Effect of Acupressure Applied Before CAG on Pain, Anxiety and Vital Signs

NCT ID: NCT06916351

Last Updated: 2025-04-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

93 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-01

Study Completion Date

2024-12-31

Brief Summary

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This randomized controlled experimental study aimed to determine the effects of acupressure applied before the procedure on pain, anxiety and vital signs in patients who applied to Kocaeli City Hospital Angiography Unit and were to undergo planned radial artery coronary angiography.

Detailed Description

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This randomized controlled experimental study was conducted at the Kocaeli City Hospital Angiography Unit to determine the effects of acupressure applied before coronary angiography on pain, anxiety and vital signs of the patients scheduled to undergo coronary angiography. It was conducted at the Kocaeli City Hospital Angiography Unit. The study used a stratified block randomization method and 93 patients who met the inclusion criteria were assigned to two different intervention groups, one of which received acupressure and the other a sham intervention before coronary angiography, and a control group receiving standard care. Data were collected using the 'Personal Information Form', 'State Anxiety Inventory (STAI)', 'Visual Analog Scale (VAS)' and 'Patient Follow-up Form'.

Conditions

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Acupressure Coronary Angiography and Intervention

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

It is a single-blind, parallel group, pre-test-post-follow-up randomized controlled experimental study.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants
The participant does not know which group he/she is in.

Study Groups

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Sham acupressure

Sham acupressure will be applied to three points parallel to HT7, LI4 and PC6, approximately 1-1.5 cm away from the meridians. To prepare the points for acupressure, these points will be rubbed for approximately 20-30 seconds without applying direct pressure, reducing tissue sensitivity. The researcher will then apply acupressure to these points and symmetrical points using the thumb for three minutes, but will apply less pressure than required levels. Similar to the acupressure group, preparations and acupressure application will take approximately 20 minutes in total for each patient.

Group Type PLACEBO_COMPARATOR

Sham acupressure

Intervention Type OTHER

Sham acupressure will be applied to three points parallel to HT7, LI4 and PC6, approximately 1-1.5 cm away from the meridians.

Control

Patients in the control group will not receive any intervention and will receive routine treatment and care.

Group Type NO_INTERVENTION

No interventions assigned to this group

Acupressure

Acupressure will be applied to a total of three points, namely HT7, LI4, and PC6, determined by the researcher with a certificate according to literature and expert opinion before the CAG procedure for the acupressure group. The "cun" measurement unit will be used to determine the points where the application will be made. Before the application, after approximately 20-30 seconds of heating and rubbing without direct pressure on the acupressure points, the researcher will manually press the determined acupressure points with the thumb for 10 seconds to create a depth of 1-1.5 cm. Pressure will be applied to each acupressure point for three consecutive minutes (in the breathing rhythm) without lifting the finger, allowing for two seconds of relaxation. Since the symmetry of the three different points selected on the other extremity will also be applied, a total of 18 minutes of pressure will be applied to each point, with the condition of three minutes.

Group Type EXPERIMENTAL

Acupressure

Intervention Type OTHER

Acupressure will be applied to a total of three points: the 4th point of the Large Intestine Meridian (LI4-Hegu point) and the 6th point of the pericardial meridian (PC6- Nei Guan point), located three fingers above the wrist.

Interventions

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Acupressure

Acupressure will be applied to a total of three points: the 4th point of the Large Intestine Meridian (LI4-Hegu point) and the 6th point of the pericardial meridian (PC6- Nei Guan point), located three fingers above the wrist.

Intervention Type OTHER

Sham acupressure

Sham acupressure will be applied to three points parallel to HT7, LI4 and PC6, approximately 1-1.5 cm away from the meridians.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Over 18 years of age,
* Able to understand and speak Turkish,
* Open to communication,
* First time undergoing radial artery coronary angiography,
* Elective patients undergoing planned (non-urgent) coronary angiography,
* Patients who did not undergo stent/balloon intervention during angiography,
* Awake and conscious during coronary intervention (not having taken sedatives (dormicum/fentanyl))
* No deformities or lesions in the areas where acupressure will be applied (hematoma, ecchymosis, etc.)
* Having not taken sedatives or painkillers 5 hours before the angiography,
* No experience with acupressure,
* No history of attending training courses and yoga classes to control stress and anxiety in the last six months
* No diagnosis of anxiety disorder and not receiving medical treatment
* No diagnosis of depression and not receiving medical treatment
* Flat on the back (patients without respiratory distress, etc.),
* Hemodynamically stable (no chest pain or arrhythmia),
* Patients who volunteer to participate in the study,

Exclusion Criteria

* Diagnosed with any psychiatric disease
* Previously undergone coronary angiography from the radial or femoral artery
* Chronic pain
* Used opioid medication
* CAG procedure to be performed from the femoral artery
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bandırma Onyedi Eylül University

OTHER

Sponsor Role lead

Responsible Party

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Sarenur Ozen

Nurse, graduate student

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kocaeli City Hospital

Kocaeli, İzmit, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Ethics Committee

Identifier Type: OTHER

Identifier Source: secondary_id

BandirmaOnyediEylul University

Identifier Type: -

Identifier Source: org_study_id

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