Natural Procreative Technology Evaluation and Surveillance of Treatment for Infertility and Miscarriage

This is a prospective cohort observational study. Couples presenting for possible treatment with NPT will be recruited for participation in the study. No randomization will occur. If a couple agrees to participate, investigators will collect information in three ways:

• Questionnaires. (standard of care) These will be done at entry (SOC) to the study, on an annual basis for up to three years (research related), for any pregnancy, or whenever a patient exits the study. Questionnaires may be done by mail, email, or telephone. Each questionnaire has a woman's and a man's version, except the pregnancy questionnaire, which only has a woman's version. Each questionnaire will take approximately 30-45 minutes to complete.
• The subject's own Creighton Model fertility charts. (standard of care)
• Information about NPT treatment and pregnancies from the medical records of their NPT physician(s). (standard of care)

Inclusion criteria

• Couple or women, seeking NPT treatment or consultation to achieve pregnancy, to maintain pregnancy, or for fertility-related health issues.
• Couple or women who is seeking pregnancy WITHIN the coming year.

Exclusion criteria

• Couple or women is not a candidate for NPT for pregnancy (for example, couple or women is medically sterile or medically too high risk for pregnancy).
• Couple or women is not able to provide informed consent (for example, language barriers).