이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

비부하 검사 중 음악

2026년 10월 16일 업데이트: GAMZE GOKE ARSLAN, Karamanoğlu Mehmetbey University

비스트레스 검사 중 음악이 여성의 편안함, 생체 징후 및 불안에 미치는 영향: 무작위 대조 연구

Music has direct and indirect positive effects on the mother and fetus during pregnancy and perinatal period. This study was aimed at investigating effects of music played during the Non-Stress Test (NST) procedure on the mother's comfort, vital signs and anxiety.

연구 개요

상태

완전한

정황

연구 유형

중재적

등록 (실제)

173

단계

  • 해당 없음

연락처 및 위치

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

연구 장소

    • Central
      • Karaman, Central, 터키 (Türkiye), 70200
        • University District, 2076 Street, No: 11

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 (성인)

건강한 자원 봉사자를 받아들입니다

예

연구 대상 성별

여성

설명

Inclusion Criteria:

  • Women aged 18-45 years
  • Completion of at least the 32nd week of gestation
  • No pregnancy-related risk factors (e.g., premature rupture of membranes, preeclampsia, gestational diabetes)
  • No multiple pregnancy
  • Normal blood pressure levels (not ≤80/60 mmHg and not ≥140/90 mmHg)
  • Having eaten at least two hours before the NST procedure
  • No smoking or alcohol consumption for at least two hours before the NST procedure
  • Ability to communicate effectively
  • No hearing impairment
  • Voluntary participation in the study

Exclusion Criteria:

  • Pregnant women with fetal distress
  • Cases for whom the physician considered emergency intervention necessary
  • Individuals with an impaired NST requiring immediate intervention
  • Individuals with a diagnosed psychiatric disorder
  • Individuals with hearing impairment

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: Music Group

After the pregnant women were positioned, while the NST procedure was implemented they listened to music for 20-30 minutes. The pregnant women listened to the music on an MP3 player during the application. The duration of the music recorded on the MP3 player was 30 minutes. The music played to the pregnant women was selected by the researchers in accordance with the definition of relaxing music made in the literature. Before the music selection, the researchers communicated with the TÜMATA (Turkish acronym for the "Research and Promotion of Turkish Music Association). After the meeting held with the association, it was decided to use the 'Acemaşiran' (a musical mode in traditional Turkish music). In the study, music prepared by the TÜMATA in the Acemaşiran mode was played. It is stated that Acemaşiran mode helps balance the body, helps the listener relax, facilitates birth, helps correct the wrong position of the fetus in the womb, and has a pain and spasm relieving effect

The music played to the pregnant women was selected by the researchers in accordance with the definition of relaxing music made in the literature. Before the music selection, the researchers communicated with the TÜMATA (Turkish acronym for the "Research and Promotion of Turkish Music Association). After the meeting held with the association, it was decided to use the 'Acemaşiran' (a musical mode in traditional Turkish music). In the study, music prepared by the TÜMATA in the Acemaşiran mode was played. It is stated that Acemaşiran mode helps balance the body, helps the listener relax, facilitates birth, helps correct the wrong position of the fetus in the womb, and has a pain and spasm relieving effect.

간섭 없음: Control Group

Pregnant women were not subjected to any intervention during the NST procedure.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
During Non-Stress Testing on Women's Comfort Level
기간: Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)

Prenatal Comfort Scale (PCS) was used to determine women's comfort level. The short version of the PCS consists of 15 items. Response given to the items are rated on a six-point Likert type scale ranging from 0 to 5 (0 = Strongly disagree, 1 = Disagree, 2 = Undecided, 3 = Somewhat agree, 4 = Agree, 5 = Strongly agree). The minimum and maximum possible scores that can be obtained from the PCS are 0 and 75, respectively. The higher the score is the higher the comfort level is.

Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)
During Non-Stress Testing on Women's Systolic Blood Pressure Level
기간: Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)

The women's systolic blood pressure levels were measured with a calibrated electronic sphygmomanometer. Blood pressure levels are expressed in millimeters of mercury (mmHg).

Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)
During Non-Stress Testing on Women's Diastolic Blood Pressure Level
기간: Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)

The women's diastolic blood pressure levels were measured with a calibrated electronic sphygmomanometer. Blood pressure levels are expressed in millimeters of mercury (mmHg).

Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)
During Non-Stress Testing on Women's Heart Rate Level
기간: Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)

Heart rate level was determined electronically. Heart rate level was recorded in beats per minute (bpm).

Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)
During Non-Stress Testing on Women's Anxiety Level
기간: Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)

State Anxiety Scale (SAS) was used to determine the anxiety level. The scale is a 4-point Likert type, "not at all" (1), "somewhat" (2), "moderately" (3), "very much" (4). The scale consists of 20 items and items 1, 2, 5, 8, 10, 11, 15, 16, 19 and 20 are reverse scored. To calculate the total score of the SAS, the total score of the reversed items is subtracted from the total score of the non-reversed items. Then, 50 points, which is the constant value of the state anxiety scale, are added to this score. The result is the score for the overall SAS. The total score varies between 20 and 80. The higher the score is the higher the level of the anxiety is. While a score ranging between 0 and 19 indicates "no anxiety", a score ranging between 20 and 39 indicates mild anxiety, a score ranging between 40 and 59 indicates moderate anxiety, a score ranging between 60 and 79 indicates severe anxiety, and a score of 80 indicates very severe anxiety (Panic).

Pre-test: Before NST application Post-test: After NST application (Approximately 20-30 minutes after the NST session begins)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

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 (실제)

2025년 6월 1일

기본 완료 (실제)

2025년 8월 31일

연구 완료 (실제)

2025년 8월 31일

연구 등록 날짜

최초 제출

2025년 11월 23일

QC 기준을 충족하는 최초 제출

2025년 12월 9일

처음 게시됨 (실제)

2025년 12월 23일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 19일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 16일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • KMBU-NST-2025-01
  • 2169 (Ethics decision number) (기타 식별자: Non-Interventional Clinical Research Ethics Committee of the Republic of Türkiye Izmir Bakırçay University)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

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. .

구독하다