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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03816501
Other study ID # Anxiety
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2019
Est. completion date May 15, 2019

Study information

Verified date September 2019
Source Ankara Diskapi Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, we are planning to evaluate whether listening to the music of the patient's choice preoperatively contributes to postoperative anxiety.


Description:

Preoperative anxiety can be detected via structured and standardised screening by the State - Trait Anxiety Inventory (STAI) I and II.

117 patients scheduled for inguinal hernia surgery for any reason in the age range of 18-70 will be included in our study. preoperative STAI I and II score (anxiety questionnaire) will be applied to each patient. The patients will be divided into two groups as preoperative music played and not played. The list of patients listening to the music will be played through the headphones which are the preference of the patients. The postoperative STAI questionnaire will be applied again. results will be evaluated statistically


Recruitment information / eligibility

Status Completed
Enrollment 117
Est. completion date May 15, 2019
Est. primary completion date May 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- inguinal hernia surgery

- speak Turkish language

Exclusion Criteria:

- Patients with dementia and psychiatric disorders

- anxiolytic and psychiatric drug users

- patients without written consent

- poor vision,

- significant hearing loss,

- active opioid use,

- unwillingness to participate in the study

- unwillingness to listening to music

Study Design


Related Conditions & MeSH terms


Intervention

Other:
music
The preference of the patients will be listened to preoperatively through the headphones
no music
the patients will not be listened

Locations

Country Name City State
Turkey Diskapi Teaching and Research Hospital Ankara Altindag

Sponsors (1)

Lead Sponsor Collaborator
Ankara Diskapi Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary STAI score preoperative and postoperative STAI I and II score questions will be asked. 24 hours
Primary 11-point numerical rating scale (NRS) 11-point numerical rating scale for pain (0='no pain' and 10='worst pain possible pain') were explained. 24 hours