RECRUITING

Music Use in Parturients Admitted to Labor & Delivery

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to learn if music use affects anxiety or pain levels in parturients admitted to labor and delivery. It will also learn about the effect of music use on patient satisfaction. The main questions it aims to answer are: Does music use affect anxiety levels in parturients admitted to labor and delivery? Does music use affect pain levels in parturients admitted to labor and delivery? Does music use affect patient satisfaction in parturients admitted to labor and delivery? Researchers will compare music to a control (no music) to see if music affects anxiety levels in parturients admitted to labor and delivery. Participants will: Listen to music or listen to no music for a 10 minute duration in the labor and delivery unit. Answer questions about anxiety and pain levels at a few different timepoints. Have information collected from medical charts (vital signs and cervical dilation). Rate their satisfaction with care.

Official Title

A Randomized Controlled Trial of Music Use in Parturients Admitted to Labor & Delivery

Quick Facts

Study Start:2025-05-30
Study Completion:2026-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06969105

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age: 18 years or older
  2. * Laboring parturients or those scheduled for an induction of labor
  3. * Able to provide informed consent
  4. * American Society of Anesthesiologists (ASA) physical status rating of II-III
  1. * Patient refusal
  2. * Impaired hearing
  3. * Patient is taking at least one anxiolytic medication daily at baseline
  4. * Intrauterine fetal demise
  5. * Severe psychiatric disorder

Contacts and Locations

Study Contact

Sophia Struzziero, Medical Student
CONTACT
6178331209
sophia.struzziero@tufts.edu

Study Locations (Sites)

Tufts Medical Center
Boston, Massachusetts, 02111
United States

Collaborators and Investigators

Sponsor: Tufts Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-30
Study Completion Date2026-05

Study Record Updates

Study Start Date2025-05-30
Study Completion Date2026-05

Terms related to this study

Keywords Provided by Researchers

  • music
  • labor and delivery
  • parturients
  • anxiety
  • analgesia
  • anesthesia
  • pain
  • epidural

Additional Relevant MeSH Terms

  • Anxiety
  • Pain
  • Patient Satisfaction