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The effect of acupressure on acute coronary syndrome

The effect of acupressure on chest pain, anxiety and vital signs in the elderly with acute coronary syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240723062519N2
Enrollment
110
Registered
2024-11-12
Start date
2024-10-22
Completion date
Unknown
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute coronary syndrome.

Interventions

Intervention 1: Intervention group: Gentle pressure for 5 minutes will be applied to the three pressure points of Shen Men, Yin Tong, and HT7 point for the patients. Intervention 2: Control group: In

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Age 60 years and older Willingness to participate in the study Both genders Definitive diagnosis of heart pain by an emergency physician Patient alertness Pain score of 3 and above and 8 and below 8 Patients with unstable angina and without ascending St Not having any wounds on the body Not having a history of heart attack No having a history of diabete Failure of the patient to go to the emergency room by the 115 medical emergency team

Exclusion criteria

Exclusion criteria: Acute heart attack The patient's loss of consciousness upon entering the emergency room or during the implementation of the intervention Death or unwillingness to continue cooperation for any reason Having a known mental illness such as anxiety Addiction to smoking, alcohol and drugs Having an anatomical problem at the location of acupressure points Having a history of previous heart attack

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before the intervention, immediately after the intervention, 10 minutes after the intervention, 20 minutes after the intervention, 30 minutes after the intervention. Method of measurement: Numerical pain intensity measurement scale.;Anxiety. Timepoint: Before the intervention, immediately after the intervention, 10 minutes after the intervention, 20 minutes after the intervention, 30 minutes after the intervention. Method of measurement: DASS-21 stress, anxiety and depression questionnaire, anxiety subscale.;Vital signs. Timepoint: Before the intervention, immediately after the intervention, 10 minutes after the intervention, 20 minutes after the intervention, 30 minutes after the intervention. Method of measurement: Vital signs chart sheet using bedside monitoring in the emergency department.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Hossein Abadi

Khoram-Abad University of Medical Sciences

Reza_hosseinabadi@yahoo.com+98 66 3312 0174

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026