Trials Sponsors Conditions Drugs Pricing

Conditions

Post Abortion Contraception

Keywords

Long-acting reversible contraceptivePost AbortionIintrauterine deviceContraceptive implantLARCIUD

Outcome Measures

Primary Outcomes (1)

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

Secondary Outcomes (2)

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 Arms (2)

Standart of Care

NO INTERVENTION

Standard of care at the clinic is to discuss the abortion procedure without specific contraceptive counseling given prior to the day of abortion procedure.

Contraceptive education prior to abortion

EXPERIMENTAL

Addition (to the standard or care) of a brief phone contraceptive education with optional financial counseling referral prior to abortion visit.

Behavioral: Contraceptive education prior to abortion

Interventions

Contraceptive education prior to abortionBehavioral

Contraceptive education script will be delivered over the phone prior to abortion visit.

Contraceptive education prior to abortion

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age16 Years+

Sexfemale(Gender-based eligibility)

Healthy VolunteersNo

Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

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
years and older

Sponsors & Collaborators

Woodruff Health Sciences Center Foundation
Type not reportedcollaborator
Emory University
Otherlead

Study Sites (1)

Atlanta Women's Center

Atlanta, Georgia, 30297, United States

Study Officials

Lisa Haddad, MD
Emory University
PRINCIPAL INVESTIGATOR

Enrollment

1,314 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: not applicable
Allocation: RANDOMIZED
Masking: DOUBLE
Who Masked: INVESTIGATOR, OUTCOMES ASSESSOR
Purpose: PREVENTION
Intervention Model: PARALLEL
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Assistant Professor

Study Record Dates

First Submitted

July 10, 2017

First Posted

July 12, 2017

Study Start

September 13, 2017

Actual (reported)

Evaluation of an Intervention to Increase Post-abortion LARC Uptake.

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (2)

Study Arms (2)

Standart of Care

Contraceptive education prior to abortion

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (2)

Study Arms (2)

Standart of Care

Contraceptive education prior to abortion

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations