The Effect of Mobilising Patients Using Nature Sounds on Anxiety, Pain and Stress Levels (After Laparosc)
May 4, 2026 updated by: Seda Cansu Yeniğün, Akdeniz University
The Effect of Mobilising Patients Using Nature Sounds on Anxiety, Pain and Stress Levels of Patients After Laparoscopic Cholecystectomy Surgery
The Effect of Mobilization Using Nature Sounds on Patients' Anxiety, Pain and Stress Levels
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
70
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Kumluca
-
Antalya, Kumluca, Turkey (Türkiye), 07350
- Kumluca State Hospital
-
-
Merkez
-
Edirne, Merkez, Turkey (Türkiye), 22030
- Trakya University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Individuals who are willing to participate in the study,
- Patients undergoing their first laparoscopic surgery due to gallbladder stones,
- Patients scheduled for elective surgical procedures,
- Patients with no hearing impairment,
- Patients with no vision impairment,
- Mentally stable individuals,
- Individuals who are open to communication and cooperation,
- Patients aged 18 years and older will be included in the study.
Exclusion Criteria:
- Individuals with mental health issues,
- Individuals who are unwilling to participate,
- Patients with hearing impairment,
- Patients undergoing their second surgery (recurrent) due to gallbladder stones,
- Patients using hearing aids,
- Individuals who are uncooperative or unwilling to communicate,
- Patients who require emergency surgery will not be included in the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
The standard care protocol of the service will be applied to the patients in the control group.
The patients will be mobilized.(
|
|
|
Experimental: Intervention Group
Patients in this group will be mobilized and will be played nature-based sounds through headphones.
|
After a 50-meter walk while listening to the sounds of nature, the patient will walk 50 meters again to his/her room and then to his/her bed, where he/she will be seated.
Then, the researcher nurse will remove the headphones from the patient's ears and ensure that the patient rests in a comfortable position.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anxiety
Time Frame: Before mobilization 5 minutes and after mobilization 10 minutes
|
Anxiety level will be measured withVirtual Analog Scale-Anxiety (The lowest score is set as 0, and the highest score is set as 10.)
|
Before mobilization 5 minutes and after mobilization 10 minutes
|
|
Stress
Time Frame: before mobilization 5 minutes and after mobilization 10 minutes
|
with smart watch
|
before mobilization 5 minutes and after mobilization 10 minutes
|
|
Pain level
Time Frame: before mobilization 5 minutes and after mobilization 10 minutes
|
Pain level will be measured with Virtual Analog Scale (The lowest score is set as 0, and the highest score is set as 10.)
|
before mobilization 5 minutes and after mobilization 10 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress, pulse, saturation levels
Time Frame: After mobilization 10 minutes
|
with smart watch
|
After mobilization 10 minutes
|
|
After Mobilization Pain Value
Time Frame: After mobilization 10 minutes
|
Virtual Analog Scale (The lowest score is set as 0, and the highest score is set as 10.)
|
After mobilization 10 minutes
|
|
Anxiety
Time Frame: After mobilization 10 minutes
|
Virtual Analog Scale-Anxiety (The lowest score is set as 0, and the highest score is set as 10.)
|
After mobilization 10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 2, 2025
Primary Completion (Actual)
December 1, 2025
Study Completion (Actual)
December 1, 2025
Study Registration Dates
First Submitted
February 22, 2025
First Submitted That Met QC Criteria
February 22, 2025
First Posted (Actual)
February 27, 2025
Study Record Updates
Last Update Posted (Actual)
May 7, 2026
Last Update Submitted That Met QC Criteria
May 4, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Sc129898scy
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.