A Lifestyle Intervention to Improve in Vitro Fertilization Results (W+D)
Primary Purpose
Sterility, Placenta; Implantation, Risk Reduction Behavior
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Daily walking
Dietary recommendations
Sponsored by
About this trial
This is an interventional prevention trial for Sterility
Eligibility Criteria
Inclusion Criteria:
- women undergoing assisted reproduction
Exclusion Criteria:
- liver failure, kidney failure or other conditions that prevent the patient from eating proteins.
- multiple pregnancy.
- paraplegia, hemiplegia, arthropathy and other conditions that prevent the participant from exercising.
- participants lost to follow-up.
- conditions that may strongly affect pregnancy results, such as a serious accident
- participants assigned to non-intervention group following the recommendations given to intervention group.
Sites / Locations
- Hospital Federal dos Servidores do Estado, Ministry of Health
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Standard follow-up (controls)
W+D protocol (lifestyle intervention)
Arm Description
Given that depressive disorders may increase the risk of spontaneous abortions, antidepressants will be not discontinued. However, expectant mothers on paroxetine or sertraline, which have been reported to increase the incidence of cardiac malformations, will be switched to fluoxetine.
Daily walking and dietary recommendations. Expectant mothers on paroxetine or sertraline will be switched to fluoxetine
Outcomes
Primary Outcome Measures
The rate of viable pregnancies
Secondary Outcome Measures
The rate of fist trimester losses
The rate of second and third trimester losses
The rate of preeclampsia, eclampsia and HELLP syndrome
Cramps or bleeding during the first trimester requiring progesterone
The rate of prematurity
The rate of intrauterine growth restriction
Maternal weight gain
The rate of gestational diabetes
The rate of neonatal hypoglycemia
The rate of neonatal hyperbilirubinemia requiring phototherapy
Full Information
NCT ID
NCT02648555
First Posted
January 4, 2016
Last Updated
January 6, 2016
Sponsor
Hospital dos Servidores do Estado do Rio de Janeiro
Collaborators
Gaffree & Guinle Universitary Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02648555
Brief Title
A Lifestyle Intervention to Improve in Vitro Fertilization Results
Acronym
W+D
Official Title
A Lifestyle Intervention to Improve in Vitro Fertilization Results
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Unknown status
Study Start Date
May 2016 (undefined)
Primary Completion Date
May 2018 (Anticipated)
Study Completion Date
May 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital dos Servidores do Estado do Rio de Janeiro
Collaborators
Gaffree & Guinle Universitary Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Embryo adhesion and placentation depend on tissue plasminogen activator (tPA)-mediated activation of brain-derived neurotrophic factor, vascular endothelial growth factor and other growth factors, formation of hemidesmosomes, and degradation of extracellular matrix and basement membrane, either directly or by activating matrix metalloproteinases.
Since glucose and insulin stimulate release of a major tPA inhibitor by endothelial cells - plasminogen activator inhibitor (PAI)-1 - the investigators hypothesized that lifestyle interventions proven effective in maintaining glucose and insulin levels within the normal range would increase the take home baby rate in women undergoing assisted reproduction.
Detailed Description
Tissue plasminogen activator (tPA) has a well-known role in the coagulation pathway. tPA converts plasminogen to plasmin. Plasmin dissolves fibrin clots, thus limiting thrombus formation to the site of vascular injury.
In the extravascular compartment, tPA is a pivotal mediator of tissue formation and remodeling. Due to its proteolytic activity, tPA participates in processes as diverse as embryo adhesion, placental angiogenesis and vasculogenesis, and neuronal plasticity. Embryo adhesion and placentation, for example, depend on tPA-mediated activation of brain-derived neurotrophic factor, vascular endothelial growth factor and other growth factors, formation of hemidesmosomes, and degradation of extracellular matrix and basement membrane, either directly or by activating matrix metalloproteinases.
Assuming low tPA activity would impair both blood clot dissolution and placentation, the investigators postulated that patients with consecutive first-trimester abortions would have a high prevalence of severe dysmenorrhea, accompanied by the passage of large clots.
In 2011, the investigators assessed the prevalence of severe dysmenorrhea during early adolescence in two groups. The first one was made of women with ≥ 2 consecutive first-trimester abortions, and the other, of women with ≥ 2 living births, and no losses or preterm deliveries. Severe dysmenorrhea was defined as suprapubic menstrual cramp, intense enough to cause repeated absenteeism from school or fainting in the absence of analgesia. Early adolescents are unlikely to use contraceptives, or to have become pregnant, two situations that may reduce the pain. In this study, severe dysmenorrhea increased the chances of having consecutive first-trimester miscarriages by sevenfold (95% Confidence Interval: 3.4 to 14.1; p<0.001).
Since glucose and insulin stimulate release of a major tPA inhibitor by endothelial cells - plasminogen activator inhibitor (PAI)-1 - the investigators hypothesized that lifestyle interventions proven effective in maintaining glucose and insulin levels within the normal range would increase the take home baby rate in women undergoing assisted reproduction.
The protocol has already been tested at a Brazilian tertiary care center in women with unexplained consecutive first-trimester abortions, conceiving spontaneously. The objective of this study was to observe the impact of lifestyle interventions on the take home baby rate, and to observe if the intervention could reduce the prevalence of preeclampsia and neonatal hypoglycemia.
From 2011 to 2015, 480 patients aged 18 to 42 years with ≥ 2 consecutive first-trimester abortions documented by pathology or ultrasonography, were randomly assigned to protocol Walking and Diet (W+D) or to standard follow-up (controls). Women were enrolled independent of having had severe dysmenorrhea during adolescence. Patients assigned to protocol W+D were instructed to walk briskly for ≥ 40 minutes seven days a week. In addition, they were recommended to avoid high-carbohydrate meals such as snacks, candies, fiber-free juices, coconut water and sugar-sweetened beverages, and to eat two daily servings of meat, poultry, fish (e.g. 2 g/kg) or other protein-rich food, starting when they decided to get pregnant and continuing until delivery. Women with antiphospholipid antibodies, second- or third-trimester losses, multiple pregnancies, anatomical abnormalities that could increase the risk of first-trimester abortions, or any condition requiring a priori anticoagulation were excluded.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sterility, Placenta; Implantation, Risk Reduction Behavior, Lifestyle, Neonatal Hypoglycemia
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
240 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard follow-up (controls)
Arm Type
No Intervention
Arm Description
Given that depressive disorders may increase the risk of spontaneous abortions, antidepressants will be not discontinued. However, expectant mothers on paroxetine or sertraline, which have been reported to increase the incidence of cardiac malformations, will be switched to fluoxetine.
Arm Title
W+D protocol (lifestyle intervention)
Arm Type
Experimental
Arm Description
Daily walking and dietary recommendations. Expectant mothers on paroxetine or sertraline will be switched to fluoxetine
Intervention Type
Behavioral
Intervention Name(s)
Daily walking
Intervention Description
Participants will be instructed to walk briskly for >40 minutes, 7 days a week.
Intervention Type
Behavioral
Intervention Name(s)
Dietary recommendations
Intervention Description
Participants will be instructed to eat at least two daily servings of meat, poultry, fish (e.g. 2 g/kg) or other protein-rich food, starting at least one week before embryo transfer and continuing until delivery. They will be also recommended to avoid high-glycemic index meals (high-carbohydrate, low-fiber), such as snacks, candies, fiber-free juices, coconut water, and sugar-sweetened beverages, particularly carbonated soft drinks and sport drinks.
Patients suffering from nausea usually do not tolerate solid food. As a result, fiber-free juices and sugar-sweetened beverages account of most of their caloric intake, which may cause non-adherence to the protocol. Women with nausea or vomiting will be treated with ondansetron.
Primary Outcome Measure Information:
Title
The rate of viable pregnancies
Time Frame
two years
Secondary Outcome Measure Information:
Title
The rate of fist trimester losses
Time Frame
four years
Title
The rate of second and third trimester losses
Time Frame
four years
Title
The rate of preeclampsia, eclampsia and HELLP syndrome
Time Frame
four years
Title
Cramps or bleeding during the first trimester requiring progesterone
Time Frame
four years
Title
The rate of prematurity
Time Frame
four years
Title
The rate of intrauterine growth restriction
Time Frame
four years
Title
Maternal weight gain
Time Frame
four years
Title
The rate of gestational diabetes
Time Frame
four years
Title
The rate of neonatal hypoglycemia
Time Frame
four years
Title
The rate of neonatal hyperbilirubinemia requiring phototherapy
Time Frame
four years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
women undergoing assisted reproduction
Exclusion Criteria:
liver failure, kidney failure or other conditions that prevent the patient from eating proteins.
multiple pregnancy.
paraplegia, hemiplegia, arthropathy and other conditions that prevent the participant from exercising.
participants lost to follow-up.
conditions that may strongly affect pregnancy results, such as a serious accident
participants assigned to non-intervention group following the recommendations given to intervention group.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Silvia Hoirisch-Clapauch, MD, PhD
Phone
+55-21-999737500
Email
sclapauch@ig.com.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Silvia Hoirisch-Clapauch, MD, PhD
Organizational Affiliation
Hospital Federal dos Servidores do Estado, Ministry of Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Federal dos Servidores do Estado, Ministry of Health
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
20221-903
Country
Brazil
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Silvia Hoirisch-Clapauch, MD, PhD
Phone
+55-21-99973-7500
Email
sclapauch@ig.com.br
First Name & Middle Initial & Last Name & Degree
Silvia Hoirisch-Clapauch, MD
12. IPD Sharing Statement
Learn more about this trial
A Lifestyle Intervention to Improve in Vitro Fertilization Results
We'll reach out to this number within 24 hrs