Non Stress Test and Music Performance

  • STATUS
    Recruiting
  • days left to enroll
    51
  • participants needed
    139
  • sponsor
    Ataturk University
Updated on 4 October 2022

Summary

Today, many methods are used in the evaluation of intrauterine fetal well-being. Non-stress test (NST) method is mostly used in the non-invasive evaluation of fetal well-being during pregnancy and labor. NST is a procedure in which fetal heart sounds are recorded and the relationship between fetal movements and fetal heart beat is monitored.3 Various methods are used to minimize the psychological effects that occur during pregnancy. Among these methods, it has been seen in the studies in the literature that music, which is a non-pharmacological method, has a positive effect on the pregnant woman and the fetus. It is easy and enjoyable to listen to music during the routine non-stress test process. However, there are not enough studies to prove the effect of music.

The aim of this study was to examine the effects of the music concert applied during the nonstress test procedure on the health of the fetus, the anxiety level of the pregnant woman and blood pressure.

Description

expected

Details
Condition Fetal Health, Pregnancy Related
Treatment music terapy
Clinical Study IdentifierNCT05325840
SponsorAtaturk University
Last Modified on4 October 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Become literate
Be in the 18-45 age range
Being at the 32nd and above gestational week
Not carrying any risk factors during pregnancy (preeclampsia, IUGR, gestational diabetes, etc.)
Have eaten at least two hours before the NST procedure
No fetal defined cardiovascular disease
The pregnant woman is open to communication and does not have mental or mental problems
Absence of auditory problems

Exclusion Criteria

Absence of illiteracy of the pregnant woman
Uterine contraction in NST
Pregnant women who need fetal distress and urgent intervention by the physician
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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