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临床试验/NCT06913582
NCT06913582已完成不适用

Chang Gung Medical Foundation Institutional Review Board

Chang Gung Memorial Hospital2 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2022年6月22日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
76
试验地点
2
主要终点
demographic data and exercise history of two groups

研究概览

简要总结

The goal of this quasi-experimental study design is to explore the effects of distance yoga learning in improving depression and pregnancy stress in pregnant women during the pandemic disease. The main questions which aim to answer are:

  1. hypothesis1 - Distance yoga learning can decrease depression during pregnancy.
  2. hypothesis2 -Distance yoga learning can decrease pregnancy stress. The experimental group received a 12-week pregnancy yoga program, including one weekly 60-minute distance yoga class and followed by 2 times of DVD yoga exercise at home while the control group received only routine nursing care.

详细描述

This is a quasi-experimental study design for primiparous women in the obstetrics and gynecology department of a regional hospital as the research subjects. This study received ethical approval from the hospital and all participants provided written informed consent. After the researcher took convenience samples and explained the research purpose in the prenatal parent classroom, they were assigned to the experimental group and the control group according to the wishes of the cases. Pregnant women in the experimental group received routine prenatal care guidance and yoga exercises three times a week, while the control group only received routine pre-natal guidance and the differences between the two groups were compared.

The sample size was estimated using G-power 3.1.9.2 software. The sample size was estimated to be 52 participants. Assuming the attrition rate was 20%, there were 32 people in the experimental group and the control group making a total of 64 participants.

During the study, one participant in the experimental group had premature delivery due to early water rupture, and the other one was hospitalized for tocolysis due to frequent uterine contractions and therefore withdrew from the experiment, resulting in a loss of 2 samples. For control group, one participant was admitted to the hospital for tocolysis due to prepartum hemorrhage and was withdrew from the study. Therefore, a total of 61 participants completed the study .

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

盲法说明

First-time mothers between 20 and 26 weeks of pregnancy

入排标准

年龄范围
22 Years 至 43 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • First-time mothers between 20 and 26 weeks of pregnancy.
  • normal fetus with a singleton.
  • no history of smoking, drinking, or drug abuse.
  • no bleeding during pregnancy.
  • no related high-risk complications during pregnancy (such as high blood pressure, preeclampsia, gestational diabetes, heart dis-ease, etc.).
  • no early abortion symptoms.
  • Able to move normally.
  • Able to listen, speak, read and write Chinese.
  • Able to participate in the research and cooperate in completing the questionnaire.

排除标准

  • Exclusion conditions (any one)
  • Multiparous women.
  • First-time mothers with pregnancy >26 weeks.
  • Multiple births.
  • Symptoms of bleeding or early miscarriage.
  • Related high-risk pregnancy complications.

结局指标

主要结局

demographic data and exercise history of two groups

时间窗: 12 months

Basic characteristics: Basic personal information included age, height, religious beliefs, marital status, education, daily activities, past medical history, etc. Obstetric variable information included weeks of pregnancy, pre-pregnancy weight, weight gained during pregnancy, and exercise before and during pregnancy, etc.

The change of depression status of two groups

时间窗: 12 months

Edinburgh Postnatal Depression Scale(EPDS): The Edinburgh Postnatal Depression Scale is used to measure prenatal and postpartum depressed mood. There are 10 questions in total, each question is scored on a 4-point scale. According to the order of each option, the first, second and fourth items are scored from 0 to 3 points, the other items are scored from 3 to 0 points, and the total score is from 0 to 30 points. The levels of scale were as follows: 0-9 points: low risk, usually no further psychological intervention is needed; 10-12 points: medium risk, further evaluation and observation are recom-mended; 13 points and above: high risk, comprehensive psychological evaluation and possible intervention measures should be carried out. The higher the score of pregnant women, the more severe the prenatal depression is.

Stress during pregnancy of two groups

时间窗: 12 months

Pregnancy Stress Rating Scale (PSRS): The "Pregnancy Stress Scale" developed by Chen, Huang, and Ka in 1991 and revised it into a new version of the "Pregnancy Stress Scale" by Chen was used in this study. The scale has five factors; it mainly measures the psychological stress experienced by women during pregnancy. There are 36 questions in total with the Likert five-point scoring method totaling score of 180 points. The higher the score, the greater the stress during pregnancy. The new version of the "Pregnancy Stress Scale" has good internal consistency (α=.92) and 2-week test-retest reliability (α=.82).

次要结局

未报告次要终点

研究者

发起方
Chang Gung Memorial Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Wen-Ping Lee

Head Nurse

Chang Gung Memorial Hospital

研究点 (2)

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