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CompletedNCT06486701singingUpdated Jul 3, 2024

Effect of Singing in Abdominal Surgery Patients

An interventional study of have a sing in Abdominal Pain and Anxiety, sponsored by Istanbul Aydın University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2024-07-03.

Sponsored by Istanbul Aydın University · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Jan 2024, registered May 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Abdominal Pain
  • Anxiety

Keywords

  • Signign
  • Anxiety
  • Pain
  • Vital signs
  • Abdominal surgery patients
03

In context

Abdominal Pain

338 studies on the registry are indexed under Abdominal Pain; 55 are open to participants now.

This study's enrollment of 60 is below the median of 72 across 250 interventional studies indexed under Abdominal Pain.

Browse Abdominal Pain studies →

Lead sponsor

Istanbul Aydın University is the lead sponsor of 65 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Abdominal surgery patiens
  • 18 and more than age

Exclusion criteria

Exclusion Criteria:

  • No abdominal surgery patients
  • under 18 age
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Experimental

    Singing

    Behavioral: have a sing

  • No intervention
    No intervention

    Control

Interventions

  • Behavioralhave a sing

    Singing

    Also known as: Singing

06

What researchers measure

Primary outcomes

  1. Vital signs, pain and anxiety: Measurement will be made with the Vital signs, pain and anxiety

    It will be measure to sing a song after Abdominal Surgery

    Time frame: total of six month

Secondary outcomes

  1. Vital signs, pain and anxiety: Measurement will be made with the Vital signs, pain and Anxiety

    No intervention, the control group abdominal surgery patients

    Time frame: total of six month

07

Study locations

1 site
  • Medicana Kadikoy Hospital
    Istanbul, 34697, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06486701
Lead sponsor
Istanbul Aydın University
Responsible party
SEMRA BÜLBÜLOĞLU (Clinical Assoc. Professor, Istanbul Aydın University) — Principal investigator
First posted
Jul 3, 2024
Start date
Jan 1, 2024
Primary completion
Feb 1, 2024
Completion
Feb 9, 2024
Last update
Jul 3, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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