Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06300294

Acute Coronary Syndrome and Acupressure

Led by Abant Izzet Baysal University · Updated on 2024-10-10

38

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to examine the effect of acupressure on physiological parameters and anxiety levels in individuals diagnosed with Acute Coronary Syndrome (ACS). H1-1: Acupressure applied to individuals diagnosed with ACS has an effect on the level of anxiety. H1-2: Acupressure applied to individuals diagnosed with ACS has an effect on blood pressure. H1-3: Acupressure applied to individuals diagnosed with ACS has an effect on heart rate. H1-4: Acupressure applied to individuals diagnosed with ACS has an effect on respiratory rate. H1-5: Acupressure applied to individuals diagnosed with ACS has an effect on the pain level. H1-6: Acupressure applied to individuals diagnosed with ACS has an effect on cortisol levels.

CONDITIONS

Official Title

Acute Coronary Syndrome and Acupressure

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Volunteer to participate in the study
  • Aged 18 years or older
  • Able to speak Turkish
  • Diagnosed with Acute Coronary Syndrome for the first time
  • Has not had cardiopulmonary resuscitation
  • No orientation problems (Glasgow Coma Scale score of 15)
  • Not diagnosed with psychiatric disease
  • No amputation, fistula, lymphedema, neuropathy, or hemiplegia in any upper extremities
  • Underwent femoral intervention for coronary angiography procedure
  • Has not used any integrative pressure-based practices such as acupressure, acupuncture, or reflexology in the last month
  • Vital signs within normal range: Blood pressure 90/60-120/80 mmHg, Heart rate 60-100 beats per minute, Respiratory rate 12-18 breaths per minute
Not Eligible

You will not qualify if you...

  • Diagnosed with arrhythmia (e.g., atrial fibrillation, ventricular tachycardia)
  • Previously undergone coronary angiography
  • Diagnosed with myocarditis or pericarditis
  • Not taking any speed-lowering drugs (e.g., Beloc, Arlec)
  • Underwent radial intervention for coronary angiography procedure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Manisa City Hospital

Manisa, Turkey (Türkiye), 45000

Actively Recruiting

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Research Team

H

hospital Chief physician, Dr

CONTACT

S

saadet can çiçek, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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