A randomised trial of educational interventions for women taking the combined oral contraceptive pill (COCP)

Completed

• Conditions: Pregnancy and childbirth: Pregnancy; Pregnancy and Childbirth; Pregnancy

• Registration Number: ISRCTN22671317
• Lead Sponsor: HS R&D Regional Programme Register - Department of Health (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-01-23
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 0

Inclusion Criteria

Women aged 18-45 years attending check up appointment for repeat prescription of the combined contraceptive pill.

Exclusion Criteria

1. Aged 17 or under, owing to the sensitivity of collecting the postal outcome measures
2. Unable to complete the questionnaire (learning disability, schizophrenia, major current manic or depressive episode, or both)
3. or if the consultation was their first for the contraceptive pill (this created the ethical dilemma of randomising such patients to a control group where they would receive no education on the pill rules)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ot provided at time of registration

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration