sites (1)

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