Women's Experience of Post-placental Intrauterine Contraception
Research type
Research Study
Full title
Women's experience of immediate post-placental intrauterine contraception in Lothian
IRAS ID
215645
Contact name
Michelle Cooper
Contact email
Sponsor organisation
NHS Lothian
Duration of Study in the UK
0 years, 11 months, 21 days
Research summary
This project is about evaluating the views and experiences of women who have received intrauterine contraception at the time of having their baby within Lothian in order for us to better understand and develop this contraceptive service for the future. This will be achieved through semi-structured interviews carried out by a trained qualitative researcher.
REC name
London - Harrow Research Ethics Committee
REC reference
17/LO/0225
Date of REC Opinion
25 Jan 2017
REC opinion
Favourable Opinion