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NCT06300294Completed

Acute Coronary Syndrome and Acupressure

The Effect of Acupressure on Anxiety And Physiological Parameters in Individuals Diagnosed With Acute Coronary Syndrome: A Randomized Controlled Study

Source: ClinicalTrials.gov · Last updated 26 May 2026

Brief summary (registry, in English)

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 with ACS has an effect on blood pressure. H1-2: Acupressure applied to individuals with ACS has an effect on heart rate. H1-3: Acupressure applied to individuals with ACS has an effect on respiratory rate. H1-4: Acupressure applied to individuals with ACS has an effect on pain levels. H1-5: Acupressure applied to individuals with ACS has an effect on anxiety levels. H1-6: Acupressure applied to individuals with ACS has an effect on cortisol levels. H1-7: Acupressure applied to individuals with ACS has an effect on ECG changes.

Status (registry)
Completed
Study type
Interventional
Enrollment
68 (actual)
First submitted
14 Feb 2024
Start date
May 2024
Primary completion date
Apr 2025
Lead sponsor
Abant Izzet Baysal University
NCT number
NCT06300294

What you commit to

  • Study type: Interventional
  • Participants enrolled: 68
  • From May 2024 to the primary completion date, Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have previously undergone Coronary Angiography
  • Those who do not take any speed-breaking drugs (beloc, arlec, etc.).

Other illness

  • Those with arrhythmia (AF, VT etc.)

Other

  • Diagnosed with myocarditis, pericarditis
  • Patients who underwent radial intervention for CAG procedure

Who the study is looking for

  • Volunteer to participate in the study,
    • Those aged 18 and over
    • Able to speak Turkish
    • Diagnosed with ACS for the first time
    • Cardiopulmonary resuscitation not applied
    • No orientation problems (those who score 15 on the Glasgow Coma Scale)
    • Not diagnosed with psychiatric disease
    • No amputation, fistula, lymphedema, neuropathy or hemiplegia in any of the Upper Extremities
    • Those who underwent femoral intervention for CAG procedure
    • Those who have not used any integrative practices based on pressure and stimulation such as acupressure, acupuncture and reflexology in the last month.
    • Vital signs (28) are within normal range:
    • Blood pressure: 90/60-120/80 mmHg Heart rate: 60-100 min Respiratory rate: 12-18 min

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Manisa City Hospital
Coordinator of this site? Confirm its status
ManisaTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.