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An Optimized Programming of Healthy Children (APPROACH)

Primary Purpose

Pregnancy, Obesity, Gestational Age and Weight Conditions

Status
Active
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
High-Protein/Low-GI Diet
Low-protein/High-GI Diet
Sponsored by
University of Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pregnancy focused on measuring Gestational weight gain, Obese women, Fetal programming, Metabolic disorders, Development of obesity, Development og overweight, Complications during pregnancy and birth

Eligibility Criteria

18 Years - 42 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Birth planed at Copenhagen University Hospital Herlev
  • Pre-pregnancy BMI 28-45
  • Age 18-42 years
  • Speak and understand oral and written Danish
  • Singleton pregnancy

Exclusion Criteria:

  • Multiple pregnancy
  • History of spontaneous abortions or gestational diabetes or preeclampsia or spontaneous preterm birth
  • Dairy product intolerant or allergic
  • > 10 kg weight change during the past year
  • Abuse of alcohol or drugs (>14 units of alcohol per week)
  • Critical or chronic disease: diabetes, kidney disease, medically treated heart diseases or arthritis, sarcoidosis, tuberculosis, cancer, liver disease, inflammatory gastrointestinal or lung disease, known active metabolic disease.

Sites / Locations

  • University of Copenhagen, Faculty of Sceience, NEXS

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

High-protein/Low-GI Diet

Low-protein/High-GI Diet

Arm Description

High-protein (25-28 E%), especially marine- and dairy-protein (8-10 E%) and low-GI (GI<55) ad libitum Diet in accordance with the principles of palatability and sustainability of the New Nordic Diet.

Ad libitum diet based on the Danish National Guidelines (NNR) (protein 10-20 E%; no information on restricting glycaemic load (GI ~ 60)) and in accordance with the principles of palatability and sustainability of the New Nordic Diet.

Outcomes

Primary Outcome Measures

Gestational weight gain
Changes in bodyweight, body composition (Magnetic Resonance Imaging) and measurements of body fat by means of skinfold thickness and mid-upper arm circumference.

Secondary Outcome Measures

Growth and development of fetus and child
Fetus: Nuchal Translucency Scan (once gw 11+3 - 14+0) and ultrasound scan (gw 28, 32, 36); child: Height, weight, body composition (Bioimpedance (month 6,18)and Dual-energy X-ray absorptiometry, DXA (month 0, 36, year 5, 9)), skin fold thickness and mid-upper arm circumference, IGF-1.
Fetal programming of obesity and metabolic disorders
Fasting blod samples (month 0 from umbilical cord), not at 6 months; dietary intake, physical activity, growth and development

Full Information

First Posted
July 3, 2013
Last Updated
September 29, 2021
Sponsor
University of Copenhagen
Collaborators
The Danish Dairy Research Foundation, Denmark, Nordea-Fonden, Denmark, LEGO Charity, Denmark, Pharma Nord, Danish Agriculture and Food Council, Svineafgiftsfonden
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1. Study Identification

Unique Protocol Identification Number
NCT01894139
Brief Title
An Optimized Programming of Healthy Children (APPROACH)
Official Title
An Optimized Programming of Healthy Children (APPROACH) - The Most Favourable Dietary Protein:Carbohydrate Ratio During Pregnancy in the Context of New Nordic Diet
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 4, 2014 (Actual)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
December 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Copenhagen
Collaborators
The Danish Dairy Research Foundation, Denmark, Nordea-Fonden, Denmark, LEGO Charity, Denmark, Pharma Nord, Danish Agriculture and Food Council, Svineafgiftsfonden

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Nutrition Research Unit at Copenhagen University Hospital Herlev will during the fall 2013 initiate a randomized and controlled intervention study engaging 390 obese pregnant women. The overall aim of APPROACH is to investigate how an optimal diet during pregnancy influences the programming of the offspring. The children will after birth be included in a prospective cohort according to maternal randomization and examined six times from delivery until the age of nine years.
Detailed Description
Overweight and excessive gestational weight gain (GWG) is associated with increased risk of high birth weight; furthermore there is increased risk of the child developing overweight, diabetes and other metabolic diseases in childhood or adulthood. The effect of reducing gestational weight gain while supplying optimized amount and sources of nutrients is not well investigated. Increased knowledge to the possibility and efficacy of preventing overweight and related diseases is necessary. Modification of protein source and increase in ratio of protein in relation to amount of carbohydrate and reduction of glycaemic index (GI) has in observational studies individually been linked to improved fetal body composition, metabolism and weight control later in life, and less weight gain and weight retention for the mother. The overall aim of APPROACH is to investigate how an optimal diet during pregnancy influences the programming of the offspring. This study will increase the knowledge of the effect of a specific nutrient composition and weight retention during pregnancy on growth and development during the foetal stage and until nine years off age, risk markers later metabolic diseases, especially diabetes and metabolic syndrome. APPROACH will be a dietary intervention investigating differences in responds to a high-protein, especially marine and dairy protein and low-GI diet versus a diet according to the Nordic Nutritional Recommendations. All visits and assessment will be performed by trained staff at Copenhagen University Hospital Herlev. Subjects will be women with expected delivery at Department of Gynaecology and Obstetrics and all examinations of gestational development and foetal growth will take place her; assessment of the children will be performed at the Department of Paediatrics. A total of 390 obese (body mass index (BMI) ≥ 30 kg/m2) pregnant women will be randomized to intervention or control and engage in the program from late first trimester or early second trimester to birth. After birth the children will be included in a prospective cohort according to maternal randomization and examined six times from delivery until the age of nine years. APPROACH will increase the knowledge of the effect of a nutrient composition with high protein for carbohydrate ratio and weight retention during pregnancy on growth and development during the foetal stage and until nine years off age, risk markers later metabolic diseases, especially diabetes and metabolic syndrome. Plasma lipids, markers of metabolic diseases, epigenetics and vitamin D status will be assessed at baseline and several times during pregnancy; and in both intervention and control group these data will increase the knowledge of the effect of supplementing with marine oils and vitamin D in pregnant women. Results from the intervention will be communicated to the general population and published in peer-relieved journals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy, Obesity, Gestational Age and Weight Conditions, Maternal Care for Excessive Fetal Growth, Metabolic Disorders
Keywords
Gestational weight gain, Obese women, Fetal programming, Metabolic disorders, Development of obesity, Development og overweight, Complications during pregnancy and birth

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
280 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High-protein/Low-GI Diet
Arm Type
Experimental
Arm Description
High-protein (25-28 E%), especially marine- and dairy-protein (8-10 E%) and low-GI (GI<55) ad libitum Diet in accordance with the principles of palatability and sustainability of the New Nordic Diet.
Arm Title
Low-protein/High-GI Diet
Arm Type
Active Comparator
Arm Description
Ad libitum diet based on the Danish National Guidelines (NNR) (protein 10-20 E%; no information on restricting glycaemic load (GI ~ 60)) and in accordance with the principles of palatability and sustainability of the New Nordic Diet.
Intervention Type
Other
Intervention Name(s)
High-Protein/Low-GI Diet
Intervention Type
Other
Intervention Name(s)
Low-protein/High-GI Diet
Primary Outcome Measure Information:
Title
Gestational weight gain
Description
Changes in bodyweight, body composition (Magnetic Resonance Imaging) and measurements of body fat by means of skinfold thickness and mid-upper arm circumference.
Time Frame
Gestational week 14, 15, 17, 21, 25, 28, 36, 39
Secondary Outcome Measure Information:
Title
Growth and development of fetus and child
Description
Fetus: Nuchal Translucency Scan (once gw 11+3 - 14+0) and ultrasound scan (gw 28, 32, 36); child: Height, weight, body composition (Bioimpedance (month 6,18)and Dual-energy X-ray absorptiometry, DXA (month 0, 36, year 5, 9)), skin fold thickness and mid-upper arm circumference, IGF-1.
Time Frame
Gestational week 11+2, 14+0, 28, 32, 36 and month 0, 6, 18, 36 and year 5, 9
Title
Fetal programming of obesity and metabolic disorders
Description
Fasting blod samples (month 0 from umbilical cord), not at 6 months; dietary intake, physical activity, growth and development
Time Frame
Month 0, 6,18, 36 and year 5, 9

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Birth planed at Copenhagen University Hospital Herlev Pre-pregnancy BMI 28-45 Age 18-42 years Speak and understand oral and written Danish Singleton pregnancy Exclusion Criteria: Multiple pregnancy History of spontaneous abortions or gestational diabetes or preeclampsia or spontaneous preterm birth Dairy product intolerant or allergic > 10 kg weight change during the past year Abuse of alcohol or drugs (>14 units of alcohol per week) Critical or chronic disease: diabetes, kidney disease, medically treated heart diseases or arthritis, sarcoidosis, tuberculosis, cancer, liver disease, inflammatory gastrointestinal or lung disease, known active metabolic disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arne V Astrup, Professor
Organizational Affiliation
Department of Nutrition, Exercise and sports, University of Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Copenhagen, Faculty of Sceience, NEXS
City
Copenhagen
State/Province
Frederiksberg
ZIP/Postal Code
1958
Country
Denmark

12. IPD Sharing Statement

Links:
URL
https://nexs.ku.dk
Description
Homepage of Department of Nutrition, Exercise and Sports, University of Copenhagen

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An Optimized Programming of Healthy Children (APPROACH)

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