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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01945385
Other study ID # 13-0185
Secondary ID
Status Completed
Phase N/A
First received July 29, 2013
Last updated July 25, 2014
Start date June 2013
Est. completion date September 2013

Study information

Verified date July 2014
Source University of Chicago
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Primary: To compare rates of immediate postabortal LARC uptake between women exposed to a brief, theory-based, video intervention prior to standard contraceptive counseling and women exposed to standard counseling alone.

Secondary: To identify predictors of immediate postabortal LARC uptake among all participants including the role of:

- Demographic and reproductive health history variables

- Baseline decisional balance, self-efficacy and stage of change for contraceptive initiation


Description:

This is a randomized controlled trial evaluating the effect of a brief video intervention on postabortal uptake of long acting reversible contraception.


Recruitment information / eligibility

Status Completed
Enrollment 193
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 29 Years
Eligibility Inclusion Criteria:

- Ages 18 - 29 Surgical abortion being performed the day of the study English speaking

Exclusion Criteria:

- Nonviable pregnancy Sexual assault Administered sedative medication Non English speaking

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
Video intervention
Brief 7 minute video of physician describing LARC methods followed by two patient testimonials about their own postabortal LARC experience.

Locations

Country Name City State
United States Planned Parenthood Near North Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
University of Chicago Society of Family Planning

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postabortal LARC uptake Immediate uptake of IUD or contraceptive implant following surgical abortion Immediate No
Secondary Perceived self efficacy surrounding LARC decision making Subject's own perception of her ability to uptake LARC in the postabortal period. Baseline No
Secondary Perceived decisional balance surrounding LARC decision making Subjects perceived pros and cons around starting a LARC method in the postabortal period Immediate No
Secondary Stage of behavioral change around LARC uptake Immediate No
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