CompletedNot Applicable

Acute Coronary Syndrome and Acupressure

Turkey (Türkiye)68 participantsStarted 2024-05-05

Plain-language summary

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.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Exclusion Criteria: * Those with arrhythmia (AF, VT etc.) * Patients who have previously undergone Coronary Angiography * Diagnosed with myocarditis, pericarditis * Those who do not take any speed-breaking drugs (beloc, arlec, etc.). * Patients who underwent radial intervention for CAG procedure

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

means of blood pressure

Timeframe: up to 30 minutes

means of hear rate

Timeframe: up to 30 minutes

means of respiratory rate

Timeframe: up to 30 minutes

means of cortisol.

Timeframe: up to 60 minutes

Trial details

NCT IDNCT06300294

SponsorAbant Izzet Baysal University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-04-01

View on ClinicalTrials.gov More Acute Coronary Syndrome trials

Plain-language summary

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.