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Music Listening During NST Monitoring

Effects of Music Listening During Non-Stress Test Monitoring on Fetal Parameters, Maternal Anxiety, Loneliness, and Positive-Negative Affect: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07414641
Enrollment
100
Registered
2026-02-17
Start date
2023-01-01
Completion date
2023-04-30
Last updated
2026-02-17

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

Conditions

Fetal Well-Being, Maternal Anxiety, Pregnancy

Brief summary

This study evaluated whether listening to music during routine non-stress test (NST) monitoring affects fetal parameters and maternal psychological outcomes. NST is a common prenatal assessment, and some pregnant women may experience anxiety or negative emotions during the procedure. Music listening is a non-pharmacological approach that may improve emotional well-being and potentially influence fetal responses. In this randomized controlled trial, pregnant women who attended an NST unit were assigned either to a music group that listened to music through headphones during NST monitoring or to a control group that received routine NST monitoring without music. Fetal parameters were assessed from NST recordings. Maternal anxiety, loneliness, and positive-negative affect were measured before and after the NST using validated questionnaires. The results of this study aim to inform supportive prenatal care practices and evaluate whether music listening can be used as a simple intervention during NST monitoring.

Interventions

BEHAVIORALMusic Listening During NST

Participants listened to music through headphones during routine NST monitoring in a left lateral position for at least 20 minutes. The volume was adjusted according to participant preference.

Sponsors

Biruni University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women attending the NST unit during the study period * Aged 18 years or older * Volunteered to participate and provided written informed consent

Exclusion criteria

* Inability to read and write Turkish * Hearing impairment or mental health conditions limiting participation * Multiple pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Maternal State AnxietyBaseline (pre-NST) and immediately post-NST (same visit)Change in maternal anxiety measured using the State-Trait Anxiety Inventory - State Form (STAI-S). Scores range from 20 to 80; higher scores indicate greater anxiety.

Secondary

MeasureTime frameDescription
Loneliness (Social and Emotional Loneliness)Baseline (pre-NST) and immediately post-NST (same visit)Change in loneliness measured using the Social and Emotional Loneliness Scale for Adults - Short Form (SELSA-S). Total scores range from 15 to 105; higher scores indicate greater loneliness.
Positive and Negative AffectBaseline (pre-NST) and immediately post-NST (same visit)Change in affect measured using the Positive and Negative Affect Schedule (PANAS). Each subscale ranges from 10 to 50; higher positive scores indicate more positive affect and higher negative scores indicate greater negative affect.
Fetal Heart Rate During NSTDuring NST monitoring (same visit)Fetal heart rate assessed from NST recordings during the monitoring session. Measured in beats per minute; normal patterns (120-140/min) indicate better fetal well-being.
Fetal Movement Count During NSTDuring NST monitoring (same visit).Number of fetal movements recorded by the mother using the event marker during NST monitoring. Higher counts indicate greater fetal activity.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORNİLGUN AVCI

Biruni University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026