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Impact of guidance and consultation management program on women undergoing non-ART infertility treatment

Impact of guidance and consultation management program on women undergoing non-ART infertility treatment - Guidance and consultation management program on non-ART infertility treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027424
Enrollment
310
Registered
2017-07-01
Start date
2017-07-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Women with infertility to receive non-ART infertility treatment

Interventions

Intervention period is six months Three times interventions at the first time, after three months, and after six months We perform the guidance and consultation management program by physician and n

Sponsors

St. Luke's International University Division of Women's Health and Midwifery
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.The women who receive infertility treatment for the first time, and then she is within two years from starting to try pregnancy, and she is under 42 years old at the entry 2.The women who applies non-ART infertility treatment(timing therapy, ovulation induction, artificial insemination) 3.The women who have unknown infertility, or ovulation failure, or polycystic ovary syndrome, or her partner has mild male infertility 4.The women who have complications that will effect slightly on infertility treatment and pregnancy only for follow-up not to need treatment, or who have a history of previous surgery 5.The women who have not experience of both delivery and childrearing 6.The person who can read and write and talk in Japanese

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Japan

Contacts

Public ContactAkiko Mori

St. Luke's International University Division of Women's Health and Midwifery

akiko-mori@slcn.ac.jp+81-3-3543-6391

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026