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OpenTrials
Completed

NCT Number: NCT01199952

RCT: Can a Single Counseling Phone Call Improve Contraception After an Abortion?

Hypothesis: Use of an effective contraceptive six weeks after abortion will be higher in the treatment group than in the control group.

Primary Aim ·To determine use of an effective contraceptive method six weeks after abortion in women who choose combined hormonal contraception (CHC) and who receive a three-week educational phone call as compared to women who do not receive the intervention.

Secondary Aims

* To describe the most common concerns and logistical problems women experience with initiating and adhering to CHC after abortion. * To describe the concerns that lead to discontinuation or method change. *To assess feasibility of conducting a follow-up telephone call in this population This is a randomized, controlled trial to assess the effect of a three-week follow-up phone call in women who choose combined hormonal contraception on the day of their abortion at the San Francisco General Hospital Women's Options Center. Subjects randomized to the treatment group will receive an interventional phone call three weeks after their abortion; participants randomized to the control group will not receive the call. All subjects will receive a follow-up call six weeks after their abortion to assess and compare method use between the two groups. Calls will be made at three- and six-weeks post abortion in order to give subjects enough time to initiate CHC and to assess continuation into the second month of the method. Data will be collected at baseline, during the intervention for the treatment group and during the final follow-up call for both groups. The primary outcome is use of an effective contraceptive six weeks after abortion.

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Key information

Conditions

Age range

15 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

San Francisco General Hospital

San Francisco, California, 94110, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women over the age of 15 who choose pill, patch or ring to begin after their abortion
  • Women able and willing to be contacted by phone for up to 2 months after enrollment

Exclusion criteria

  • Women who do not speak and read English or Spanish

Treatment and study plan

Treatment group: receives counseling phone call intervention

Behavioral

Subjects in the treatment arm will receive a phone call from a health educator to assist with contraception, 3 to 4 weeks after enrollment.

Primary outcomes

  1. Number of Participants Using an Effective Contraceptive Method 6 Weeks After Abortion

    Time frame: 6 weeks after abortion procedure

    To determine use of an effective contraceptive method six weeks after abortion in women who choose combined hormonal contraception (CHC) and who receive a three-week educational phone call as compared to women who do not receive the intervention.

Secondary outcomes

  1. Reasons for Discontinuation of Contraception

    Time frame: 6 weeks after abortion procedure

    To describe the most common concerns and logistical problems women experience with initiating and adhering to CHC after abortion.

    To describe the concerns that lead to discontinuation or method change.

    To assess feasibility of conducting a follow-up telephone call in this population

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • Society of Family Planning

Registry information

Official study title

A Randomized Controlled Trial: Contraceptive Counseling After an Abortion

Acronym: PPR

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Sep 13, 2010
Registry last updated
Sep 19, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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