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Trials / Completed

CompletedNCT01566929

Weight Management Intervention for Obese Women and the Live Birth Outcome of in Vitro Fertilization (IVF)

Weight Management Interventions for Obese Women and the Live Birth Outcome of in Vitro Fertilization (IVF): a Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
317 (actual)
Sponsor
Sahlgrenska University Hospital · Academic / Other
Sex
Female
Age
18 Years – 37 Years
Healthy volunteers
Not accepted

Summary

The primary aim of the study is to evaluate if weight management intervention for obese women (BMI≥30\<35 kg/m2) prior to IVF improves the outcome assessed as live birth per participating woman, as compared to women where no intervention was made.

Detailed description

1. There will be two groups of patients. 1. The first group (n=167) will receive weight management intervention during up to four months prior to IVF treatment.The group randomized to intervention will start an intensive weight reduction plan. The aim of the weight reduction is to reach as close to normal BMI (\<25.0 kg/m2) as possible during a time of approximately 4 months. The purpose of the dietary intervention is to create a negative energy balance to induce weight loss. The intervention starts with 12 weeks of a low calorie liquid formula diet (LCD) and thereafter, diet re-introduction and weight control stabilization until IVF treatment begins. Should the patient for some reason be unable to fulfil the LCD-treatment, she will anyhow have an individualized dietary counselling to help her loose weight until the time for her IVF-treatment. 2. The second group (n=167) will start their IVF-treatment directly without other intervention than written advice about the benefits of weight reduction and exercise. The group randomized directly to IVF-treatment will start the treatment as soon as possible after randomization, preferably within that menstrual cycle. 2. Tertiary aim is a follow-up 2 years after randomization to the study with questionnaires to the couple in both the intervention and the control groups. A special questionnaire will cover the weights of the couple and if the woman has had any pregnancies or live births after concluding the study. For the women having achieved a live birth in the index-cycle of IVF the number of children and also follow-up of the children will be performed by assessing medical records from pediatric clinic (if applicable) and child health care centres covering birth data, general health and weight of the children at birth and at the assessment date. Eating -habits and -patterns and quality of life parameters will be assessed with the same three questionnaires that were filled in after randomization.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLow calorie diet treatmentReduction of calorie intake to only 800 kcal/day by using LCD during 12 weeks

Timeline

Start date
2010-10-01
Primary completion
2016-01-01
Completion
2018-04-01
First posted
2012-03-30
Last updated
2018-09-07

Locations

9 sites across 3 countries: Denmark, Iceland, Sweden

Source: ClinicalTrials.gov record NCT01566929. Inclusion in this directory is not an endorsement.