跳至主要内容
临床试验/NCT06187675
NCT06187675招募中不适用

A Participant Choice Approach to Improve Adherence and Investigate Pregnancy Outcomes to Lifestyle Interventions

Western University, Canada2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
2
主要终点
Adherence to the intervention strategy

研究概览

简要总结

Interventions that target excessive gestational weight gain (EGWG) with nutrition and exercise behavior change struggle with low program adherence. The investigators recently examined adherence in a randomized controlled trial to a previously established lifestyle program called the Nutrition and Exercise Lifestyle Intervention Program (NELIP) and found that those individuals with high adherence to the program were more likely to prevent EGWG. Perhaps offering participants a choice to intervention strategies may improve adherence. The current research question is: What impact does participant choice have on adherence to the introduction of nutrition and exercise components during 3 intervention strategies offered to pregnant individuals compared to no choice and does choice maintain pregnancy health outcomes? The strategies are: Group A - introducing both the nutrition and exercise components simultaneous at baseline (12-18 weeks of pregnancy) that is followed to delivery (NELIP); Group B - introducing the nutrition component first and then at 25 weeks adding the exercise component; or Group C - starting with the exercise component first, followed with introducing the nutrition component at 25 weeks. Both Groups B and C follow the full NELIP from 25 weeks to delivery (final intervention measures will occur at 34-36 weeks gestation). Follow-up will occur at birth (6-18 hours), 2, 6 and 12 months post delivery.

详细描述

Investigators are using a pseudo randomized yoked design and will include two groups: choice of intervention strategy or no-choice. If the individual is randomized to no choice, then the next person would get a choice and the no choice person would be assigned to the group yoked (matched) to the person with a choice. Participants assigned to the choice group will choose one of three intervention strategies provided; either Group A (receiving both nutrition and exercise simultaneously), B (starting with nutrition and receiving exercise sequentially followed by nutrition starting at 25 weeks) or C (starting with nutrition first and then introducing exercise sequentially at 25 weeks). All groups will follow the full NELIP until delivery. Participants in the no-choice group will be yoked (matched) to a participant in the choice group and receive the strategy that their yoked counterparts chose.

Nutrition component of NELIP: This component is a modified gestational diabetic meal plan that has four general goals tailored to the participant: (1) to achieve approximately 2000 kcal of energy per day. The determination of the amount of kcal consumed per day will consider the participant's intake from the dietary assessment. There also must not be a restriction of calories that exceeds 30% of their total energy intake; (2) participants will consume approximately 200-250g/day of carbohydrates, accounting for approximately 40-55% of total energy intake. Carbohydrate intake will be distributed throughout three meals and four snacks daily. The nutritionist will educate participants about the importance of complex and low-glycemic index carbohydrates through the one-on-one session; (3) fat and protein intake will be approximately 30% and 20-30% of total energy intake, respectively; (4) achieve appropriate micronutrient and fluid intake for pregnancy. This will be monitored by a weekly 24 hour food intake record.

Exercise component of NELIP: This is a walking program that comprises of 1 weekly supervised session on a treadmill or outside and participants will be recommended to walk 2 to 3 additional times per week. The walking program will start at 25 minutes per session, 3 to 4 times weekly, and increase by 2 minutes per week until 40 minutes and then maintained until delivery. This will be monitored by a wrist monitoring device. The primary outcome is adherence measured weekly using a published adherence protocol using a point system. Secondary outcomes are participant satisfaction to the program and health outcomes: weekly weight gain, calculated EGWG, and pregnancy outcomes (birth weight length, infant anthropometrics, APGAR scores and delivery complications). At 2, 6 and 12 months of age the maternal-infant dyad will return to the lab and infant morphometric measurements recorded from birth will be repeated.

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

data analysis will be analysed blinded to group

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • between 12 to 18 weeks of pregnancy
  • a singleton fetus
  • medically screened with the Get Active Questionnaire for Pregnancy to determine eligibility for participation in the exercise component

排除标准

  • inability to walk
  • serious medical problems
  • high blood pressure
  • uncontrolled chest pain
  • uncontrolled symptomatic lung disease
  • diabetes before pregnancy
  • a history of recreational substance use disorder
  • any contraindication to exercise
  • enrolled in another clinical trial.

结局指标

主要结局

Adherence to the intervention strategy

时间窗: Measured once per week from baseline (12-18 weeks gestation) to end of the intervention (34-36 weeks gestation)

Percent of participants adherent to the strategies measured by a published Adherence Scale giving a score out of 3 for each component (nutrition and exercise).

次要结局

  • Pregnancy complications(Measured within 6 to 18 hours after delivery)
  • Postpartum body weight(2, 6 and 12 months after birth)
  • Gestational weight gain(Measured weekly from 12-18 weeks of pregnancy to 34-36 weeks of pregnancy)
  • Participant satisfaction(Measured at 34-36 weeks of pregnancy at the end of the intervention)
  • Birth weight(Measured within 6 to 18 hours after delivery)
  • Birth length(Measured within 6 to 18 hours after delivery)
  • Follow-up Infant weight(2, 6 and 12 months after birth)
  • Follow-up Infant length(2, 6 and 12 months after birth)
  • Pregnancy outcome(Measured within 6 to 18 hours after delivery)
  • Birth circumferences(Measured within 6 to 18 hours after delivery)
  • Birth skinfolds(Measured within 6 to 18 hours after delivery)
  • Follow-up Infant Girths(2, 6 and 12 months after birth)
  • Follow-up Infant adiposity(2, 6 and 12 months after birth)

研究者

发起方
Western University, Canada
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michelle Mottola

Principal Investigator

Western University, Canada

研究点 (2)

Loading locations...

相似试验