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Clinical Trials in Turkey / NCT05488704
Active, not recruiting Observational

The Effect of Nonstress Test Device Noise Level on Stress Parameters in Primiparous Pregnant Women

NCT05488704 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2021-02-01
Last updated
2022-08-04

Condition(s) studied

StressNoise ExposurePrenatal StressPrenatal Care LatePregnancy Related

Investigational drug(s) / intervention(s)

Stress Parameters Measurement

Stress Parameters Measurement: Pre-Test (0-2 minutes before NST starts) - Measurement of vital parameters (Pre-Test) * Glucose measurement * Taking Salivary Cortisol and Saliva ACTH samples * Filling the Spielberger State Anxiety Inventory • Starting NST by controlling the noise level Interim Test-(NST 10th minute) - Measurement of vital parameters (Intermediate Test) * Taking Salivary Cortisol and Saliva ACTH samples * Filling the Spielberger State Anxiety Inventory • Termination of NST after 20 minutes Final Test(within 0-2 minutes after NST is over) * Measurement of vital parameters * Glucose measurement * Taking Salivary Cortisol and Saliva ACTH samples * Filling the Spielberger State Anxiety Inventory After Data Collection - Recording of data * Centrifugation and analysis of saliva samples taken

Study summary

Introduction: Prenatal tests can increase the stress levels of pregnant women. One of the tests performed to evaluate fetal health during pregnancy is the Nonstress Test (NST).

Objective: To evaluate the effect of NST device noise level on stress parameters in primiparous pregnant women.

Method: A randomized controlled, prospective study was conducted with 44 pregnant women in a State Hospital in Istanbul/Turkey between 01.02.2021 and 01.10.2021.

Personal Information Form, Spielberger State Anxiety Inventory, Hillrom Welch Allyn Connex Spot Monitor, Gluco Dr Glucometer, Extech SL 400 Personal Noise Dosimeter, Sennheiser HD 450BT ANC Over-Ear Bluetooth Headset, Eppendorf Tube, Philips Avalon FM20 NST were used to collect data. A p value of \<.05 was considered significant in the statistical evaluation.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * Voluntarily agreeing to participate in the research, * Over 18 years old, * Literate, * Fluent in Turkish * 32-42 of your pregnancy. in the week, * Having a healthy pregnancy, * No adrenal insufficiency, * No problems with hearing, * No psychiatric diagnosis during or before pregnancy, * No history of infertility, * Coming to routine pregnancy and NST control, * Have not had any food or drink for at least two hours before the procedure, * Primiparous pregnant women without contractions were included. Exclusion Criteria: * Pregnant women whose contractions are detected during the NST procedure, * Pregnant women with deceleration detected in the NST procedure were excluded from the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bakırköy Dr. Sadi Konuk Training and Research Hospital Istanbul Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05488704 on ClinicalTrials.gov ↗ ← All trials in Turkey