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OpenTrials
Completed

NCT Number: NCT02380781

Contraceptive Counseling in the Postpartum Period

This is a prospective randomized control trial in which we propose an intervention in the immediate post-partum period to educate women about contraceptive options, particularly long acting reversible contraception (LARC) methods with an aim of increasing the amount of women who choose a LARC method.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University Hospitals Case Medical Center

Cleveland, Ohio, 44106, United States

About this study

Eligible participants will be identified in the post-partum period and will be randomized to one of two groups. The control group will receive the standard of care contraceptive counseling which includes any prenatal counseling they received as well as information from the nurse practitioner that rounds on them in the post-partum period. The intervention group will also receive the standard of care contraceptive counseling but will also watch a 10 minute video created by the CHOICE project which counsels on different contraceptive options. Both groups will fill out a pre-intervention questionnaire as well as a post-intervention questionnaire 24hrs later. The primary outcome will be which type of contraception each woman chooses. The secondary outcomes will include determining if the women come to their post-partum visits as well as if they get the method of contraception they chose on the post-partum floor.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women giving birth at University Hospitals Case Medical Center
  • Patient of the Women's Health Center
  • Women delivering only one child
  • Women receiving contraceptive counseling from the nurse practitioner that cares for the postpartum unit

Exclusion criteria

  • Severe neonatal complication at time of delivery (neonatal death, neonatal admission to the neonatal intensive care unit (NICU) except in cases of chorioamnionitis)
  • Severe maternal complication at time of delivery (patient requiring intensive care unit care, patient requiring hysterectomy at time of delivery)
  • Preterm delivery <34 weeks

Treatment and study plan

Information in the form of a video

Behavioral

see intervention description

Primary outcomes

  1. Choice of contraceptive method

    Time frame: 24 hours post-intervention

    Will be obtained through use of a questionnaire.

Secondary outcomes

  1. Return to clinic for postpartum visit

    Time frame: 12 weeks post-intervention

    Will use ambulatory electronic medical record (EMR) to determine if patient returned to clinic for follow up visit.

  2. Obtained desired method of contraception

    Time frame: 12 weeks post-intervention

    Will use ambulatory EMR to determine if patient received her desired method of contraception.

Sponsors and collaborators

Lead sponsor

University Hospitals Cleveland Medical Center

Other

Registry information

Important dates

Study start
2015
Primary completion
2017
Study completion
2018
First posted
Mar 5, 2015
Registry last updated
Jul 6, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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