Osmaniye State Hospital" (OSH)

July 15, 2024 updated by: Songul Gungor, Osmaniye Korkut Ata University

Effect of Progressive Relaxations Applied After Laparoscopic Cholecystectomy on Pain, Nausea and Vomiting

Objective: It was conducted as a randomized controlled experimental study to determine the effect of progressive relaxation exercise applied after laparoscopic cholecystectomy on postoperative pain, nausea and vomiting. Method: The population of the study consisted of 105 patients who underwent elective planned laparoscopic cholecystectomy at Osmaniye State Hospital General Surgery Clinic between 25 May and 25 August 2023(Study=38, Control=38). 76 patients, who constituted the sample of the study, were assigned to the study and control groups. Data were collected using the Patient Introduction Form Visual Comparison Scale and Perioperative Patient Monitoring Form.

Patients in the study group underwent progressive relaxation exercises at the 2nd, 6th, 12th and 24th hours after surgery. Frequency, average, Chi-Square test, Independent t-test and Repeated Measures ANOVA test were used to evaluate the data. Results: When the comparison between groups is examined; It was determined that the average pain intensity scores of the patients in the study group at the 6th, 12th and 24th postoperative hours decreased more than the control group and the difference between them was statistically significant (p<0.05). When the comparison between groups is examined; It was determined that the average nausea severity scores of the patients in the study group at the 6th, 12th and 24th postoperative hours decreased significantly compared to the control group and the difference between them was statistically significant (p<0.05). It was determined that there was a decrease in vomiting rates in the study group compared to the control group at the 6th and 12th hours after surgery and the difference between them was significant. Conclusion and Recommendations: It has been determined that progressive relaxation exercises reduces pain, nausea and vomiting after laparoscopic cholecystectomy. In line with the results obtained from the research, it is recommended that nurses teach progressive relaxation exercises to patients and encourage their use, as they are easy to apply to patients and are not an invasive method. Keywords: Laparoscopic cholecystectomy, nausea, nurse, pain, progressive relaxation exercises.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Data were collected at Osmaniye State Hospital General Surgery Clinic between 25 May and 25 August 2023.

Among 76 patients who were hospitalized for laparoscopic cholecystectomy and volunteered to participate in the study (Study group = 38, Control group = 38) was taken. Before starting the application, ;Informed Voluntary ; was obtained from the patients.

Verbal and written permissions were obtained by reading the ; (Annex-I). Working group - Before the patient undergoes surgery, the Patient Information Form (Annex-II) information is obtained from the patient file and asked to the patient.

has been filled.

  • The researcher was informed about the surgical intervention, expected nausea and vomiting, and pain.
  • The first 10-minute part of the CD audio recordings prepared by the Turkish Psychologists Association is about deep relaxation.

purpose; The second 30-minute part includes instructions for relaxation exercises; The last 30 minutes are just it consists of relaxation music.

- In addition to standard treatment and care for laparoscopic cholecystectomy, volunteers who accept the study Progressive relaxation exercises were applied by the researcher at the 2nd, 6th, 12th and 24th hours after surgery.

When the literature review on PGE was made, it was seen that the application time and frequency of these exercises were not standard; 6th, 12th, 24th hours after surgery; It was applied on the 2nd day after surgery and the total number of sessions varied.

It is seen to show . In our study, PGE was detected at the 2nd, 6th, 12th and 24th hours after surgery.

has been implemented.Control group patients were informed about the research and received Informed Voluntary Consent Form (ANNEX-I) verbal and written permissions were obtained. - Before the surgery, the Patient Introduction Form (Annex-II) was checked both from the file and received verbal confirmation from the patient.

was filled in.

  • The researcher was informed about the surgical intervention, expected nausea and vomiting, and pain.
  • Patients in the control group were given the standard procedure for laparoscopic cholecystectomy only during the research period.

treatment and care were applied.

- No postoperative intervention was performed on the control group, and the researcher did not perform surgery after surgery.

Visual Comparison Scale (ANNEX-III) form for the severity of pain, nausea and vomiting at the 2nd, 6th, 12th and 24th hours The patient is asked to mark it with a pen or verbally indicate the severity between 1 and 10 on the form.

marking has been made.

  • After the postoperative pain, nausea and vomiting status is determined on the Visual Comparison Scale, perioperative Patient Follow-up Form (ANNEX-IV) has been filled out.
  • Data collection process of the research in order to eliminate ethical problems that may occur in the control group After completion, these patients were trained in progressive relaxation exercises.

Study Type

Interventional

Enrollment (Actual)

76

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

    • Osmani̇ye
      • Merkez, Osmani̇ye, Turkey, 80010
        • Osmaniye State Hospital

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • *To participate in the research willing

    • Prevents exercise creating a chronic without disease (COPD, heart failure etc.)
    • Hearing problem not found
    • At least primary school graduate the one which...
    • A psychiatric diagnosis non-major depression, anxiety disorders etc.) and anxiety or a drug for depression non-user
    • Elective laparoscopic having a cholecystectomy
    • Oriented to person, place and time the one which...
    • American Anesthesia Association(ASA) classification I, II or III the one which...

Exclusion Criteria:

Under 18 and over 70 patients over (n=2)

  • Agree to participate in the research not (n=12)
  • Patients undergoing emergency surgery
  • Prevents exercise with disease causing
  • Hearing problem found
  • Having a psychiatric diagnosis (major depression, anxiety disorders etc.) and anxiety or a depression taking medication
  • Pregnant
  • Suffering from motion sickness
  • Lack of cooperation
  • Basic during surgery in life functions developing complications
  • Open cholecystectomy (n=2)
  • American Society of Anesthesiologists (ASA) classification IV are(n=7)
  • Previous PGE exercises educated

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Group 1

Patients in the control group were given only the standard procedure for laparoscopic cholecystectomy during the research period.

treatment and care were applied.

Experimental: Group 2
The first 10-minute part of the CD audio recordings prepared by the Turkish Psychologists Association is about deep relaxation. purpose; The second 30-minute part includes instructions for relaxation exercises; The last 30 minutes are just It consists of relaxation music[145]. In our study, the instructions in the second part were used. - In addition to standard treatment and care for laparoscopic cholecystectomy, volunteers who accept the study Progressive relaxation exercises were applied by the researcher at the 2nd, 6th, 12th and 24th hours after surgery. When the literature review on PGE was made, it was seen that the application time and frequency of these exercises were not standard; 6th, 12th, 24th hours after surgery; It was applied on the 2nd day after surgery and the total number of sessions varied. It is seen to show. In our study, PGE was detected at the 2nd, 6t

The first 10-minute part of the CD audio recordings prepared by the Turkish Psychologists Association is about deep relaxation.

purpose; The second 30-minute part includes instructions for relaxation exercises; The last 30 minutes are just consists of relaxation music

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
pain, nausea and vomiting 1
Time Frame: at the 2nd hour after surgery
The severity of pain, nausea, and vomiting was assessed by the researcher at the 2nd hour using a visual analog scale.
at the 2nd hour after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
pain, nausea and vomiting 2
Time Frame: at the 6nd hours after surgery
he severity of pain, nausea, and vomiting was assessed by the researcher at the 6th hour using a visual analog scale. vomiting at the 6th hours after surgery.
at the 6nd hours after surgery
pain, nausea and vomiting 3
Time Frame: at the 12th hour after surgery
The severity of pain, nausea, and vomiting was assessed by the researcher at the 12 thhour using a visual analog scale.
at the 12th hour after surgery
pain, nausea and vomiting 4
Time Frame: at the 24th hour after surgery
The severity of pain, nausea, and vomiting was assessed by the researcher at the 24th hour using a visual analog scale.
at the 24th hour after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Didem LAFÇI, associate professor, Mersin University

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)

May 25, 2023

Primary Completion (Actual)

August 25, 2023

Study Completion (Actual)

August 25, 2023

Study Registration Dates

First Submitted

May 28, 2024

First Submitted That Met QC Criteria

July 15, 2024

First Posted (Actual)

July 19, 2024

Study Record Updates

Last Update Posted (Actual)

July 19, 2024

Last Update Submitted That Met QC Criteria

July 15, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Osmaniye State Hospital"

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

no ipd

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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.

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