This study is currently not recruiting participants.

A prospective study of immediate postpartum contraceptive decision-making and outcomes

Study on Immediate Postpartum Contraception Requests

Not Recruiting
100 years or below
All
Phase N/A
1 Location

Brief description of study.

The purpose of this study is to assess the population of patients who express a desire for immediate postpartum contraception in the form of DepoProvera, Nexplanon, and progestin intrauterine device. The study will evaluate those study participants whose requests are unfulfilled and will determine primary reasons for unfulfilled requests via a patient survey.

Detailed description of study

The purpose of this study is to assess the population of patients who express a desire for immediate postpartum contraception in the form of DepoProvera, Nexplanon, and progestin intrauterine device. The study will evaluate those study participants whose requests are unfulfilled and will determine primary reasons for unfulfilled requests via a patient survey.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: healthy
  • Age: 100 years or below
  • Gender: All

This study investigates the desire for immediate postpartum contraception among patients. It focuses on understanding the demand for methods such as injectables, implants, and intrauterine devices, which are forms of birth control used shortly after childbirth.

Participants will take part in surveys to determine why some requests for these contraceptive methods are not fulfilled. This involves collecting data on patient experiences and any barriers they face in obtaining their preferred contraception.

  • Who can participate: Participants must be postpartum individuals seeking contraception. Specific eligibility criteria such as age or other factors are not detailed in the provided information.
  • Study details: Participants will complete surveys to provide information on their experiences and challenges in obtaining postpartum contraception.
Updated on 19 Feb 2024. Study ID: 1607670376

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