NCT06969105 Music Use in Parturients Admitted to Labor & Delivery
| NCT ID | NCT06969105 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Tufts Medical Center |
| Condition | Anxiety |
| Study Type | INTERVENTIONAL |
| Enrollment | 106 participants |
| Start Date | 2025-05-30 |
| Primary Completion | 2027-05 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 106 participants in total. It began in 2025-05-30 with a primary completion date of 2027-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: * Age: 18 years or older * Laboring parturients or those scheduled for an induction of labor * Able to provide informed consent * American Society of Anesthesiologists (ASA) physical status rating of II-III Exclusion Criteria: * Patient refusal * Impaired hearing * Patient is taking at least one anxiolytic medication daily at baseline * Intrauterine fetal demise * Severe psychiatric disorder
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06969105 clinical trial?
This trial is open to female participants only, aged 18 Years or older, studying Anxiety. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06969105 currently recruiting?
Yes, NCT06969105 is actively recruiting participants. Contact the research team at sophia.struzziero@tufts.edu for enrollment information.
Where is the NCT06969105 trial being conducted?
This trial is being conducted at Boston, United States.
Who is sponsoring the NCT06969105 clinical trial?
NCT06969105 is sponsored by Tufts Medical Center. The trial plans to enroll 106 participants.
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