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临床试验/NCT06779903
NCT06779903已完成不适用

Effect Of Psychoeducatıon Interventıon For Postpartum Care On Postpartum Depressıon And Breastfeedıng

Eskisehir Osmangazi University1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2024年11月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
102
试验地点
1
主要终点
Antenatal Breastfeeding Self-Efficacy Scale

研究概览

简要总结

This study was planned to evaluate the effects of psychoeducation intervention for postpartum care on postpartum depression and breastfeeding.

详细描述

The pregnant women included in the sample were informed about the study and their written informed consent was obtained. Six interviews were conducted with the pregnant women, four at one-week intervals before birth, and one on the tenth day and sixth week after birth. These interviews were conducted with the women one-on-one and face-to-face.Women in the control group were not given any treatment other than routine care at family health centers. The psychoeducation program was applied to the women in the intervention group in six interviews.

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 (Participant)

盲法说明

control group (55) intervention group (55)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Women who are at the gestational age,
  • •over 18 years of age,
  • •planning to breastfeed,
  • •have no visual,
  • •hearing or mental disabilities,
  • •have a healthy fetus on ultrasonography

排除标准

  • •Women with depression and other mental illnesses diagnosed by a physician,
  • •those taking medication related to their mental illness,
  • •those who gave birth prematurely,
  • •those with contraindications to breastfeeding and newborns (head and spine anomalies such as anencephaly/spina bifida, having a fetus with brain anomalies such as hydrocephalus/microcephaly, active substance use or HIV diagnosis, etc.),
  • •those who were included in the study in the 3rd trimester but whose birth weight was less than 2500 grams,
  • •those whose babies were taken to the neonatal intensive care unit due to any postpartum complications and those who had premature babies (born before 37 weeks of gestation),
  • •those who did not participate in more than one interview

研究组 & 干预措施

intervention group

Active Comparator

The pregnant women included in the sample were informed about the study and their written informed consent was obtained. Six interviews were conducted with the pregnant women, four at one-week intervals before birth, and one on the tenth day and sixth week after birth. These interviews were conducted with the women one-on-one and face-to-face. psychoeducation program was applied to the women in the intervention group in six interviews.In the first interview, the psychoeducation intervention program booklet based on the Watson Model for postpartum care was given to the women and the interview was conducted within the scope of the program. The psychoeducation intervention program sessions based on the Watson Model for postpartum care in the study were conducted according to the WİBM improvement processes and psychoeducation techniques. The interviews lasted between 90 and 120 minutes on average.

干预措施: the psychoeducation intervention program booklet (Other)

control group

Placebo Comparator

The pregnant women included in the sample were informed about the study and their written informed consent was obtained. Six interviews were conducted with the pregnant women, four at one-week intervals before birth, and one on the tenth day and sixth week after birth. These interviews were conducted with the women one-on-one and face-to-face.Women in the control group were not given any treatment other than routine care at family health centers. In routine care, pregnant women were subjected to edema, varicose veins, weight, blood pressure, pulse, laboratory findings, baby heart sounds, medication intake, chronic disease follow-up and vaccination. Pregnant women were provided with counseling if they had any questions. Postpartum women were subjected to blood pressure, fever, pulse, bleeding and laboratory findings follow-up and were provided with counseling if they had any questions.

干预措施: routine care (Other)

结局指标

主要结局

Antenatal Breastfeeding Self-Efficacy Scale

时间窗: 1 day (first meeting during pregnancy)

The scale consists of a total of 20 items. The scale is a 5-point Likert type. The lowest score that can be obtained from the scale is 20 and the highest score is 100. An increase in the score obtained from the scale indicates that the perception of breastfeeding self-efficacy has increased.

Edinburgh Postpartum Depression Scale

时间窗: 1 day (first meeting during pregnancy and at the sixth week postpartum)

It is a 10-item self-report scale that measures maternal depressive symptoms over the past seven days. Higher scores reflect more depressive symptoms. Symptoms are rated on a 4-point Likert scale with scores ranging from 0 to 30. The cut-off score of the scale was determined as ≥13. If the total score of the scale is 12 or less, the participant is not at risk for PPD, but if he scores 13 or more, he is at risk.

Postpartum Breastfeeding Self-Efficacy

时间窗: sixth week postpartum

Breastfeeding Self-efficacy Short Form is a 5-point Likert-type scale. The lowest score that can be obtained from the scale is 14 and the highest score is 70. A higher score indicates higher breastfeeding self-efficacy.

Personal Information Form

时间窗: 1 day (first meeting during pregnancy)

The form created to determine the socio-demographic characteristics of the individuals included in the research was prepared by the researcher in line with the literature.

次要结局

未报告次要终点

研究者

发起方
Eskisehir Osmangazi University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yasemin Ozhuner

Principal Investigator

Eskisehir Osmangazi University

研究点 (1)

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