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临床试验/NCT02963428
NCT02963428已完成不适用

Teaching Appropriate Gestational Weight Gain

Geisinger Clinic2 个研究点 分布在 1 个国家目标入组 218 人开始时间: 2016年11月最近更新:
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
218
试验地点
2
主要终点
Gestational weight gain, adjusting for time in the study

研究概览

简要总结

The study aims to improve obstetrical care by managing gestational weight gain (GWG) among high risk women in an effort to reduce maternal and fetal complications.

详细描述

The project is aimed at teaching women about the appropriate weight gain during pregnancy to optimize health outcomes for mothers and newborn babies. Obese gravida meeting inclusion criteria and none of the exclusion criteria will be offered enrollment in TAGG. Those that consent will be randomized to receive standard of care or enhanced care regarding gestational weight gain.

The primary outcome is the proportion of patients that gain less than 20 lbs over the course of the pregnancy. Secondary outcomes include patient knowledge and expectations, attitude about pregnancy weight gain, self-efficacy of ability to eat healthy, and eating, sleeping and physical activity behavior, perceived stress, psychological factors, patient-experience, involvement in care, and food security.

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)

入排标准

性别
Female
接受健康志愿者

入选标准

  • Pre-pregnancy body mass index of at least 30 kg/m2 (per patient report of weight)
  • Less than 16 weeks gestation
  • Gestational weight gain (GWG) less than < 11 pounds from their pre-pregnancy weight to time of potential study enrollment
  • Singleton gestation
  • Access to a phone

排除标准

  • BMI less than 30 kg/m2
  • Gestational age greater than or equal to 16 weeks
  • Active diagnosis of cancer on their electronic health record problem list
  • Acquired immunodeficiency syndrome (AIDS)
  • Palliative medicine patients
  • Multiple gestations
  • GWG in excess of 11 pounds prior to study enrollment
  • Patients with Non-Geisinger prenatal care providers
  • Vegan diet
  • Malabsorptive conditions
  • Previously enrolled in TAGG during prior pregnancy. Patient will be excluded from re-randomization
  • Non-English Speaking

研究组 & 干预措施

Standard of Care (SOC)

No Intervention

Participants will receive the usual standard of care which includes written educational materials as well as counseling by their obstetric care provider.

Enhanced Care (EC)

Experimental

In addition to standard of care, the study participants will also receive:

i. An initial consult with a licensed, Registered Dietician Nutritionist (RDN); ii. Regular tele-health check-ups (10-20 mins/check-up) with the RDN until delivery; iii. Exposure to personal GWG chart; iv. Letter from physician stating the recommendations for GWG over the course of the pregnancy.

干预措施: Enhanced Care (Behavioral)

结局指标

主要结局

Gestational weight gain, adjusting for time in the study

时间窗: at delivery

次要结局

  • Perceived stress measured via Perceived Stress Scale(Baseline through 4-12 weeks postpartum)
  • Patient knowledge and expectations factors(Baseline, 32-34 Weeks Gestation, and 4-12 Weeks Postpartum)
  • Attitude on pregnancy weight gain(Baseline, 32-34 Weeks Gestation, and 4-12 Weeks Postpartum)
  • Neonatal intensive care unit (NICU) admissions(At Delivery)
  • Rate of gestational weight gain(Baseline through 4-12 weeks postpartum)
  • Patient-experience and involvement in care(Baseline, 32-34 Weeks Gestation, and 4-12 Weeks Postpartum)
  • Cost of Treatment(Baseline through 4-12 Weeks Postpartum)
  • Self-efficacy of healthy eating(Baseline, 32-34 Weeks Gestation, and 4-12 Weeks Postpartum)
  • Eating, sleeping and physical activity behavior(Baseline, 32-34 Weeks Gestation, and 4-12 Weeks Postpartum)
  • Diagnosis of gestational diabetes mellitus(Baseline through 4-12 Weeks Postpartum)
  • Delivery of large for gestational age infants(At Delivery)
  • Mode of delivery(At Delivery)
  • Psychological factors measured via Pregnancy Weight Gain Attitude Scale(Baseline through 4-12 Weeks postpartum)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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