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Efficacy of Music Listening to Shortening Time for Biophysical Profile (RRT)

Q

Queen Savang Vadhana Memorial Hospital, Thailand

Status

Completed

Conditions

Fetal Status, Nonreassuring

Treatments

Diagnostic Test: Trans abdominal ultrasound for assess biophysical profile

Study type

Interventional

Funder types

Other

Identifiers

NCT05729750
004/2565

Details and patient eligibility

About

The goal of this clinical trial is to compare the timeing which assume for assesment of BPP in low risk pregnancy. The main question is the music can be shoetening the timing for BPP? Participants will in study froup will listening the music via headphone before and during the assessment and compre to control gruop which not listening to music during asseeement.

Full description

A single-blind randomized controlled trial conducted from February 2021 to December 2022. The study population consisted of 60 pregnant women with between 18 and 35 years old with gestational age of 32 weeks. An abdominal ultrasound was performed while listening to one song while wearing headphones in the experimental group preceding the biophysical profile assessment. As part of the control group, the same equipment was used and the same assessment protocol was followed, but music was not played during the test.

Enrollment

60 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Single pregnancy (Singleton)
  • Gestational age from 32 weeks onward
  • Pregnant women do not have underlying diseases such as pre-gestational diabetes. high blood pressure
  • No abnormalities in the fetus were found, such as fetal deformities.

Exclusion criteria

  • Pregnant women receiving certain drugs or substances that affect the interpretation of the Biophysical Profile (BPP), e.g., sleeping pills, cigarettes.
  • Pregnant women have hearing problems. or hearing impaired
  • Pregnant women who are unable to wear headphones, e.g., otitis externa - Pregnant women with body mass index greater than 30 kg/m2 prior to pregnancy
  • Uterine contractions were observed during the examination

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

Single Blind

60 participants in 2 patient groups, including a placebo group

Lable litter A (Study group)
Experimental group
Description:
The sealed opaque brown envelope contains a case record form and the letter A paper for listening to the music before and during the BPP assessment (study group), which cannot be visible from the outside.
Treatment:
Diagnostic Test: Trans abdominal ultrasound for assess biophysical profile
Lable litter B (control group)
Placebo Comparator group
Description:
The sealed opaque brown envelope contains a case record form and the letter B for not listening to the music before and during the BPP assessment (control group), which cannot be visible from the outside.
Treatment:
Diagnostic Test: Trans abdominal ultrasound for assess biophysical profile

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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