The Effect of Listening to Surah Al-Inshirah on Pain and Anxiety After Laparoscopic Cholecystectomy Surgery

Sponsor
Seher Tanrıverdi (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06042114
Collaborator
(none)
60
1
2
2
29.9

Study Details

Study Description

Brief Summary

In the postoperative period, good pain and anxiety management is required to minimize complications and ensure recovery. Patients should be evaluated with a holistic approach, taking into account factors such as physical and psychological discomfort, anxiety level, age, gender, previous pain level. Pharmacological and non-pharmacological methods are used to relieve pain and anxiety in the postoperative period.

Non-pharmacological methods reduce the patient's pain and anxiety by creating a feeling of comfort and control in the patient. Relaxation techniques such as hypnosis, yoga and music are among these. The main purpose of these methods is to draw the attention of the individual in another direction. Praying is also one of the non-drug methods, and the number of studies on this subject is very limited, and there are studies where it has been determined that praying and praying reduces the anxiety levels of patients.

Purpose To examine the effect of listening to Surah al-Inshirah on pain and anxiety after laparoscopic cholecystectomy surgery.

Method The population of the study will consist of patients who have undergone laparoscopic cholecystectomy at Mardin Training and Research Hospital and Kızıltepe State Hospital, who meet the inclusion criteria and volunteer to participate in the research.

The study group of 60 people who will participate in the research will be divided into two equal groups according to the table of random numbers obtained from the computer-based Research Randomizer program.

Experimental group patients; A patient descriptive characteristics form will be applied, pretest VAS pain score and state anxiety scale will be applied. Then, the Surah al-Inshirah will be listened to and the final test VAS pain score and state anxiety scale will be applied.

Control group patients; A patient descriptive characteristics form will be applied, pretest VAS pain score and state anxiety scale will be applied. The posttest VAS pain score and state anxiety scale will be applied 10 minutes later, without any intervention.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Surah Inshirah
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Listening to Surah Al-Inshirah on Pain and Anxiety After Laparoscopic Cholecystectomy Surgery
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Listening to Surah Inshirah

Experimental group patients; A patient descriptive characteristics form will be applied, pretest VAS pain score and state anxiety scale will be applied. Then, the Surah al-Inshirah will be listened to and the final test VAS pain score and state anxiety scale will be applied.

Behavioral: Surah Inshirah
Patients in the experimental group will be listened to the Surah al-Inshirah after surgery and its effect on pain and anxiety levels will be evaluated.

No Intervention: control group

Control group patients; A patient descriptive characteristics form will be applied, pretest VAS pain score and state anxiety scale will be applied. The posttest VAS pain score and state anxiety scale will be applied 10 minutes later, without any intervention.

Outcome Measures

Primary Outcome Measures

  1. Patient Information Form [It will be applied to patients in the clinic 2 hours before the laparoscopic cholecystectomy procedure]

    This form, created by the researcher with the support of the relevant literature, consists of 9 questions that question the patients' education level, age, gender, occupation, marital status, income level, previous surgery experience and coping methods used for pain and anxiety in daily life.

Secondary Outcome Measures

  1. Visual Analogue Scale (VAS) [Change from initial Visual Analog Scale in 10 minutes]

    The patient was asked to mark on a 10 cm horizontal line showing his current status on the Visual analog scale. In this study, for pain and anxiety; Markings were made on a 10 cm horizontal line, one end indicating that the patient's pain was very good (0 = no pain), and the other end indicating that the patient's pain was very bad (10 = most severe). The distance from the point where there was no pain or anxiety (0) to the point marked by the patient was measured. The value found shows the patient's pain and anxiety.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients who can be contacted,

  • Patients with an abdominal pain score of 4 and above as evaluated by VAS after laparoscopic cholecystectomy surgery,

  • Patients aged 18 and over were included in the study.

Exclusion Criteria:
  • Patients who can be contacted,

  • Patients with an abdominal pain score of 4 and above as evaluated by VAS after laparoscopic cholecystectomy surgery,

  • Patients aged 18 and over were included in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mardin State Hospital Mardi̇n Turkey

Sponsors and Collaborators

  • Seher Tanrıverdi

Investigators

  • Principal Investigator: SEHET TANRIVERDİ, PhD, Mardin Artuklu University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Seher Tanrıverdi, Asistant Professor, Mardin Artuklu University
ClinicalTrials.gov Identifier:
NCT06042114
Other Study ID Numbers:
  • Mardin-Artuklu University
First Posted:
Sep 18, 2023
Last Update Posted:
Sep 18, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Seher Tanrıverdi, Asistant Professor, Mardin Artuklu University

Study Results

No Results Posted as of Sep 18, 2023