Music for Anxiety Management in Cesarean Delivery

NCT ID: NCT06496932

Last Updated: 2024-07-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-01

Study Completion Date

2024-02-15

Brief Summary

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A randomized controlled trial will be conducted to determine examine the effects of music played during cesarean delivery on maternal anxiety and vital signs.

Detailed Description

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It will tested the hypotheses that there is no difference between the intervention and control groups of pregnant women after the intervention in terms of anxiety and vita lsymptoms.

Conditions

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Pregnancy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Listen to music group

The study group will be played music during the cesarean section.

Group Type EXPERIMENTAL

Listen to music

Intervention Type OTHER

Women in the intervention groups will listen to nature and bird sounds through over-the-ear headphones after spinal anesthesia for cesarean section until the suturing is completed.

Standart cesarean procedure

The control group continued to receive the routine care

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Listen to music

Women in the intervention groups will listen to nature and bird sounds through over-the-ear headphones after spinal anesthesia for cesarean section until the suturing is completed.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

\- Aged between 18-35 years,

* Undergoing cesarean section under spinal anesthesia,
* Experiencing spontaneous and singleton pregnancy,
* With a gestational age greater than 37 weeks,
* Pregnant individuals who have had at least 4 routine check-ups during pregnancy conducted by a member of the research team,
* Scheduled for cesarean section (regardless of the number of previous cesarean sections).

Exclusion Criteria

* Having high-risk pregnancies such as preeclampsia, early membrane rupture, and placental abruption, • Being scheduled for emergency cesarean section for any reason
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Aydin Adnan Menderes University

OTHER

Sponsor Role lead

Responsible Party

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Tuğba Dündar

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tuğba Dündar

Role: STUDY_CHAIR

AydınAdnan Menderes University, Faculy of Nursing, Division Public Health Nursing

Locations

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Adnan Menderes University

Aydin, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Interventional trial

Identifier Type: -

Identifier Source: org_study_id

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