Directed Imagery Technique Applied to Patients Undergoing Lumbar Disc Herniation Surgery

NCT ID: NCT05283291

Last Updated: 2022-03-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-02-08

Study Completion Date

2022-06-30

Brief Summary

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The Directed Imagery technique (YIT) is a set of stories that people create by first giving relaxation exercises and then visualizing the symbols given by the practitioner. Guided imagery is based on the understanding that the body and mind are interconnected and that the mind can affect the body. In directed imagery, the person's thoughts and imagination are focused and directed to a specific goal by the practitioner, usually through a sound recording. The directed imagery technique can be effective in solving problems such as pain, stress, fatigue, and anxiety in nursing care.

Detailed Description

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1. Patients in the control group; Nursing care will be applied according to the routine care protocol of the clinic where the research was conducted.
2. Patients in the experimental group; In addition to the nursing care given according to the routine care protocol of the clinic where the research was conducted, the "imagery method" will be applied four times in total, once before the operation, once on the 1st day, 2nd day and 3rd day after the operation. It will be ensured that the patients to be imaged are in the supine or semifawler position in a comfortable way and listen to the audio recording with headphones.

Before the application, the patient will be told to listen to the audio recording with headphones at the most convenient time of the day for him, in an environment where he will not be disturbed by others, by putting his phone in airplane mode, after giving advance notice to avoid disturbing family members. Headphones will be provided for each patient by the researcher. In the first meeting, the voice recordings will be transferred to the phones of the individuals via the phone in the Neurosurgery Service. Communication with the patient will be provided in accordance with the pandemic rules. In the preoperative period, "Descriptive Information Form", "Operation-Specific Anxiety Scale", "Richard-Campbell Sleep Scale", "Visual Analog Scale (VAS)", "State Anxiety Scale" will be applied to the experimental and control groups before imagery is performed. After the interventions applied to the experimental group are completed, the scales will be re-administered to the individuals in the experimental and control groups.

Conditions

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Intervertebral Disc Disorder Lumbar With Radiculopathy Surgical or Other Invasive Procedure on Wrong Patient Nurse-Patient Relations

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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İmaginary group

Expert opinion for the scenario will be taken from a psychologist and a psychiatric nurse.

The flow of the script; It will start with breathing exercises and continue with the safe place application, after affirming the functionality that is said while in a safe place in the mind, it will be in the form of waking up by turning to the body and returning to the present.

Headphones will be provided for each patient by the researcher. In the first meeting, the voice recordings will be transferred to the phones of the individuals via the phone in the Neurosurgery Service. Communication with the patient will be provided in accordance with the pandemic rules.

The audio recording will be played twice, in the evening before the operation and on the evening of the operation day.

Group Type EXPERIMENTAL

Directed Imagery Technique

Intervention Type BEHAVIORAL

The sound recording will include a soothing light background music for approximately 30 minutes.

Imagination will be practiced, starting with the patient's focusing his/her attention on his/her breath, relaxation, and relaxation with the suggestions given in the recording with the accompaniment of relaxing music.

Control group

In the routine care applied to the patients, the vitals of the patients are followed, drug treatments are administered and the motor functions of the patients are monitored. In addition, analgesics are routinely administered in the ward for pain and no attempt is made for sleep.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Directed Imagery Technique

The sound recording will include a soothing light background music for approximately 30 minutes.

Imagination will be practiced, starting with the patient's focusing his/her attention on his/her breath, relaxation, and relaxation with the suggestions given in the recording with the accompaniment of relaxing music.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Those who will undergo lumbar disc hernia surgery
2. Compliant with ASA 1 and 2 classification
3. Preoperative hospitalizations
4. Patients without cognitive clouding
5. Patients who can speak Turkish
6. Patients without hearing and vision problems will be included in the study.

Exclusion Criteria

1. Those over the age of eighty or under the age of 18
2. Having a psychiatric disease and using medication
3. Having trouble sleeping and taking medication
4. Those who are classified as ASA 3 and above,
5. Those who have laparoscopic surgery,
6. Those with chronic pain, alcohol, drug and substance addiction,
7. Oncological cases,
8. Those with hearing, vision, speech and cognitive dysfunction,
9. Those who do not speak Turkish,
10. People with high anxiety who use anxiolytics
11. Patients who do not accept the procedure will not be included in the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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TC Erciyes University

OTHER

Sponsor Role lead

Responsible Party

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Eda Albayrak

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Eda Albayrak

Role: PRINCIPAL_INVESTIGATOR

TC Erciyes University

Locations

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Eda Albayrak

Kayseri, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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ErciyesU-Albayrak-001

Identifier Type: -

Identifier Source: org_study_id

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