Oral Contraception
Conditions
Keywords
oral contraception, hormonal contraception, contraceptive behavior, patient compliance
Brief summary
The purpose of this study is to determine whether getting more packs of birth control pills leads to improved continuation, when compared with getting the traditional supply.
Detailed description
Discontinuation of oral contraceptive use in the initial months is common; successful early continuation is predictive of long term continuation and prevention of unintended pregnancy. The conventional approach to initiation of hormonal contraceptives in publicly funded clinics across the United States is to give the patient a limited supply of OCs, or a prescription with a limited number of refills, and then have her return to the clinic for a refill. This approach requires the patient to make frequent visits to the clinic, a barrier to method continuation. This randomized trial will evaluate a simple but potentially powerful change in family planning clinic practice, i.e., the effect of dispensing more versus fewer cycles of oral contraception (OC). The study will be carried out in an urban, publicly funded family planning clinic that serves a population that is poor, young and primarily Hispanic or AfricanAmerican. This population was targeted as its members are at increased risk of discontinuing contraception in the first year of use.
Interventions
7 packs of pills, or 1 pack of pills and a prescription for 6 refills
3 packs of pills, or 1 pack of pills and a prescription for 2 refills
Sponsors
Study design
Eligibility
Inclusion criteria
* English or Spanish speaker * age less than or equal to 35 years requesting OC as their primary method of contraception * currently sexually active or anticipating sexual activity within the next 30 days
Exclusion criteria
* contraindications to oral contraceptives per clinic protocol (e.g., hypertension and pregnancy) * currently using OCs (that is, current users requesting a routine refill) * desiring pregnancy within the next 6 months * leaving the clinic catchment area within 6 months * previous participation in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| oral contraception continuation | 6 months |
Countries
United States