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The Effects of Innatal Yoga Practices on Pain, Comfort, and Satisfaction in Primiparous Women

2026년 9월 20일 업데이트: Handan ASATEKİN

The aim of this study is to examine the effects of prenatal yoga practices on labor pain, comfort level during labor, and overall birth satisfaction in primiparous pregnant women in Turkey. This study, which will be conducted using a randomized controlled trial design, aims to measure both the physical contribution of prenatal yoga practice to the birthing process and its effects on psychological well-being and satisfaction, thereby providing evidence-based recommendations to improve the quality of childbirth services.

연구 개요

상태

아직 모집하지 않음

상세 설명

Childbirth is a significant turning point in a woman's life cycle, both physiologically and psychologically. For primiparous women, especially first-time mothers, this process can be filled with intense pain, uncertainty, anxiety, and stress. Research shows that 60% to 80% of women worldwide experience anxiety and fear during childbirth (Bharati, Pokhrel & Bhandari, 2024). A study conducted in Turkey found that 66.3% of pregnant women experienced high levels of fear related to labor pains. Fear of childbirth is not only a psychological experience but can also negatively impact the physiological functioning of the birthing process. Intense fear of childbirth can lead to prolonged labor, an increase in the preference for cesarean sections, and the development of problems such as postpartum depression or post-traumatic stress disorder. Furthermore, the negative impact of fear of childbirth on birth self-efficacy makes the birthing experience more challenging for primiparous women. Key causes of fear of childbirth include intolerance to pain, concern about harming the mother or baby, fear of losing control during labor, and distrust of healthcare personnel. These fears are experienced more intensely, especially in women who have never given birth before; comparative studies have found that primiparous women have significantly higher levels of fear compared to multiparous women. Negative emotions experienced during childbirth directly affect a mother's comfort during labor, her satisfaction with the birth, and her postpartum well-being. Although pain is a natural part of childbirth, how this process is managed, the mother's overall perception of childbirth, and its duration play a decisive role. According to the World Health Organization, the global cesarean section rate is 21%, while in Türkiye this rate has reached 58% (Turkish Statistical Institute, 2023). This situation once again emphasizes the importance of managing the fear of childbirth and pain. In conclusion, it appears that yoga practices help reduce fear of childbirth, contribute to women developing a positive perception of childbirth, and increase satisfaction with birth.

연구 유형

중재적

등록 (추정된)

74

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Mus Center
      • Muş, Mus Center, 터키 (Türkiye), 49250
        • Mus Alparslan University Campus, Diyarbakir Road 7th km, 49250 Mus Center/Mus,

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

여성

설명

Inclusion Criteria:

  • Volunteers to participate in the study,
  • Able to communicate in Turkish,
  • Literate,
  • Not diagnosed with any high-risk pregnancy,
  • Primiparous (first pregnancy),
  • In latent phase (dilation 0-5 cm) upon admission to the delivery room,
  • Not having a previous psychiatric diagnosis,
  • Pregnant women without any identified maternal or infant risk factors during their pregnancy.

Exclusion Criteria:

  • Pregnant women who give birth via cesarean section and do not meet the inclusion criteria will be excluded from the study.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 지지 요법
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: innatal yoga group

Primiparous pregnant women arriving at the hospital for delivery will be randomly divided into two groups after admission to the delivery room (latent phase) if they meet the sampling criteria. The pregnant women will be informed about the study and their consent obtained through face-to-face interviews conducted by the researchers. Pregnant women with cervical dilation between 0-5 cm who are randomly selected for the study will complete a Personal Information Form, the Numerical Rating Scale (MRS), the Verbal Category Scale (VCS), and the Birth Comfort Scale (BCS). The pregnant women will perform 8 different innatal yoga poses determined by the researchers, each pose lasting 5 minutes, for a total of 40 minutes. Following the yoga practice, a vaginal examination will be performed by the same midwife, and the MRS, VCS, and BCS will be administered again. After labor, the Birth Satisfaction Scale-Short Form (BSS-S) will be administered to the women.

Primiparous pregnant women with cervical dilation between 0-5 cm, who were randomly assigned to experimental and control groups, will be administered a Personal Information Form, the Numerical Rating Scale (MRS), the Verbal Category Scale (VCS), and the Birth Comfort Scale (BCS). Following this, only the pregnant women in the experimental group will perform 8 different yoga poses, each pose lasting 5 minutes, as determined by the researchers. Routine care will be provided to the control group. After the yoga session, a vaginal examination will be performed by the same midwife, and all pregnant women will be re-administered the MRS, VCS, and BCS. After labor, both the experimental and control groups will be administered the Birth Satisfaction Scale-Short Form (BSS-S).

간섭 없음: routine primiparous group

Primiparous pregnant women arriving at the hospital for delivery will be randomly assigned to two groups after admission to the delivery room (latent phase), provided they meet the sampling criteria. These women in the control group will be informed about the study and their consent obtained through face-to-face interviews conducted by the researcher. Pregnant women with cervical dilation between 0-5 cm who were assigned to the control group after randomization will complete the Personal Information Form, the Numerical Rating Scale (MRS), the Verbal Category Scale (VCS), and the Birth Comfort Scale (BCS). After receiving routine care, the same midwife will perform a vaginal examination on the pregnant woman 40 minutes later, and the MRS, VCS, and BCS will be administered again. Following labor, the Birth Satisfaction Scale-Short Form (BSS-S) will be administered to the pregnant women in the control group.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Yoga practices aim to reduce fear of childbirth, help women develop a positive perception of childbirth, and increase satisfaction with birth.
기간: From the 0-5 cm cervical dilation range to the early postpartum period (4-24 hours)

The DMÖ-K is a 10-item scale using a five-point Likert type. The scale is scored as follows: "Strongly agree" (4 points), "Agree" (3 points), "Undecided" (2 points), "Disagree" (1 point), "Strongly disagree" (0 points). Items 2, 4, 7, and 8 are reverse-calculated. The lowest possible score is "0", and the highest is "40"; higher scores indicate higher satisfaction levels.

From the 0-5 cm cervical dilation range to the early postpartum period (4-24 hours)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 11월 15일

기본 완료 (추정된)

2027년 12월 1일

연구 완료 (추정된)

2027년 12월 1일

연구 등록 날짜

최초 제출

2026년 6월 6일

QC 기준을 충족하는 최초 제출

2026년 9월 20일

처음 게시됨 (실제)

2026년 9월 24일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 24일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 20일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • MusAlparslanU-SBF-HAZ-002

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

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아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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