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Search / Trial NCT06636903

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

Launched by EZGI BOLAT · Oct 10, 2024

Trial Information

Current as of July 23, 2025

Not yet recruiting

Keywords

Acupressure, Suturing, Anxiety, Vital Signs, Emergency Department

ClinConnect Summary

This clinical trial is looking at how acupressure, a technique that applies pressure to specific points on the body, can help reduce anxiety in patients who need stitches in the emergency department. Many people feel anxious and scared during this procedure, which can make the experience harder for both them and the healthcare team. The study aims to find out if acupressure can lower anxiety levels and improve vital signs, like blood pressure and heart rate, before getting stitches.

To be part of this study, participants need to be 18 years or older and able to understand and read Turkish. They should not have a diagnosed anxiety condition, be on anxiety medication, or have prior experience with acupressure. Those who agree to join will receive acupressure treatment before their suturing procedure, which could help them feel more relaxed and comfortable. This research could lead to better care for patients in emergency situations by using a safe and simple method to ease their anxiety.

Gender

ALL

Eligibility criteria

  • 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.

About Ezgi Bolat

Ezgi Bolat is a dedicated clinical trial sponsor committed to advancing medical research and innovation through the design and execution of high-quality clinical studies. With a focus on enhancing patient outcomes and ensuring compliance with regulatory standards, Ezgi Bolat collaborates with a network of healthcare professionals and institutions to facilitate the development of effective therapies. Leveraging a rigorous approach to trial management and patient safety, Ezgi Bolat strives to contribute meaningfully to the scientific community and improve healthcare solutions globally.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported