None listed
Conditions
Brief summary
The primary purpose of the study is to determine whether women prescibed a twelve month supply rather than the usual four month supply of the combined oral contraceptive pill at initiation of this contraceptive method are more likley to continue this method when followed-up by phone or e-mail twelve months later. The study will also look at womens' preferences for each initiation regimen through administration of a questionnaire. The hypothesis is that women are more likley to continue the contraceptive pill if they are prescribed the longer initiation regimen and will have a preference for this regimen over the shorter four month regimen.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
Women aged 18-40 years who choose this method of contraception and are eligible according to standard World Health Organisation (WHO) criteria to use the combined oral contraceptive pill; have not used it in the past 2 years; are not intending to become pregnant in the next 12-months.
Exclusion criteria
Ineligible for the combined contraceptive pill; outside age criteria; do not consent to randomisation; require an interpreter.