Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:24 AM
Ignite Modification Date:
2025-12-25 @ 12:24 AM
NCT ID:
NCT01216358
Eligibility Criteria:
Inclusion Criteria:
* Proficiency in English
* Medically eligible for her chosen form of contraception per standard PPLM clinic protocol
* (For Study Arm A) Desire initiation of an estrogen/progesterone contraceptive method at time of clinic presentation and evaluation
* (For Study Arm B) Desire initiation of a progesterone only contraceptive method at time of clinic presentation and evaluation
* (For Control Arm) Initiating a non-hormonal contraceptive, or not initiating any contraceptive method
* (For Control Arm) Stated intention of not initiating any hormonal contraception over the 3 month study period
* Agreeing to study procedures
Exclusion Criteria:
* Inability to speak and read English
* (For Control Arm) Use of hormonal contraceptive in the past 3 months
* (For Control Arm) Been pregnant in the past 3 months
* States an intention to discontinue use of their newly initiated contraceptive (or lack of contraceptive) before the end of the 3 month study period
* Unwilling or unable to comply with study follow-up procedures
* Inability to give informed consent
* Previous participation in this study
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT01216358
Study Brief:
Protocol Section:
NCT01216358