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The comparison of two methods of music listening, by mother and fetus on the non-stress test outcome.

Not Applicable
Conditions
onstress testing in pregnant women.
expesure to the vibration
Registration Number
IRCT201112108362N1
Lead Sponsor
Vice Chancellor for research Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
213
Inclusion Criteria

age range 35-18 years; gestational age 37- 40 weeks of pregnancy; singleton pregnancy; Women with uncomplicated pregnancies include: hypertension disorders, diabetic women requiring insulin, women suspected fetal inter uterine growth restricted, Women after 41 gestational age determinate by last menstruation date or ultrasound 16 to 20 weeks, premature rupture of membranes, multiple pregnancies, intrauterine death fetus, the embryonic lethal anomalies, fetus by cardiovascular anomalies, amniotic fluid disorders, the fetus was diagnosed with anencephaly; baseline of heart rate between 160-110; No pregnant women by loss- hearing; no anatomic or mental disorders in mother (psychosis, schizophrenia, and uterine abnormalities); no chronic disease in mother such as heart disease, lung, kidney, chronic hypertension and diabetes; Not smoking and tobacco; not strenuous physical activity until two hours before the test; no use of analgesics, narcotics, sedative and effected drugs on uterine contractions; Before entering the study vibroacoustic stimulation, glucose or fruit juice is not used; at least 1.5 is the last time the mere promise of a meal; no nonreactive non-stress test; no experience in music education; The written consent form. Exclusion criteria: any problem occurred during the study, including placenta abruption, and cord prolapsed; not wanting to continue more; more than three positive non-stress test (non-reactive); presence of uterine contractions.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The number of acceleration of fetal heart rate. Timepoint: Initial 10 minuts of test, second 10 minuts of test. Method of measurement: Toito Japanese model by fetal echocardiography.
Secondary Outcome Measures
NameTimeMethod
Reduce of time of nonstress testing. Timepoint: Initial 10 minuts of test, second 10 minuts of test. Method of measurement: Toito Japanese model by fetal echocardiography.
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