The Effect of Acupressure Applied Before Suturing Procedure in the Emergency Department on Anxiety and Vital Signs

NCT ID: NCT06636903

Last Updated: 2024-10-15

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

146 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-01

Study Completion Date

2025-04-30

Brief Summary

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This study suggests that the anxiety experienced by patients during suturing in the emergency department can be reduced with acupressure and offers a research proposal on vital signs.

Problem: During suturing in the emergency department, patients experience high levels of anxiety due to the pain they experience and fear of the procedure. This situation complicates the treatment process, negatively affects the health of patients and creates a difficult situation for healthcare professionals.

Solution Suggestion: Acupressure can be used as a non-invasive, safe and effective method to reduce patients\' anxiety. Acupressure reduces pain, provides relaxation and reduces anxiety by increasing the secretion of endorphins in the body.

Purpose of the Study: The purpose of this study is to evaluate the effects of applying acupressure to patients before suturing in the emergency department on their anxiety levels and vital signs (such as blood pressure, heart rate).

In summary, this research has a significant potential that emergency room nurses can improve patients\' quality of life and make treatment processes more effective by using acupressure in patient care.

Key Words: Acupressure, Suturing, Anxiety, Vital Signs, Emergency Department

Detailed Description

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Conditions

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Anxiety Vital Signs

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized parallel controlled experimental study design
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants
A biostatistician who is not involved in the study will be randomly assigned to groups A and B created by a biostatistician in a computer environment. As a result of the drawing of lots, whether groups A and B will be the study or control group will be determined by tossing a coin at the beginning of the study. Information indicating that the patients included in the study sample were assigned to groups A and B according to the randomization table will be placed in an opaque envelope. This envelope will be kept by the coordinator researcher (GAU) and when the researcher (EB) goes to the patient for the application, he will open the envelope after filling out the \"Informed Consent Form\" and learn which group the patient is in.

Study Groups

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Acupressure group

Acupressure will be applied to the experimental group before suturing.

Group Type EXPERIMENTAL

Acupressure

Intervention Type OTHER

Before pressing directly on the point for acupressure, a gentle warming, relaxing and preparatory process of approximately 15 seconds should be performed on the point area. In this case, manual pressure with the thumb, index finger and/or middle finger will be applied sequentially (in the rhythm of breathing) without lifting the finger for an average of 1.5 minutes on each point, at a frequency that does not disturb the person, does not cause pain and has a calming effect. Before the suturing procedure, acupressure will be applied to the HT7 and Li4 points by a researcher (EB) who has an acupressure certificate.

Acupressure

Intervention Type OTHER

Before and after acupressure, vital signs and before acupressure, anxiety scores will be checked using the Spielger State Anxiety Scale. In addition, vital signs and anxiety scores will be checked again immediately after the stitching procedure.

control group

No intervention will be made to the control group. Routine emergency room practice will be carried out.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Acupressure

Before pressing directly on the point for acupressure, a gentle warming, relaxing and preparatory process of approximately 15 seconds should be performed on the point area. In this case, manual pressure with the thumb, index finger and/or middle finger will be applied sequentially (in the rhythm of breathing) without lifting the finger for an average of 1.5 minutes on each point, at a frequency that does not disturb the person, does not cause pain and has a calming effect. Before the suturing procedure, acupressure will be applied to the HT7 and Li4 points by a researcher (EB) who has an acupressure certificate.

Intervention Type OTHER

Acupressure

Before and after acupressure, vital signs and before acupressure, anxiety scores will be checked using the Spielger State Anxiety Scale. In addition, vital signs and anxiety scores will be checked again immediately after the stitching procedure.

Intervention Type OTHER

Other Intervention Names

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Acupressure Group

Eligibility Criteria

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Inclusion Criteria

* Suturing is done with local anesthesia,
* Those who are 18 years or older,
* Conscious, oriented and cooperative,
* Able to read and understand Turkish,
* Agreeing to participate in the study,
* Anxiety not diagnosed,
* Not using medication for anxiety,
* No acupressure experience,
* No physical problems that would prevent acupressure application to Ht7 and Li4 points,
* Not pregnant,
* Patients who sign the \"Voluntary Informed Consent Form\" will be included.

Exclusion Criteria

* Those who are under 18 years of age,
* Unconscious, unoriented and uncooperative,
* Cannot read and understand Turkish,
* Those who do not agree to participate in the study,
* -Diagnosed with anxiety,
* -Using medication for anxiety (anxiolytic, antidepressant, antipsychotic, etc.),
* Having previous acupressure experience,
* Having a physical problem that prevents the application of acupressure to Ht7 and Li4 points,
* Pregnant,
* Patients who do not sign the \"Voluntary Informed Consent Form\" will not be included.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ezgi BOLAT

OTHER

Sponsor Role lead

Responsible Party

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Ezgi BOLAT

graduate student

Responsibility Role SPONSOR_INVESTIGATOR

Central Contacts

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Ezgi Bolat, Master

Role: CONTACT

+90-538-055-8567

Other Identifiers

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MU-EBOLAT-804

Identifier Type: -

Identifier Source: org_study_id

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