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Ney Music During Non-Stress Test and Maternal Anxiety

Effect of Ney Music During the Non-Stress Test on Maternal State Anxiety, Autonomic Regulation, and Fetal Reactivity: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07452861
Enrollment
126
Registered
2026-03-05
Start date
2024-05-30
Completion date
2024-08-30
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Maternal Anxiety, Stress

Keywords

non-stress test, music intervention, maternal anxiety, autonomic regulation, fetal reactivity, ney music

Brief summary

This randomized controlled trial evaluates the effects of listening to ney music during routine non-stress testing (NST) on maternal psychological and physiological responses and fetal reactivity. Maternal anxiety during NST may activate sympathetic pathways and potentially influence fetal heart rate patterns. A total of 126 pregnant women at ≥32 weeks' gestation were randomly assigned to either an intervention group (ney music during NST) or a control group (standard NST care). Maternal state anxiety (State-Trait Anxiety Inventory-State), perceived stress and anxiety (DASS-21), blood pressure, heart rate, respiratory rate, oxygen saturation, and NST reactivity were assessed before and after the procedure. The primary objective is to determine whether ney music reduces acute maternal state anxiety during NST. Secondary objectives include evaluating its effects on autonomic physiological parameters and fetal NST reactivity.

Interventions

BEHAVIORALNey Music

Listening to prerecorded ney music through headphones during the 20-minute NST procedure.

Sponsors

Hediye Karakoç
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

were: * age ≥18 years, * gestational age ≥32 weeks, * singleton pregnancy, * absence of known fetal cardiovascular anomalies, * no visual or hearing impairments, * having eaten at least two hours before the NST, * bladder emptied prior to the procedure, * voluntary participation.

Exclusion criteria

included: * pre-existing maternal medical conditions (hypertension, diabetes, obesity), * multiple pregnancy, * smoking, * known fetal abnormalities or fetal distress, * inherited anemia or sexually transmitted infections.

Design outcomes

Primary

MeasureTime frameDescription
State Anxiety (STAI-S Score)Immediately before NST and immediately after NST (20 minutes)Change in maternal state anxiety measured using the State-Trait Anxiety Inventory-State (STAI-S) before and immediately after the non-stress test (NST).

Secondary

MeasureTime frame
Systolic Blood Pressure (mmHg)Before and immediately after NST (20 minutes)
Diastolic Blood Pressure (mmHg)Before and immediately after NST (20 minutes)
Heart Rate (beats per minute)Before and immediately after NST (20 minutes)
Respiratory Rate (breaths per minute)Before and immediately after NST (20 minutes)
Oxygen Saturation (%)Before and immediately after NST (20 minutes)
NST Reactivity (Reactive vs Non-reactive)During 20-minute NST session

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026