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Clinical Trials/NCT06688773
NCT06688773
Completed
N/A

THE EFFECT OF PROGRESSIVE RELAXATION EXERCISES ON COMFORT AND ANXIETY LEVEL OF PATIENTS WITH LUMBAR DISC HERNIATION SURGERY: CLINICAL TRIAL

Bandırma Onyedi Eylül University1 site in 1 country42 target enrollmentMarch 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Lumbar Disc Herniation
Sponsor
Bandırma Onyedi Eylül University
Enrollment
42
Locations
1
Primary Endpoint
Comfort
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study aimed to investigate the effect of progressive relaxation exercises on the comfort and anxiety levels of patients undergoing lumbar disc herniation surgery in the neurosurgery clinic.

Detailed Description

This study aimed to investigate the effect of progressive relaxation exercises on the comfort and anxiety levels of patients undergoing lumbar disc herniation surgery in the neurosurgery clinic.The study's data was conducted as experimental study on patients who will undergo surgery in the neurosurgery clinic of the Ministry of Health Muammer Ağım Gemlik State Hospital between March 2023 and July 2023. The sociodemographic Characteristics Questionnaire, Immobilisation Comfort Scale and State Anxiety Scale were used for data collection. The Shapiro-Wilk normality test, the t-test for the same and different groups mean and standard deviation, Pearson correlation analysis were used to evaluate the data.

Registry
clinicaltrials.gov
Start Date
March 1, 2023
End Date
July 15, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Bandırma Onyedi Eylül University
Responsible Party
Principal Investigator
Principal Investigator

Didem Ayhan

Associate Professor

Bandırma Onyedi Eylül University

Eligibility Criteria

Inclusion Criteria

  • Over 18 years of age, elective surgery,
  • Undergoing LDH surgery for the first time,
  • Undergoing lumbarmicrodiscectomy surgery,
  • ASA 1 and 2 classification,
  • Receiving only general anaesthesia under endotracheal intubation,
  • Without cognitive impairment, hearing and vision problems,
  • Volunteered to participate in the study,
  • Patients who did not develop any complications that would affect comfort and anxiety

Exclusion Criteria

  • 18 years of age or younger,
  • With psychiatric disorders,

Outcomes

Primary Outcomes

Comfort

Time Frame: Comfort levels of the patients were measured on the morning of the first postoperative day (before mobilisation)

Measured using the "Immobilisation Comfort Scale". The total scores obtained from the scale vary between 20 and 120, and a high score indicates that the comfort is good.

Anxiety

Time Frame: postoperative day 1 before patients are mobilised

Measured with "State Anxiety Scale". The state anxiety section of the state trait anxiety scale was used. In the evaluation of the scale, all items are summed and this score is subtracted from the sum of the items marked as reversed and the number 50 is added to the result. The result is the state anxiety score. The total score that can be obtained from the scale is minimum 20 and maximum 80. The increase in the score in this range indicates that the anxiety level of the individual increases.

Study Sites (1)

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