Healthy Living in Pregnancy (GeLiS)
Primary Purpose
Lifestyle, Weight Gain, Pregnancy
Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Lifestyle intervention
Sponsored by
About this trial
This is an interventional prevention trial for Lifestyle
Eligibility Criteria
Inclusion Criteria:
- Gestational age ≤ 12th week of gestation
- Age: 18 years to 43 years
- Prepregnancy BMI ≥ 18.5 kg/m2 and ≤ 40.0 kg/m2
- Sufficient German language skills
- Written informed consent
Exclusion Criteria:
- Multiple pregnancy
- Any condition preventing physical activity such as placenta praevia, persistent bleeding, cervical incompetence
- Prepregnancy diabetes or early diagnosed gestational diabetes
- Uncontrolled chronic diseases (e.g. thyroid dysfunction)
- Psychiatric or psychosomatic diseases
- Any condition that may interfere with the study protocol
Sites / Locations
- AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
- AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
- AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
- AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
- AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention
No intervention
Arm Description
Lifestyle intervention
Standard prenatal care, short information leaflet about healthy lifestyle in pregnancy
Outcomes
Primary Outcome Measures
Gestational weight gain
Proportion of pregnant women showing excessive gestational weight gain according to Institute of Medicine (IOM) guidelines
Secondary Outcome Measures
Full Information
NCT ID
NCT01958307
First Posted
October 4, 2013
Last Updated
September 19, 2017
Sponsor
Technical University of Munich
1. Study Identification
Unique Protocol Identification Number
NCT01958307
Brief Title
Healthy Living in Pregnancy
Acronym
GeLiS
Official Title
Healthy Living in Pregnancy
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2013 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
September 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Technical University of Munich
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Multicenter and multidisciplinary public health project in 10 regions of Bavaria, a federal state of Germany, targeting maternal and fetal health. The objective of this trial is to evaluate the efficacy of a lifestyle intervention program focusing on diet, physical activity and weight monitoring during pregnancy. The intervention comprises 4 individual counseling sessions addressing healthy living. Primary outcome: gestational weight gain. Secondary outcomes are pregnancy and obstetric complications like gestational diabetes and rate of caesarean sections as well as offspring health.
The lifestyle intervention program is adapted to the German health care system to allow an immediate implementation after successful evaluation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lifestyle, Weight Gain, Pregnancy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2500 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Lifestyle intervention
Arm Title
No intervention
Arm Type
No Intervention
Arm Description
Standard prenatal care, short information leaflet about healthy lifestyle in pregnancy
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle intervention
Intervention Description
The intervention program consists of four individual counseling modules focusing on diet, physical activity and weight monitoring (12th-16th, 16th-20th, 30th-34th week of gestation and 6th-8th week postpartum). The counseling sessions are given by carefully trained midwives or medical staff in combination with prenatal visits and follow a standardized curriculum. Women are provided with brochures including a list of adequate prenatal exercise programs and a pedometer. Furthermore, they receive a chart personalized according to their baseline BMI category to monitor weight development.
Primary Outcome Measure Information:
Title
Gestational weight gain
Description
Proportion of pregnant women showing excessive gestational weight gain according to Institute of Medicine (IOM) guidelines
Time Frame
4 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
43 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Gestational age ≤ 12th week of gestation
Age: 18 years to 43 years
Prepregnancy BMI ≥ 18.5 kg/m2 and ≤ 40.0 kg/m2
Sufficient German language skills
Written informed consent
Exclusion Criteria:
Multiple pregnancy
Any condition preventing physical activity such as placenta praevia, persistent bleeding, cervical incompetence
Prepregnancy diabetes or early diagnosed gestational diabetes
Uncontrolled chronic diseases (e.g. thyroid dysfunction)
Psychiatric or psychosomatic diseases
Any condition that may interfere with the study protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hans Hauner, Prof.
Organizational Affiliation
Else Kröner-Fresenius-Zentrum für Ernährungsmedizin
Official's Role
Principal Investigator
Facility Information:
Facility Name
AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
City
Bayreuth
ZIP/Postal Code
95447
Country
Germany
Facility Name
AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
City
Fürstenfeldbruck
ZIP/Postal Code
82256
Country
Germany
Facility Name
AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
City
Fürth
ZIP/Postal Code
90763
Country
Germany
Facility Name
AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
City
Regensburg
ZIP/Postal Code
93057
Country
Germany
Facility Name
AELF, Fachzentrum L 3.10 Ernährung/Gemeinschaftsverpflegung
City
Würzburg
ZIP/Postal Code
97074
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
23865624
Citation
Rauh K, Gabriel E, Kerschbaum E, Schuster T, von Kries R, Amann-Gassner U, Hauner H. Safety and efficacy of a lifestyle intervention for pregnant women to prevent excessive maternal weight gain: a cluster-randomized controlled trial. BMC Pregnancy Childbirth. 2013 Jul 16;13:151. doi: 10.1186/1471-2393-13-151.
Results Reference
background
PubMed Identifier
22205307
Citation
Hauner H, Much D, Vollhardt C, Brunner S, Schmid D, Sedlmeier EM, Heimberg E, Schuster T, Zimmermann A, Schneider KT, Bader BL, Amann-Gassner U. Effect of reducing the n-6:n-3 long-chain PUFA ratio during pregnancy and lactation on infant adipose tissue growth within the first year of life: an open-label randomized controlled trial. Am J Clin Nutr. 2012 Feb;95(2):383-94. doi: 10.3945/ajcn.111.022590. Epub 2011 Dec 28.
Results Reference
background
PubMed Identifier
19295192
Citation
Hauner H, Vollhardt C, Schneider KT, Zimmermann A, Schuster T, Amann-Gassner U. The impact of nutritional fatty acids during pregnancy and lactation on early human adipose tissue development. Rationale and design of the INFAT study. Ann Nutr Metab. 2009;54(2):97-103. doi: 10.1159/000209267. Epub 2009 Mar 19.
Results Reference
background
PubMed Identifier
35313852
Citation
Raab R, Hoffmann J, Spies M, Geyer K, Meyer D, Gunther J, Hauner H. Are pre- and early pregnancy lifestyle factors associated with the risk of preterm birth? A secondary cohort analysis of the cluster-randomised GeliS trial. BMC Pregnancy Childbirth. 2022 Mar 21;22(1):230. doi: 10.1186/s12884-022-04513-5.
Results Reference
derived
PubMed Identifier
32703266
Citation
Johar H, Hoffmann J, Gunther J, Atasoy S, Stecher L, Spies M, Hauner H, Ladwig KH. Evaluation of antenatal risk factors for postpartum depression: a secondary cohort analysis of the cluster-randomised GeliS trial. BMC Med. 2020 Jul 24;18(1):227. doi: 10.1186/s12916-020-01679-7.
Results Reference
derived
PubMed Identifier
31711430
Citation
Hoffmann J, Gunther J, Geyer K, Stecher L, Rauh K, Kunath J, Meyer D, Sitzberger C, Spies M, Rosenfeld E, Kick L, Oberhoffer R, Hauner H. Effects of a lifestyle intervention in routine care on prenatal physical activity - findings from the cluster-randomised GeliS trial. BMC Pregnancy Childbirth. 2019 Nov 11;19(1):414. doi: 10.1186/s12884-019-2553-7. Erratum In: BMC Med Educ. 2019 Dec 24;19(1):470.
Results Reference
derived
PubMed Identifier
30636636
Citation
Kunath J, Gunther J, Rauh K, Hoffmann J, Stecher L, Rosenfeld E, Kick L, Ulm K, Hauner H. Effects of a lifestyle intervention during pregnancy to prevent excessive gestational weight gain in routine care - the cluster-randomised GeliS trial. BMC Med. 2019 Jan 14;17(1):5. doi: 10.1186/s12916-018-1235-z.
Results Reference
derived
PubMed Identifier
24678761
Citation
Rauh K, Kunath J, Rosenfeld E, Kick L, Ulm K, Hauner H. Healthy living in pregnancy: a cluster-randomized controlled trial to prevent excessive gestational weight gain - rationale and design of the GeliS study. BMC Pregnancy Childbirth. 2014 Mar 28;14:119. doi: 10.1186/1471-2393-14-119.
Results Reference
derived
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Healthy Living in Pregnancy
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