Heat Application to the Sacral Region and Pain Level During the First Stage of Labor
- Conditions
- Duration of LaborHeat ExposureLabor PainApgar Score
- Interventions
- Other: heat application
- Registration Number
- NCT06297031
- Lead Sponsor
- Istanbul Demiroglu Bilim University
- Brief Summary
The aim of this study was to determine the effect of hot application applied to the sacral region during first stage of labor on women's pain level and labor process.
- Detailed Description
It is stated that the pain experienced during labor, which is a physiological process, creates stress and anxiety in women and increases the risk of maternal and neonatal complications. Therefore, keeping labor pain under control is important from an obstetrical perspective. Pain experienced during labor is caused by dilatation of the cervix and uterine contractions, and occurs in different regions at each stage of labor. Due to the descent of the fetal head into the pelvis and the pressure it puts on the lumbosacral plexus, the mother feels pain in her back, waist, legs and hips, especially in the first stage of labor. Although pharmacological and non-pharmacological methods are used in the management of labor pain, they have disadvantages such as experiencing drug-related side effects due to pharmacological methods, causing undesirable effects in the woman and the fetus, the woman not being able to actively participate in the labor and not being able to remember what happened during labor.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 134
- Women were over 18 years of age
- Primipara
- Volunteered to participate in the study
- Were in the latent phase of labor (cervical dilatation 1-2 cm)
- Had a single fetus in vertex presentation
- Had no history of pregnancy complications
- Had not undergone any intervention in the sacral region were included in the study
- Applied pharmacological pain control methods in the first stage of labor
- Had a cesarean section decision at any stage
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description heat application heat application women in the intervention group were treated with hot water application to the sacral region during the first stage of labor. When the cervical dilatation was 3-4 cm, 5-6 cm and 7-8 cm, heat application was applied a total of 3 times.
- Primary Outcome Measures
Name Time Method Change From Baseline labor Pain at three times The pain was evaluated three times during labor It will be assessed three times during the first stage of the labor with Number Rating Scale. Pain intensity measured on a Number Rating Scale with scores ranging from 0 - 10. Pain increases as the score increases. The high point describes bad outcome.
- Secondary Outcome Measures
Name Time Method Change From Baseline Fetal Heart Rate A total of three measurement results were obtained (after the cervical dilatation was evaluated as 3-4 cm, 5-6 cm and 7-8 cm) after the cervical dilatation Fetal Heart Rate was evaluated with monitor. the recommended level is 100 to 160 heart beat/minute
Change From Baseline APGAR score after delivery After delivery in two times at first and fifth minutes through study completion, an average of 1 day The scale is designed to determine the need for urgent intervention by assessing the condition of the newborn in order to reduce neonatal morbidity and mortality rates. A score of 0 represents the lowest level of functionality, while a score of 10 indicates optimal health. A score below 4 indicates that the newborn has significant respiratory distress that requires urgent medical attention
Duration of the first stage of labor through study completion, an average of 1 day The time between the start of the pain expressed by the woman and the moment she was taken to the delivery table was calculated by the researcher and called the first stage of labor. The researcher used clock to calculate the duration
Trial Locations
- Locations (1)
Demiroglu Bilim University
🇹🇷Istanbul, Turkey