The Effect Of Partner-Assısted Rebozo Technıque On Labor Paın And Satısfactıon In Prımary Pregnant Women
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 64
- 试验地点
- 1
- 主要终点
- Labor Pains
研究概览
简要总结
The main objective of this study is to examine the effect of the rebozo technique, applied with partner support, on labor pain and birth satisfaction in primiparous pregnant women. This research is planned as a randomized controlled experimental study. A total of 64 pregnant women, 32 in the control group and 32 in the experimental group, who meet the sample selection criteria and agree to participate in the study, will constitute the sample of the study. Participants included in the study will be administered the Informed Consent Form, the "Demographic Information Form" created by the researcher, the "Fathers' Participation in Birth Scale", VAS scoring, "Birth Care Guide", "Observation Form Regarding Labor" and the "Birth Satisfaction Scale". Data will be analyzed using appropriate statistical methods. It is expected that the results obtained will contribute to the use of non-pharmacological methods in the birthing process and the support of partner participation.
详细描述
This study investigates the effect of the rebozo technique, applied with partner support, on labor pain and satisfaction in primiparous pregnant women. It is a planned study involving a total of 64 participants. The data will be recorded three times after the pregnant woman reaches 5 centimeters of active labor in the first stage. There are two separate groups: a control group and an experimental group. Three follow-up observations will be conducted in both groups using the defined procedures, and the data will be recorded.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 49 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Those aged between 18 and 49,
- •Between 37-42 weeks of gestation,
- •Primiparous pregnancy,
- •In head presentation, the fetus is singular,
- •Those who have not been diagnosed with a high-risk pregnancy,
- •Someone who understands and can speak Turkish,
- •In the active phase (5cm and above),
- •The spouse is allowed to be present at the birth.
排除标准
- •Those who experienced adjustment problems in the study,
- •Patients who require an emergency cesarean section,
- •Pregnancy with a known high-risk diagnosis (IUGR, fetal anomaly, polyhydramnios or oligohydramnios, presentation anomaly, multiple pregnancy, preeclampsia, etc.)
研究组 & 干预措施
Control Group
In primiparous pregnant women in the active phase, routine midwifery care will be applied, and VAS scoring will be performed according to the stages of cervical effacement and dilation (3 times: 5cm, 6-8cm, 9-10cm).
Experimental Group
The labor process will be recorded in the "Birth Care Guide" by the attending midwife, and routine midwifery care and rebozo technique will be applied. When dilation reaches 5 cm, a VAS I assessment will be performed on the pregnant woman before applying the rebozo technique, and cervical effacement, dilation, FHR, vital signs, head level, number and duration of contractions will be recorded in the "Birth Care Guide". Rebozo will be applied for 10 minutes between contractions using the technique chosen by the pregnant woman. 30 minutes after rebozo application, a VAS II assessment will be performed, and cervical effacement, dilation, FHR, vital signs, head level, number and duration of contractions will be recorded in the "Birth Care Guide". The same procedure will be applied when dilation reaches 6-8 cm and 9-10 cm.
干预措施: Rebozo Technique (Other)
结局指标
主要结局
Labor Pains
时间窗: The VAS pain assessment scale is a measurement used to evaluate labor from the active phase (5 cm) to the completion of the first stage (10 cm). The VAS pain score will be used from the beginning of active labor (5 cm) until the moment of birth (10 cm).
The VAS pain score is used to assess labor pain, and pain intensity is rated on a scale of 0 to 10. 0 indicates no pain, while 10 indicates unbearable pain.
Birth Satisfaction
时间窗: The birth satisfaction scale is an assessment scale administered to women who have completed childbirth, within the first 24 hours after delivery.
The Birth Satisfaction Scale is used to assess birth satisfaction. This scale is a measurement tool administered to women who have had vaginal deliveries during the postpartum period. It consists of three sub-dimensions and a total of 10 items. The scale is a 5-point Likert-type scale, with options ranging from 0 (strongly disagree), 1 (disagree), 2 (neutral), 3 (agree), and 4 (strongly agree).
次要结局
未报告次要终点
研究者
Beyza Halaç Bozkurt
MIDWIFE
Istanbul Saglik Bilimleri University