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NCT01199952 · ClinicalTrials.gov registry record · NA
RCT: Can a Single Counseling Phone Call Improve Contraception After an Abortion?
A NA study, sponsored by University of California, San Francisco.
- Completed
- Registry status
- NA
- Development phase
- 207
- Enrollment target
NCT01199952 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 207 participants.
The verdict
NCT01199952, a NA study, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- NA
- Development phase
- 207 participants
- Enrollment target
Study Summary
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.
Interventions
- BEHAVIORAL Treatment group: receives counseling phone call intervention
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 207 participants |
| Start Date | 2011-03-21 |
| Est. Completion | 2013-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01199952
The ClinicalTrials.gov registry entry for NCT01199952 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 207 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Treatment group: receives counseling phone call intervention is the first listed.
NCT01199952 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01199952 about?
NCT01199952 is a clinical study titled "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 recei...
What is the current status of trial NCT01199952?
This trial is currently completed. It is a NA study. The enrollment target is 207 participants. The study started on 2011-03-21. Estimated completion is 2013-01.
What interventions are being tested in trial NCT01199952?
The interventions under investigation include: Treatment group: receives counseling phone call intervention (BEHAVIORAL).
Who is sponsoring clinical trial NCT01199952?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
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