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
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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NOT_YET_RECRUITING
NA
146 participants
INTERVENTIONAL
2024-10-01
2025-04-30
Brief Summary
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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
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Acupressure group
Acupressure will be applied to the experimental group before suturing.
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.
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.
control group
No intervention will be made to the control group. Routine emergency room practice will be carried out.
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.
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.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
18 Years
ALL
Yes
Sponsors
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Ezgi BOLAT
OTHER
Responsible Party
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Ezgi BOLAT
graduate student
Central Contacts
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Other Identifiers
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MU-EBOLAT-804
Identifier Type: -
Identifier Source: org_study_id
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