Training midwives in the insertion of contraceptive implants to increase uptake in the immediate postpartum period: a feasibility pilot study

Not Applicable

Completed

• Conditions: Public Health - Health service research; nintended pregnancy; Unintended pregnancy; Reproductive Health and Childbirth - Contraception

• Registration Number: ACTRN12618001537246
• Lead Sponsor: Family Planning NSW

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-09-13
• Study Completion: 2021-05-06
• Last Update Posted: 31 January 2022

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

Midwives are the primary participants for this study. Any Registered Midwife practicing in RPAH or Canterbury Hospital postnatal wards, birth centres or and Midwifery Group Practice that has an ongoing minimum workload of one shift per week will be eligible to participate.

Exclusion Criteria

Midwives who do not have regular shifts at the participating hospitals or whose supervisors do not support their participation in the Implanon® NXT insertion training program.

Study & Design

• Study Type: Interventional
• Study Design: Not specified