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Sacral Massage With a Tennis Ball on Labor Pain and Comfort During the Intrapartum Period

Not Applicable
Not yet recruiting
Conditions
Pain Management
Birth Comfort
Massage Effect
Labor Pain
Registration Number
NCT06898580
Lead Sponsor
Istanbul University - Cerrahpasa
Brief Summary

Although pregnancy and labor are physiological events, the pain caused by uterine contractions during labor is among the most severe pains. This causes many women to fear labor. For this reason, control of labor pain should be one of the main goals of the care given to women in labor. Therefore, this study was designed to determine the effect of sacral massage with a tennis ball on labor pain and labor comfort in the intrapartum period.

Detailed Description

Pregnant women hospitalized in the maternity unit will be evaluated for compliance with the inclusion criteria. Women who meet the inclusion criteria and are willing to participate in the study will be randomized according to the simple random numbers table and the study group will be determined by the researcher by drawing lots. The purpose and stages of the study will be explained verbally to the women whose group is determined and the women will be asked to read and sign the Informed Voluntary Consent Form. Then, the Pregnancy Identification Form will be filled in by the researchers using the face-to-face interview method. Then the massage will be explained to the pregnant women in the experimental group and they will be asked to evaluate the Visual Analog Scale (VAS) before the procedure. While performing this application, the researcher will apply pressure to the sacral region with a tennis ball in a circular motion in a way that the patient can feel but not feel pain. The application will be applied to the pregnant woman for a total of 3 contractions. 30 minutes after each procedure, the woman will be asked to mark the intensity of the pain she feels on the VAS scale and to mark the Birth Comfort Scale.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
140
Inclusion Criteria
  • To be able to read and write Turkish,
  • Being over 18 years old
  • Being primiparous
  • Singular foetus and head presentation
  • Pregnancy at term (37-42 weeks)
  • Those without risk factors during pregnancy
  • Being in the active phase of labour in stage 1
  • Women without any chronic diseases
  • Those without a diagnosed psychiatric illness
  • To agree to participate in the research
Exclusion Criteria
  • If the participant wishes to leave the study voluntarily
  • Administration of any analgesic medication to reduce pain during labour
  • Development of any of the unexpected maternal-fetal risk conditions during labour
  • Having a caesarean section for any reason
  • The pregnant woman has spine and bone structure problems.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Labor painCervical dilatation will assses from 5-6 cm, 7-8 cm and 9-10 cm until delivery.

Visual Analog Scale (VAS) is a scale to measure pain and other subjective symptoms. It was as first introduced by Hayes and Patterson in 1921. The Scale maximum point is 10 and minimum point is zero. And as the scale score increases, the pain measure also increases.When cervical dilatation is 5-6 cm, the pregnant woman is asked to mark her pain score on a VAS (Visual Analog Scale) score from one to ten, and then massage is applied. After 30 minutes of massage, the pregnant woman is asked to rate the pain score on the VAS (Visual Analog Scale).

Secondary Outcome Measures
NameTimeMethod
birth comfortCervical dilatation will assses from 5-6 cm, 7-8 cm and 9-10 cm until delivery.

Childbirth Comfort Questionnaire is a scale for assessing childbirth comfort. The validity and reliability of the scale was made by Potur et al. in 2014. The Scale maximum point is 45 and minumum point is nine. And as the scale score increases, the comfort level also increases.

When cervical dilatation is 5-6 cm, the pregnant woman is asked to check the appropriate options on the 9-item scale on the CCQ. We want this procedure to be done three times in total when the pregnant woman is 5-6 cm, 7-8 cm and 9-10 cm.

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