Trial Information
"Evaluation of Clinical Outcomes and Costs of a Transferable Interdisciplinary Lifestyle Intervention Pre- and Per-pregnancy in Obese Infertile Women"
Inclusion Criteria:
- Obese (BMI ≥ 30kg/m2) infertile women
- Overweight (BMI ≥ 27kg/m2) infertile women with polycystic ovary syndrome
Exclusion Criteria:
- Women older than 40 years old
- Women who went through bariatric surgery
- Women under IVF
- Women for whome IVF is the only recommended treatment
- Women who do not speak french
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
Outcome Measure:
Rates of live birth
Outcome Time Frame:
Participants who will become pregnant: for the duration before they get pregnant and up to the end of pregnancy, an expected average of 18 months. Participants who will not become pregnant: 18 months
Safety Issue:
No
Principal Investigator
Jean-Patrice Baillargeon, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Universitaire de Sherbrooke
Authority:
Canada: Health Canada
Study ID:
CIHR/FRN-114125
NCT ID:
NCT01483612
Start Date:
November 2011
Completion Date:
March 2014
Related Keywords:
- Female Infertility
- Polycystic Ovary Syndrome
- Obesity
- Body Weight
- Female
- Infertility, Female/therapy
- Infertility, Female/physiopathology
- Obesity/physiopathology
- Polycystic ovary syndrome
- Pregnancy
- Pregnancy Outcome
- Weight Loss
- Infertility
- Infertility, Female
- Obesity
- Polycystic Ovary Syndrome