Effect of Singing in Abdominal Surgery Patients

NCT ID: NCT06486701

Last Updated: 2024-07-03

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

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-01

Study Completion Date

2024-02-09

Brief Summary

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Patients who have undergone abdominal surgery are given a prompt in the postoperative period and asked to sing the song they remember. Vital signs, pain and anxiety levels are measured before and after singing.

Detailed Description

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This study is of a randomized controlled type. Patients who have undergone abdominal surgery are divided into experimental and control groups in the early postoperative period. No intervention is made to the control group by the researchers. Vital signs, pain and anxiety levels are measured half an hour apart as pre-test and post-test.

Patients in the experimental group are given a prompt in the postoperative period and asked to sing the song they remember. Pre-test before singing and post-test after singing, vital signs, pain and anxiety levels are measured. It is expected that singing will calm patients, stabilize their vital signs, and reduce anxiety and pain.

Conditions

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Abdominal Pain Anxiety

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants

Study Groups

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Experimental

Singing

Group Type EXPERIMENTAL

have a sing

Intervention Type BEHAVIORAL

Singing

No intervention

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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have a sing

Singing

Intervention Type BEHAVIORAL

Other Intervention Names

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Singing

Eligibility Criteria

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Inclusion Criteria

* Abdominal surgery patiens
* 18 and more than age

Exclusion Criteria

* No abdominal surgery patients
* under 18 age
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul Aydın University

OTHER

Sponsor Role lead

Responsible Party

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SEMRA BÜLBÜLOĞLU

Clinical Assoc. Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Medicana Kadikoy Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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86.2023fbu

Identifier Type: -

Identifier Source: org_study_id

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