此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Development of a Multidimensional Predictive Model of Dystocic Labor. Association of Physical Condition and Psychosocial Factors With the Birth Process and Breastfeeding Success. (MPM-PD)

2026年6月18日 更新者:Aloma Antolí Forner、Institut Investigacio Sanitaria Pere Virgili

Development of a Multidimensional Predictive Model of Dystocic Labor (MPM-PD): Pilot Study on the Association of Physical Condition and Psychosocial Factors With the Completion of Labor and the Success of Breastfeeding.

The goal of this observational study is to learn how a pregnant woman's physical fitness and emotional well-being can help predict the type of birth she will have (such as a natural vaginal birth versus a cesarean section or a birth requiring medical assistance). The study focuses on pregnant women in their third trimester (after 28 weeks of pregnancy).

The main questions the study aims to answer are:

  • Can simple tests of physical strength and questions about emotions (like fear of childbirth) help health professionals predict if a birth might have complications or lack of progress?
  • Do a woman's physical activity and confidence levels during pregnancy affect her ability to successfully breastfeed her baby for up to 6 months?

Participants will be asked to:

  • Perform two simple physical tests during a clinic visit: a hand-grip test (dynamometry test) and a test to see how many times they can stand up from a chair in 30 seconds (Chair Stand Test, CST).
  • Complete surveys about their daily physical activity (PPAQ-S), their feelings and fears regarding childbirth (WDEQ-A), and how confident they feel about handling the final stage of birth and the pushing phase (CBSEI-16).
  • Answer brief follow-up phone calls one month and six months after the birth to talk about how breastfeeding is going.

研究概览

研究类型

观察性的

注册 (估计的)

420

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Tarragona
      • Tortosa、Tarragona、西班牙
        • 招聘中
        • Hospital de Tortosa Verge de la Cinta

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

The study population consists of pregnant women receiving prenatal care at the Hospital Universitari de Tortosa Verge de la Cinta (HUTVC).

The sample includes healthy volunteers in their third trimester of pregnancy (>28 weeks of gestation) with low-to-moderate obstetric risk. The population reflects a diverse group of expectant mothers who are able to perform simple physical functional tests and are interested in contributing to research on birth outcomes and breastfeeding. Participants are selected during their routine third-trimester prenatal visit at the HUTVC through non-probabilistic consecutive sampling until the required sample size of 420 participants is reached.

描述

Inclusion Criteria:

  • Pregnant women aged 18 years or older
  • Low-to-moderate risk pregnancy
  • Singleton pregnancy
  • Third trimester of pregnancy (>28 gestational weeks)
  • Understanding of the official languages
  • Acceptance and signing of the participant information sheet and informed consent form
  • Availability of an electronic device to complete the forms

Exclusion Criteria:

  • Medical contraindication for light physical activity
  • Severe cardio-respiratory or musculoskeletal pathology
  • Elective cesarean section
  • Severe fetal malformations

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Mode of birth
大体时间:At the time of delivery.
Classification of the birth outcome as either eutocic vaginal birth (spontaneous) or dystocic birth (including instrumental vaginal delivery or unplanned cesarean section).
At the time of delivery.

次要结果测量

结果测量
措施说明
大体时间
Breastfeeding maintenance.
大体时间:At 1 month and 6 months postpartum.
Status of exclusive or partial breastfeeding.
At 1 month and 6 months postpartum.

其他结果措施

结果测量
措施说明
大体时间
Duration of labor phases.
大体时间:From the onset of dilation until birth.
Time in minutes for the dilation and pushing stages of labor.
From the onset of dilation until birth.
Success of labor induction.
大体时间:During the hospital stay for delivery.
Proportion of induced labors that result in a vaginal birth.
During the hospital stay for delivery.
Prevalence of fear of childbirth (Tokophobia).
大体时间:During the third trimester of pregnancy (baseline assessment).
Score obtained through the Wijma Delivery Expectancy/Experience Questionnaire (WDEQ-A).
During the third trimester of pregnancy (baseline assessment).

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年6月10日

初级完成 (估计的)

2027年6月1日

研究完成 (估计的)

2027年12月1日

研究注册日期

首次提交

2026年6月3日

首先提交符合 QC 标准的

2026年6月3日

首次发布 (实际的)

2026年6月9日

研究记录更新

最后更新发布 (实际的)

2026年6月23日

上次提交的符合 QC 标准的更新

2026年6月18日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual Participant Data (IPD) will not be shared. The informed consent approved for this observational study does not include provisions for sharing individual participant data with external researchers.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅