Impact of guidance and consultation management program on women undergoing non-ART infertility treatment
Not Applicable
- Conditions
- Women with infertility to receive non-ART infertility treatment
- Registration Number
- JPRN-UMIN000027424
- Lead Sponsor
- St. Luke's International University Division of Women's Health and Midwifery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 310
Inclusion Criteria
Not provided
Exclusion Criteria
1.The women who need in vitro fertilization or micro insemination medically. 2.The women who have already a history of infertility treatment in another hospital. 3.The women who have complications* that need treatment before infertility treatment start or at the same time. *Endometriosis, Uterine myoma, Ovarian cyst, Impaired glucose tolerance, Mental nervous system disease, Cervical zone cytodiagnosis abnormality, Premature ovarian insufficiency 4.The women who have a history of stillbirth or early neonatal death.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Health Related Quality of Life Time of the measurement is at start of treatment, three months later, six months later and 12 months later
- Secondary Outcome Measures
Name Time Method 1.Fertility quality of life. 2.The required time until pregnancy: The days from start of treatment to pregnancy test positive; The number of the treatment cycle. 3.The cost of treatment 4.Drop-out rate from treatment: The patients not visiting a hospital for treatment in reason of patients oneself or reason unknown though they are under treatment. 5.Improvement of the lifestyle and physical function: Decrease of smoking behavior, Decrease of excessive intake of alcohol, Appropriate range of BMI, Improvement of menstrual cycle.