跳至主要内容
临床试验/NCT04731688
NCT04731688已完成不适用

A Weight Maintenance Program Promoting Fat Loss in Pregnancy in Women With Obesity

Pennington Biomedical Research Center3 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年3月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
3
主要终点
Body weight

研究概览

简要总结

The aims of this randomized controlled trial are to determine the effects of a lifestyle program that supports weight maintenance and fat mass loss during pregnancy in women with obesity on changes in 1) maternal weight, fat mass, and cardiometabolic risk factors; 2) safety measures, including fetal and neonatal growth; 3) the mediators and moderators of the fat mass loss intervention and 4) the effects gestational fat mass loss has on reducing incidence of adverse obstetrical outcomes, including non-elective cesarean delivery, gestational diabetes, hypertension, and pre-eclampsia.

详细描述

One hundred pregnant women with obesity who are otherwise healthy will be studied from early pregnancy until approximately 2 weeks postpartum. Major assessments will occur at baseline (13-16 weeks gestation), 27-29 weeks gestation, 35-37 weeks gestation, and approximately 2 weeks postpartum. Safety assessments will be collected every 4 weeks after enrollment. Participants will be randomized within site (approximately 50 individuals at Pennington Biomedical Research Center and approximately 50 individuals at California Polytechnic University) and obesity to either: Provider Directed Group or Weight Maintenance Group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

盲法说明

Outcome assessments will be conducted by staff members who are masked to the participant's intervention group assignment.

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Are pregnant less than or equal to 15 weeks gestation at screening
  • •Have a body mass index between 31.0 and 55.0 inclusive
  • •Have a confirmed viable singleton gestation
  • •Willing to receive randomization to either group
  • •Willing and able to eat the study foods
  • •Willing to enroll infant for study measurements after birth
  • •Receive clearance from the prenatal care provider for participation

排除标准

  • •Smoking, drug, or alcohol use
  • •Have a known fetal anomaly
  • •Have a non-pregnancy related illness
  • •Have pre-existing diabetes
  • •Have pre-existing hypertension
  • •Have severe anemia
  • •Have current mental health issue or eating disorder
  • •Short inter-pregnancy interval (<6 months since last pregnancy)
  • •Use of assisted reproductive technology
  • •Use of medications with known effects on body weight including over the counter medications and supplements for weight loss
  • •History of pre-eclampsia, prior small for gestational age infant, bariatric surgery
  • •Planning to move out of the area in the next 12 months

研究组 & 干预措施

Weight Maintenance Group

Experimental

Individuals in this group will receive all aspects of the Provider Directed Group plus a comprehensive behavioral fat mass loss intervention with food provision. Individuals in this group will be provided foods to eat to support weight maintenance and loss of body fat throughout pregnancy. They will be asked to attend two behavioral counseling sessions at the beginning of the study to help learn the program and set goals. They will return for brief visits with a lifestyle counselor every two weeks until 20 weeks gestation and at least once a month until delivery. Individuals will be provided a scale to help keep track of weight during pregnancy.

干预措施: Weight Maintenance Group (Behavioral)

Provider Directed Group

No Intervention

Individuals in this group will receive what is standard practice by their prenatal care providers during pregnancy. In addition, individuals in this group will be asked to attend a brief session at the time of randomization to familiarize with the study and what is expected. They will also be provided with materials describing healthy behaviors in pregnancy.

结局指标

主要结局

Body weight

时间窗: From study entry to approximately 2 weeks postpartum

Body weight will be measured using a calibrated electrical scale with participants wearing a hospital gown and underwear.

次要结局

  • Fat mass(From study entry to approximately 2 weeks postpartum)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Leanne Redman

Professor

Pennington Biomedical Research Center

研究点 (3)

Loading locations...

相似试验