Evaluation of Clinical Outcomes and Costs of a Lifestyle Intervention in Obese Infertile Women (OF)
Primary Purpose
Female Infertility, Polycystic Ovary Syndrome, Obesity
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Interdisciplinary lifestyle intervention
Sponsored by
About this trial
This is an interventional health services research trial for Female Infertility focused on measuring Body Weight, Female, Infertility, Female/therapy, Infertility, Female/physiopathology, Obesity/physiopathology, Polycystic ovary syndrome, Pregnancy, Pregnancy Outcome, Weight Loss
Eligibility Criteria
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
Sites / Locations
- Centre hospitalier universitaire de Sherbrooke
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Lifestyle counseling
control
Arm Description
Outcomes
Primary Outcome Measures
Rates of live birth
Secondary Outcome Measures
Fertility outcomes
Pregnancy outcomes
Neonatal outcomes
Clinical outcomes
Evolution of anthropometric measures, change in lifestyle habits, physical fitness level and evolution of readiness for change.
Cost per life birth, and other measures of cost-effectiveness
All costs (interventions and complications) to achieve one life birth, including either all women with a life birth or all enrolled women (by intervention arm).
Clinical outcomes in male partners
Evolution of anthropometric measures and change in lifestyle habits in male partners.
Clinical outcomes of female participants
Evolution of anthropometric measures, changes in lifestyle habits (diet, exercise, alcohol, tobacco), physical fitness level, evolution of readiness for change, etc.
Full Information
NCT ID
NCT01483612
First Posted
November 25, 2011
Last Updated
February 1, 2023
Sponsor
Université de Sherbrooke
Collaborators
Canadian Institutes of Health Research (CIHR), Ministere de la Sante et des Services Sociaux
1. Study Identification
Unique Protocol Identification Number
NCT01483612
Brief Title
Evaluation of Clinical Outcomes and Costs of a Lifestyle Intervention in Obese Infertile Women
Acronym
OF
Official Title
"Evaluation of Clinical Outcomes and Costs of a Transferable Interdisciplinary Lifestyle Intervention Pre- and Per-pregnancy in Obese Infertile Women"
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
January 20, 2012 (Actual)
Primary Completion Date
August 2018 (Actual)
Study Completion Date
August 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Université de Sherbrooke
Collaborators
Canadian Institutes of Health Research (CIHR), Ministere de la Sante et des Services Sociaux
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
BACKGROUND: Obesity increases the risk of polycystic ovary syndrome (PCOS), characterized by anovulatory cycles, but it is also associated with reduced fertility even in ovulatory women. Moreover, obesity increases the costs of assisted human reproduction (AHR) treatments and reduces their efficacy. In addition to fertility disorders, obesity increases significantly the risks of many complications of pregnancy, delivery and neonatal health. However, a modest loss of 5-10% of total body weight can restore ovulation and improve pregnancy rates.
OBJECTIVES: 1) To design and implement a multidisciplinary program for lifestyle management of obese women, or overweight women with PCOS, who seek fertility treatment in a secondary AHR center. 2) To evaluate lifestyle benefits of this program and assess its impact on fertility, pregnancy and neonatal outcomes, as compared to a randomly assigned control group and to similar women seen in tertiary AHR centers. 3) To assess cost per live birth, and other measures of cost-effectiveness, of this program compared to the control group and tertiary AHR centers. 4) To effectively transfer knowledge obtained through these activities to relevant stakeholders in the health care and public health sectors.
METHODS AND APPROACH: In order to design the program for lifestyle management of obesity in infertile women, we will gather a Committee composed of members of our interdisciplinary research team and relevant collaborators. Objectives 2 and 3 - In order to achieve these objectives, 128 obese women (BMI ≥ 30 kg/m²), or overweight women with PCOS (BMI ≥ 27 kg/m²), consulting at the CHUS fertility clinic will be randomized to our lifestyle program, and will suspend fertility treatments for six months, or to standard fertility treatments, which are directly initiated. The results obtained will also be compared to those of women with the same criteria who will consult in 3 tertiary AHR clinics not offering a similar lifestyle management program.
IMPACT: This project is very important as it will generate new knowledge about the implementation, impacts and costs of a new lifestyle management program in obese infertile women. Our project will obtain valuable data on implementability of such a program; on benefits with regard to lifestyle, fertility and maternal and foetal complications during pregnancy; as well as on reduction in cost per live birth and other cost-effectiveness ratio.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Female Infertility, Polycystic Ovary Syndrome, Obesity
Keywords
Body Weight, Female, Infertility, Female/therapy, Infertility, Female/physiopathology, Obesity/physiopathology, Polycystic ovary syndrome, Pregnancy, Pregnancy Outcome, Weight Loss
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
130 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lifestyle counseling
Arm Type
Experimental
Arm Title
control
Arm Type
No Intervention
Intervention Type
Behavioral
Intervention Name(s)
Interdisciplinary lifestyle intervention
Other Intervention Name(s)
Lifestyle program for obese infertile women
Intervention Description
Individual meetings with a dietitian and a kinesiologist at 0, 3, 6 weeks and then every 6 weeks for 18 months or until delivery. A reminder phone call/email will also take place once between each meeting.
The program also includes 12 group sessions discussing subjects about nutrition, psychology and demonstration of physical activity.
Primary Outcome Measure Information:
Title
Rates of live birth
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
Secondary Outcome Measure Information:
Title
Fertility outcomes
Time Frame
18 months
Title
Pregnancy outcomes
Time Frame
Participants who will become pregnant: up to the end of pregnancy, an expected average of 18 months of follow-up in the study
Title
Neonatal outcomes
Time Frame
Participants who will become pregnant: up to the end of pregnancy, an expected average of 18 months of follow-up in the study
Title
Clinical outcomes
Description
Evolution of anthropometric measures, change in lifestyle habits, physical fitness level and evolution of readiness for change.
Time Frame
18 months
Title
Cost per life birth, and other measures of cost-effectiveness
Description
All costs (interventions and complications) to achieve one life birth, including either all women with a life birth or all enrolled women (by intervention arm).
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
Title
Clinical outcomes in male partners
Description
Evolution of anthropometric measures and change in lifestyle habits in male partners.
Time Frame
18 months
Title
Clinical outcomes of female participants
Description
Evolution of anthropometric measures, changes in lifestyle habits (diet, exercise, alcohol, tobacco), physical fitness level, evolution of readiness for change, etc.
Time Frame
18 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Patrice Baillargeon, MD
Organizational Affiliation
Université de Sherbrooke
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre hospitalier universitaire de Sherbrooke
City
Sherbrooke
State/Province
Quebec
ZIP/Postal Code
J1H 5N4
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
26635965
Citation
Duval K, Langlois MF, Carranza-Mamane B, Pesant MH, Hivert MF, Poder TG, Lavoie HB, Ainmelk Y, St-Cyr Tribble D, Laredo S, Greenblatt E, Sagle M, Waddell G, Belisle S, Riverin D, Jean-Denis F, Belan M, Baillargeon JP. The Obesity-Fertility Protocol: a randomized controlled trial assessing clinical outcomes and costs of a transferable interdisciplinary lifestyle intervention, before and during pregnancy, in obese infertile women. BMC Obes. 2015 Dec 1;2:47. doi: 10.1186/s40608-015-0077-x. eCollection 2015.
Results Reference
derived
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Evaluation of Clinical Outcomes and Costs of a Lifestyle Intervention in Obese Infertile Women
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