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临床试验/NCT04298125
NCT04298125招募中不适用

Antenatal Factors Impacting Obesity and Metabolism in Children: Sub-objective 2D

Arkansas Children's Hospital Research Institute1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年7月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
Acceptability of Intervention Measure: 38 weeks

研究概览

简要总结

The Expecting intervention as delivered in prior studies in a clinical setting is described in a previous approved IRB submission (Protocol 202954). The current project will seek to engage community stakeholders to translate Expecting to a community-delivered intervention and to test its acceptability, feasibility, and fidelity in a proof of principle study with 60 expecting mothers.

详细描述

The aim of this study is to adapt and determine acceptability, feasibility and fidelity of the research- clinic-based Expecting intervention with pregnant women with obesity in community settings. Specifically, the investigators will show effective application of the Replicating Effective Programs (REP) framework (e.g., fidelity, feasibility, acceptability) to translate the research clinic-based intervention to community settings. REP provides a four-phase process for implementing evidence-based interventions and has demonstrated effective application to translate clinical interventions to community settings. Built into the REP framework is the collection of feedback from community stakeholders, iterative piloting of the intervention in the community, and a process for standardizing the intervention across community settings. Following adaptation, the updated intervention will be piloted. The pilot study will include 60 expecting women. The investigators will randomize half to receive the community-adapted Expecting intervention (Intervention, N=30) and half to receive standard of care (Control, N=30).

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

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

入选标准

  • •(a) Body Mass Index > 30,
  • •(b) singleton pregnancy,
  • •(c) between 11-15 weeks of pregnancy (at enrollment),
  • •(d) Do not currently meet recommended guidelines of 150 min of activity per week
  • •(e) cleared by physician

排除标准

  • •(a) contraindications for exercise (preeclampsia-eclampsia, premature rupture of the membranes, antepartum hemorrhage, placenta previa, multiple gestation and other defined conditions)
  • •(b) illicit drug use.

研究组 & 干预措施

Exercise in Pregnancy in Community

Experimental

The Expecting intervention at the ACNC includes three 30-45 minute, in-person exercise sessions per week. The sessions are gradually increased in length over the first weeks of participation, and are comprised of 15-30 minutes of moderate aerobic activity (recumbent bike, walking on a treadmill or on an elliptical machine) as well as 5-10 minutes of resistance training using hydraulic exercise equipment. The sessions conclude with stretching exercises. Throughout the session, a personal trainer assesses the rating of perceived exertion using the 6 to 20 point Borg scale of exhaustion.41 Between sessions, participants are asked to monitor their daily step count with a target of 10,000 steps per day using a pedometer provided to the participant. This number is reported to or downloaded by the personal trainer at each in-person session. These elements will be adapted to provide a similar exercise experience that is accessible to women in their local community.

干预措施: Exercise in Pregnancy (Behavioral)

Standard Care

No Intervention

Participants will receive guidance on exercise from their physician as usual.

结局指标

主要结局

Acceptability of Intervention Measure: 38 weeks

时间窗: 38 weeks

Attitudinal Implementation Outcome on a 1 to 5 scale

Feasibility of Intervention Measure:38 weeks

时间窗: 38 weeks

Attitudinal Implementation Outcome on a 1 to 5 scale

次要结局

  • Total Cholesterol from Lipid Panel(Change from Baseline to Delivery and 6 Months Post Delivery)
  • Body Mass Index(Change from Baseline to Delivery and 6 Months Post Delivery)
  • Number of intervention sessions completed(15 weeks through 38 weeks)
  • Blood Pressure(Change from Baseline to Delivery and 6 Months Post Delivery)
  • Number of minutes of physical activity(Change from Baseline to Delivery and 6 Months Post Delivery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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