Patient is screened for pregnancy intention and then has a bedside family planning counseling session with the investigator taking into account pregnancy intention, medical conditions, medications, and previous contraception used. At the end of the conversation, if patient is desiring contraception, the patient is offered three contraception options (as appropriate for their medical conditions and paid for as part of the study) to be initiated prior to discharge: Etonogestrel implant, medroxyprogesterone 150 mg IM injection, or a year's supply of oral contraception pills.

Patient is given a flyer that recommends they discuss pregnancy intention and contraception with their OB/GYN or primary care physician.

Patients receive a deception consent so as not to influence them by the consent process. Consent states that the purpose of the project is to study patterns of birth control usage of women admitted to the hospital. Patient is not given any further intervention.

Bedside pregnancy intention screening and family planning counseling with offer of bedside contraception initiation.

Number of patients using contraception 3 months post discharge as ascertained by telephone interview.

Number of pregnancies 3 months post discharge as ascertained by telephone interview.

Number of patient using contraception 12 months post discharge as ascertained by telephone interview.

Number of pregnancies 12 months post discharge as ascertained by telephone interview.

Percent of study population using contraception at time of screening

Percentage of patients where the electronic medical record was inaccurate regarding patient's contraception usage