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Effect of Weight Loss and Lactation (the EVA-trial) (EVA)

Primary Purpose

Cardiovascular Risk Factor

Status
Active
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Breastfeeding promotion intervention
Diet and weight loss intervention
Sponsored by
University of Oslo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Risk Factor

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women in gestational week <32, with a pre-pregnant BMI 25-35 kg/m2
  • Residence in Oslo/Bærum and surrounding area
  • Intention to breastfeed their child
  • Able to read and write in Norwegian.

Exclusion Criteria:

  • Medication that influences lipid or glucose metabolism
  • Chronic disease that influences lipid or glucose metabolism (e.g. diabetes (World Health Organization, WHO, 2006) or diabetes in pregnancy (WHO 2013))
  • Premature birth (before week 36)
  • Preeclampsia
  • Previous breast reducing surgery

Sites / Locations

  • University of Oslo

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

No Intervention

Arm Label

Breastfeeding promotion intervention (BPI)

Diet- and weight loss intervention (D)

BPI and D

Control

Arm Description

Both interventions.

Outcomes

Primary Outcome Measures

Changes in body weight (kg) between visits.
Measured in light clothing without shoes. Together with measured height (m) will be used to calculate Body Mass Index.
Changes in markers of lipid- and glucose metabolism between visits.
Measured in mmol/l: total cholesterol, low-density lipoprotein, high-density lipoprotein, triglycerides and glucose In percentage: HbA1c In pmol/l: insulin.

Secondary Outcome Measures

Changes in lipid subclasses (mmol/l), lipoprotein size (nm) and apolipoproteins between visits
In g/l: apolipoprotein (apo) B and apo A1. In mmol/l: lipoprotein (a)
Changes in blood pressure, diastolic and systolic between visits
Measured after 5 min rest, mean of last 2 of 3 measurements (mmHg)
Changes in waist and hip (cm) circumference between visits
A measuring tape specifically designed for waist circumference (Seca) will be used according to a standardized procedure Measurements will be taken against the skin at the approximate midpoint between the lower margin of the last palpable rib and the top of the iliac crest. Hip is measured over the widest point on the buttocks.
Changes in body composition (fat free mass in kg and fat mass in kg) between visits.
Measured by Bioelectrical impedance and Dual X-ray Absorptiometry

Full Information

First Posted
April 30, 2018
Last Updated
May 9, 2023
Sponsor
University of Oslo
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1. Study Identification

Unique Protocol Identification Number
NCT03580057
Brief Title
Effect of Weight Loss and Lactation (the EVA-trial)
Acronym
EVA
Official Title
Effect of Weight Loss and Lactation on Cardiovascular Risk Factors (the EVA-trial)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 30, 2018 (Actual)
Primary Completion Date
December 15, 2023 (Anticipated)
Study Completion Date
December 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Oslo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A randomized controlled trial aiming to investigate the effects and possible interactions of diet induced weight loss and lactation on cardiometabolic profile

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Risk Factor

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
156 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Breastfeeding promotion intervention (BPI)
Arm Type
Experimental
Arm Title
Diet- and weight loss intervention (D)
Arm Type
Experimental
Arm Title
BPI and D
Arm Type
Experimental
Arm Description
Both interventions.
Arm Title
Control
Arm Type
No Intervention
Intervention Type
Behavioral
Intervention Name(s)
Breastfeeding promotion intervention
Intervention Description
Promotion (education, support and supervision) of breastfeeding by experienced breastfeeding consultants and midwife, in order to follow the Norwegian guideline of 6 months exclusive breastfeeding and partial breastfeeding for a year.
Intervention Type
Behavioral
Intervention Name(s)
Diet and weight loss intervention
Intervention Description
12-week program of dietary behavior modification treatment (LEVA-method by Bertz et al. Am J Clin Nutr 2012;96:698), leading to 6 kg weight loss (0.5 kg per week) and a healthier diet (less sugar, snacks, full fat products, more vegetables and fruit, smaller portion sizes). Weight is monitored by phone contact every second week. After 12 weeks, the women are followed up by e-mail contact for 9 additional months.
Primary Outcome Measure Information:
Title
Changes in body weight (kg) between visits.
Description
Measured in light clothing without shoes. Together with measured height (m) will be used to calculate Body Mass Index.
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in markers of lipid- and glucose metabolism between visits.
Description
Measured in mmol/l: total cholesterol, low-density lipoprotein, high-density lipoprotein, triglycerides and glucose In percentage: HbA1c In pmol/l: insulin.
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Secondary Outcome Measure Information:
Title
Changes in lipid subclasses (mmol/l), lipoprotein size (nm) and apolipoproteins between visits
Description
In g/l: apolipoprotein (apo) B and apo A1. In mmol/l: lipoprotein (a)
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in blood pressure, diastolic and systolic between visits
Description
Measured after 5 min rest, mean of last 2 of 3 measurements (mmHg)
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (15 months postpartum)
Title
Changes in waist and hip (cm) circumference between visits
Description
A measuring tape specifically designed for waist circumference (Seca) will be used according to a standardized procedure Measurements will be taken against the skin at the approximate midpoint between the lower margin of the last palpable rib and the top of the iliac crest. Hip is measured over the widest point on the buttocks.
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in body composition (fat free mass in kg and fat mass in kg) between visits.
Description
Measured by Bioelectrical impedance and Dual X-ray Absorptiometry
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Other Pre-specified Outcome Measures:
Title
Changes in circulating inflammation markers such as cytokines, high sensitivity C-Reactive Protein (hsCRP), CRP and microCRP between visits.
Description
Measured in mg/l
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in environmental toxins in breast milk and blood, such as dioxines and Persistent Organic Pollutants (POPs) between visits.
Description
Presented on lipid weight basis (ng/g)
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in plasma metabolomics such as lactate, pyruvate, citrate and amino acids between visits.
Description
Measured in mmol/l
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in PBMC (peripheral blood mononuclear cell) gene expression levels of markers of inflammation and lipid metabolism between visits.
Description
Changes in levels of markers of inflammation and lipid metabolism at PBMC gene expression level.
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in hemostatic markers such as plasminogen activator inhibitor-1 (PAI-1) antigen and von Willebrand factor (vWF) between visits.
Description
PAI-1 measured in ng/mL, vWF measured in IU/dl
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in hormones such as prolactin, estradiol, progesterone between visits.
Description
Measured in nmol/l
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in markers of micronutrient status such as Hb, ferritin and vitamin D between visits.
Description
Ferritin will be evaluated in relation to CRP.
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in dietary intake (kcal) and nutrient composition measured by 4-day weighed diet record between 3 visits
Description
Nutrient composition calculation in nutrient composition software Dietist Net Pro
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in physical activity (METs, activity counts, step counts) between visits.
Description
measured by ActiGraph (GT3X)
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in quality of life (QOL) measured by RAND 36-Item Short-Form Health Survey Instrument (SF-36) between visits.
Description
The SF-36 RAND consists of 36 questions grouped into 8 dimensions: physical functioning, limitations in physical role functioning, bodily pain, general health, vitality, social functioning, limitations in emotional role functioning, and mental health. Each dimension is scored from 0 (worst imaginable health) to 100 (best imaginable health).
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in quality of life (QOL) measured by EuroQol 5D (EQ-5D-5L) between visits.
Description
EQ-5D-5L measures 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression (self-classified). Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems, and extreme problems. The respondent is asked to indicate his/her health state by ticking (or placing a cross) in the box against the most appropriate statement in each of the 5 dimensions (levels of perceived problems from 1. level indicating no problem to 5. level indicating extreme problems). This decision results in a 1-digit number expressing the level selected for that dimension. The digits for 5 dimensions can be combined in a 5-digit number describing the respondent's health state. EQ-5D-5L health states may be converted into a single index value.The index values, presented in country specific value sets, facilitates the calculation of quality-adjusted life years (QALYs) that will be used to inform economic evaluations of the interventions.
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)
Title
Changes in quality of life (QOL) measured by EuroQol Visual Analog Scale (EQ-VAS) between visits.
Description
The EQ-VAS records the respondent's self-rated health on a 20-cm visual analogue scale . The scale is numbered from 0 (the worst health you can imagine) to 100 (the best health you can imagine.) This information can be used as a quantitative measure of health.
Time Frame
Visit 1 (2 weeks postpartum, visit 2 (6 months postpartum) and visit 3 (post weaning ~15 months postpartum)

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Only pregnant women are eligible
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women in gestational week <32, with a pre-pregnant BMI 25-35 kg/m2 Residence in Oslo/Bærum and surrounding area Intention to breastfeed their child Able to read and write in Norwegian. Exclusion Criteria: Medication that influences lipid or glucose metabolism Chronic disease that influences lipid or glucose metabolism (e.g. diabetes (World Health Organization, WHO, 2006) or diabetes in pregnancy (WHO 2013)) Premature birth (before week 36) Preeclampsia Previous breast reducing surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hilde K Brekke, PhD
Organizational Affiliation
University of Oslo
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Oslo
City
Oslo
ZIP/Postal Code
0317
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Effect of Weight Loss and Lactation (the EVA-trial)

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