Contraceptive Choice at the Time of Uterine Evacuation

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

234 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-31

Study Completion Date

2017-04-30

Brief Summary

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The goal of this project is to investigate whether a pre-visit telephone intervention could increase awareness of long-acting reversible contraception (LARC) availability at the time of uterine evacuation.

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Detailed Description

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Conditions

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Contraception

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Intervention Message

Participants who are randomized to the intervention message will receive contraception information in advance of their appointment that may be helpful in their decision-making.

Group Type EXPERIMENTAL

Telephone message

Intervention Type OTHER

A pre-visit telephone intervention describing availability of long-acting reversible contraceptives at time of uterine evacuation

Control Message

Participants who are randomized to the control message will receive appointment logistic information that may be a helpful reminder.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Telephone message

A pre-visit telephone intervention describing availability of long-acting reversible contraceptives at time of uterine evacuation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age 18 or older
* Scheduled for uterine evacuation
* Speaks English proficiently in order to understand the telephone conversation and the survey questions.