- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06636903
The Effect of Acupressure Applied Before Suturing Procedure in the Emergency Department on Anxiety and Vital Signs
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
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ezgi Bolat, Master
- Phone Number: +90-538-055-8567
- Email: ezgibolat35@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Acupressure group
Acupressure will be applied to the experimental group before suturing.
|
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.
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 Names:
|
|
No Intervention: control group
No intervention will be made to the control group.
Routine emergency room practice will be carried out.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of anxiety before acupressure
Time Frame: before suturing
|
Before the suturing procedure, acupressure will be applied to the Ht7 and Li4 points.The state anxiety scale consists of 20 questions.
The statements in the SAS are evaluated as none 1 point, a little 2 points, a lot 3 points and completely 4 points.
In this section, the statements are divided into direct and reversed.
Reversed statements are: items 1, 2, 5, 8, 10, 11, 15, 16, 19, and 20.
The SAS score is calculated by adding the constant value of 50 to the value obtained by subtracting the total score of the reversed statements from the total score of the direct statements.
The scale score varies between 20-80 and an increase in the score obtained from the scale indicates an increase in the anxiety level.
A total score of 0-19 from the SAS indicates no anxiety, a score of 20-39 indicates mild anxiety, a score of 40-59 indicates moderate anxiety and a score of 60-79 indicates a severe anxiety level.
It is stated that individuals who score above 60 on the SAS need professional help.
|
before suturing
|
|
Evaluation of anxiety after suturing
Time Frame: immediately after suturing
|
Immediately after the stitching, the anxiety scale will be filled out again.
The statements in the SAS are evaluated as none 1 point, a little 2 points, a lot 3 points and completely 4 points.
In this section, the statements are divided into direct and reversed.
Reversed statements are: items 1, 2, 5, 8, 10, 11, 15, 16, 19, and 20.
The SAS score is calculated by adding the constant value of 50 to the value obtained by subtracting the total score of the reversed statements from the total score of the direct statements.
The scale score varies between 20-80 and an increase in the score obtained from the scale indicates an increase in the anxiety level.
A total score of 0-19 from the SAS indicates no anxiety, a score of 20-39 indicates mild anxiety, a score of 40-59 indicates moderate anxiety and a score of 60-79 indicates a severe anxiety level.
It is stated that individuals who score above 60 on the DAS need professional help.
|
immediately after suturing
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of blood pressure before acupressure
Time Frame: Just before acupressure
|
Vital signs will be monitored immediately before acupressure.
The patient's blood pressure will be monitored before acupressure.
The patients' blood pressure will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
Systolic blood pressure of 100-130 mmHg, diastolic blood pressure of 60-80 mmHg.
Normal blood pressure is usually considered to be between 90/60 mmHg and 120/80 mmHg.
|
Just before acupressure
|
|
Assessment of Blood Pressure After Acupressure
Time Frame: After acupressure
|
Vital signs will be monitored immediately after acupressure.
The patient's blood pressure will be monitored after acupressure.
The patients' blood pressure will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
Systolic blood pressure of 100-130 mmHg, diastolic blood pressure of 60-80 mmHg.
Normal blood pressure is usually considered to be between 90/60 mmHg and 120/80 mmHg.
|
After acupressure
|
|
Assesment of blood pressure after suturing
Time Frame: after suturing
|
Vital signs will be monitored immediately after suturing.
The patient's blood pressure will be monitored after suturing.
The patients' blood pressure will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
Systolic blood pressure of 100-130 mmHg, diastolic blood pressure of 60-80 mmHg.
Normal blood pressure is usually considered to be between 90/60 mmHg and 120/80 mmHg.
|
after suturing
|
|
Assesment of heart rate before acupressure
Time Frame: before acupressure
|
Vital signs will be monitored immediately before acupressure.
The patient's heart rate will be monitored before acupressure.
The patient's heart rate will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
A normal heart rate for adults ranges from 60 to 100 beats per minute.
|
before acupressure
|
|
Assesment of heart rate after acupressure
Time Frame: after acupressure
|
Vital signs will be monitored immediately after acupressure.
The patient's heart rate will be monitored after acupressure.
The patient's heart rate will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
A normal heart rate for adults ranges from 60 to 100 beats per minute.
|
after acupressure
|
|
Assesment of heart rate after suturing
Time Frame: after suturing
|
Vital signs will be monitored immediately after suturing.
The patient's heart rate will be monitored after suturing.
The patient's heart rate will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
A normal heart rate for adults ranges from 60 to 100 beats per minute.
|
after suturing
|
|
Assesment of oxygen saturation before acupressure
Time Frame: before acupressure
|
Vital signs will be monitored immediately before acupressure.
The patient's heart rate will be monitored before acupressure.
The patient's heart rate will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
For most people, a normal pulse oximeter reading for your oxygen saturation level is between 95% and 100%.
|
before acupressure
|
|
Assesment of oxygen saturation after acupressure
Time Frame: after acupressure
|
Vital signs will be monitored immediately after acupressure.
The patient's heart rate will be monitored after acupressure.
The patient's heart rate will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
For most people, a normal pulse oximeter reading for your oxygen saturation level is between 95% and 100%.
|
after acupressure
|
|
Assesment of oxygen saturation after suturing
Time Frame: after suturing
|
vVital signs will be monitored immediately after suturing.
The patient's heart rate will be monitored after suturing.
The patient's heart rate will be monitored on a portable monitor (iMEC 10, Mindray, Chinese).
For most people, a normal pulse oximeter reading for your oxygen saturation level is between 95% and 100%.
|
after suturing
|
|
Assesment of respiratory rate before acupressure
Time Frame: before acupressure
|
Immediately before acupressure, the respiratory rate will be assessed.
The respiratory rate will be counted by observing the chest cage movements for one minute by the researcher (EB).
Vital signs are expected to remain within normal values.
Normal respiration rates for an adult person range from 16 to 20 breaths per minute.
|
before acupressure
|
|
Assesment of respiratory rate after acupressure
Time Frame: after acupressure
|
Immediately after acupressure, After suturing, the respiratory rate will be assessed.
The respiratory rate will be counted by observing the chest cage movements for one minute by the researcher (EB).
Vital signs are expected to remain within normal values.
Normal respiration rates for an adult person range from 16 to 20 breaths per minute.
|
after acupressure
|
|
Assesment of respiratory rate after suturing
Time Frame: after suturing
|
After suturing, the respiratory rate will be assessed.
The respiratory rate will be counted by observing the chest cage movements for one minute by the researcher (EB).
Vital signs are expected to remain within normal values.
Normal respiration rates for an adult person range from 16 to 20 breaths per minute.
|
after suturing
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MU-EBOLAT-804
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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