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THE EFFECT OF RELAXATION EXERCİSE ON COMFORT AND ANXIETY IN HERNIATED LUMBAR DISC SURGERY

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06688773
Enrollment
42
Registered
2024-11-14
Start date
2023-03-01
Completion date
2023-07-15
Last updated
2024-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar Disc Herniation

Keywords

Anxiety, comfort level, nursing, lumbar disc herniation, progressive relaxation exercises

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.

Interventions

BEHAVIORALProgressive relaxation exercise

In this study, the relaxation exercises CD, which is a material created by the Turkish Psychological Association, was used. This CD consists of three parts. The first part consists of 10 minutes and this part explains the definition and purpose of deep relaxation exercise and the points to be considered during the exercise. The second part of the CD consists of 30 minutes of verbal explanation of the items of relaxation exercises accompanied by the sound of a stream. The third part consists of 30 minutes and includes only relaxation music.

OTHERControl group: Standart nursing care group

Routine postoperative patient care in the clinic was applied.

Sponsors

Bandırma Onyedi Eylül University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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,

Design outcomes

Primary

MeasureTime frameDescription
ComfortComfort 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.
Anxietypostoperative day 1 before patients are mobilisedMeasured 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026