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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


Clinical Trial Description

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


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01945385
Study type Interventional
Source University of Chicago
Contact
Status Completed
Phase N/A
Start date June 2013
Completion date September 2013

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