[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"preconception-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:preconception-care":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":33,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":5},"100381090","healthy-for-my-baby--rct-of-a-lifestyle-intervention-for-overweight-women-in-preconception-100381090",false,"NCT04242069","Healthy for my Baby- RCT of a Lifestyle Intervention for Overweight Women in Preconception","Healthy for my Baby- A Randomized Controlled Trial Assessing a Preconception Clinically Integrated Technological Intervention to Improve the Lifestyle of Overweight Women and Their Partners","Inclusion Criteria:\n\n* Women and their partner who wish to conceive within 12 months of trial inclusion\n* Woman's body mass index ≥ 25 kg\u002Fm2\n* Access to a smart phone\n\nExclusion Criteria:\n\n* Insufficient knowledge of French or English\n* Anticipated move to another region\n* Personal history of infertility\n* Type 1 or 2 diabetes mellitus\n* Prior bariatric surgery\n* Active eating disorder established by clinical diagnosis\n* Medical contraindication to pregnancy\n* Medical contraindication to physical activity\n* Participation in another intensive lifestyle intervention\n* Known or anticipated disease or surgery likely to cause an important weight loss\n* Multiple pregnancies will be excluded from the pregnancy follow-up to limit aberrant data",true,"ALL","18 Years","40 Years",{"count":21,"type":22},68,"ESTIMATED","INTERVENTIONAL",[25],"NA","The purpose of this study is to determine whether an intervention combining motivational interviewing and follow-up with a mobile phone application will help overweight women and their partners adopt healthy lifestyle habits in the preconception period. This study will also evaluate the impact of the intervention on the weight, waist circumference, and body fat of women and their partners. Women and their partners will be followed through pregnancy to explore the effects of the intervention on the adequacy of gestational weight gain, rates of pregnancy complications, delivery mode, and infant birth weight.",[28,29,30,31,32],"Overweight and Obesity","Pregnancy Complications","Health Behavior","Life Style","Preconception Care",[34],"Metabolomics","RECRUITING","2025-03-28",{"date":38,"type":39},"2025-04-02","ACTUAL",{"date":41,"type":39},"2021-06-18",{"date":43,"type":22},"2026-07-30",{"name":45,"class":46},"Université de Sherbrooke","OTHER",{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":16,"sex":53,"minAge":4,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":73},"100506168","generation-r-next---optimaal-opgroeien-100506168","NCT05870878","Generation R Next - Optimaal Opgroeien","Inclusion Criteria:\n\nWomen and their parents:\n\n* Planning a pregnancy or early pregnancy up to \\\u003C 12 weeks\n* With the presence of at least one of the predetermined risk factors\n* Residential address in the municipality of Rotterdam and expected residential address in the municipality of Rotterdam at the birth of their child\n* Consent for participation\n\nExclusion Criteria:\n\nWomen and their partners:\n\n* Temporary or complete withdrawal from participation\n* Gestational age \\> 12+0 at study entry","FEMALE",{"count":55,"type":22},1750,[25],"The aim of this randomized controlled trial is to improve birth outcomes and long-term outcomes in mother and child by optimizing lifestyle,nutrition and stress experience in the preconception period and early pregnancy in women and men\n\nThe main research question that will be addressed is: Does an intervention focused on optimizing preconception and early pregnancy lifestyle, nutrition and stress improve the birth outcomes and long-term outcomes in mother and child?\n\nParticipants will receive an individual lifestyle consultation at the start of the study. Depending on their study arm, participants will receive an additional lifestyle program focused on health during preconception and early pregnancy, coping with stress and adherence to a healthy(er) lifestyle. The given advices are based on national guidelines.\n\nResearchers will compare the intervention group and control group to see if (adherence to) this lifestyle program improve birth outcomes and long-term outcomes in mother and child.",[59,60,61,32,62,29,63],"Pregnancy Early","Outcome, Adverse Birth","Lifestyle Factors","Pregnancy Outcome","Risk Reduction Behavior","2024-08-30",{"date":66,"type":39},"2024-09-04",{"date":68,"type":39},"2023-01-19",{"date":70,"type":22},"2030-11-08",{"name":72,"class":46},"Erasmus Medical Center",1]