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Patient Satisfaction During Cesarean Delivery

Patient Satisfaction of the Environment During Cesarean Delivery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06539754
Enrollment
61
Registered
2024-08-06
Start date
2024-11-25
Completion date
2025-11-10
Last updated
2025-11-12

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

Conditions

Patient Satisfaction

Keywords

Cesarean delivery

Brief summary

The goal of this interventional study is to determine whether the option to listen to music during cesarean delivery increases the participants satisfaction. Participants and their support person will be asked to fill out a short survey and mark their satisfaction on a visual analog scale. Vital signs will be recorded during their procedure.

Detailed description

Currently, our institution does not routinely offer music during cesarean delivery. The goal of this study would be to determine whether the option to listen to music improves patient satisfaction. Also, the study would examine support person satisfaction and changes in maternal vital signs from prior to entering the operating room as compared to prior to exiting the operating room in a sample of patients. If positive satisfaction results are noted in those randomized to the music arm, this would be a low-cost intervention that providers could utilize to increase patient satisfaction during surgery. This will be a prospective randomized controlled trial to determine whether the option of music being played in the operating room can impact the experience for the patient. Subjects will be randomized via central computer-generated randomization 1:1 to either have music played during their procedure or no music played during their procedure. A per protocol analysis will be performed.

Interventions

BEHAVIORALMusic

Participants will have bone conducting headphones available to listen to the music of their choice from premade Spotify playlists.

Sponsors

Geisinger Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Masking description

Participants will be randomized in 1:1 stratification to receive music during their procedure or not. Participants will not be aware of the intervention. If a patient is randomized into music, they will be offered headphones to listen to during their procedure.

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Singleton pregnancy * Second or third cesarean delivery * Scheduled cesarean delivery at Geisinger Medical Center * Able and willing to provide consent * English speaking * Greater than or equal to 37 weeks' gestation

Exclusion criteria

* Fetal anomaly * Multifetal gestation * Hearing loss requiring a sign interpreter or hearing aids * Planned general anesthesia * Intrauterine fetal demise * Participants that present in labor or require urgent/emergent cesarean delivery

Design outcomes

Primary

MeasureTime frameDescription
Participant satisfactionThis is collected during the study duration, on average 6 hours.Visual analog scales from 0-10 (0=extremely unsatisfied, 10=extremely satisfied) will be collected by the patient marking on the line prior to the procedure and during skin closure.

Secondary

MeasureTime frameDescription
Support person satisfactionThis is collected through the duration of the study, on average 6 hours,Visual analog scales from 0-10 (0=extremely unsatisfied, 10=extremely satisfied) will be collected by the support person marking on a line during the participant's skin closure.
Heart rateThis will be collected during the study duration, an average 6 hours.Participants heart rate will be recorded at the time of consent and during skin closure.
Music and satisfactionThis is collected during the study duration, on average 6 hours.Patient's will be asked after their procedure whether they believe music did or would have improved their satisfaction during cesarean delivery using a visual analog scale (0-10)
Blood pressureThis will be collected during the study duration, an average 6 hours.Participants blood pressure (systolic and diastolic) will be recorded at the time of consent and during skin closure.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026