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The Effect of Progressive Relaxation Exercise Performed Before Coronary Angiography

The Effect of Progressive Relaxation Exercise Performed Before Coronary Angiography on Anxiety, Comfort, Pain and Physiological Parameters

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06572670
Enrollment
70
Registered
2024-08-27
Start date
2024-09-15
Completion date
2025-02-15
Last updated
2024-08-27

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

Conditions

Coronary Angiography, Nursing, Progressive Relaxation Exercise

Brief summary

This study was planned to examine the effects of progressive relaxation exercise on anxiety, comfort, pain and physiological parameters in patients undergoing coronary angiography. The data of the study will be collected using the Descriptive Characteristics Questionnaire Form, State and Trait Anxiety Inventory, Perianesthesia Comfort Questionnaire, Visual Analog Scale (VAS), Vital Signs Follow-up Form, Complication Follow-up Form and Progressive Relaxation Exercise Application Guidelines.

Detailed description

This study was planned to examine the effects of progressive relaxation exercise on anxiety, comfort, pain and physiological parameters in patients undergoing coronary angiography. The data of the study will be collected using the Descriptive Characteristics Questionnaire Form, State and Trait Anxiety Inventory, Perianesthesia Comfort Questionnaire, Visual Analog Scale (VAS), Vital Signs Follow-up Form, Complication Follow-up Form and Progressive Relaxation Exercise Application Guidelines. Patients in the intervention group will undergo progressive relaxation before undergoing angiography. Standard practices of the clinic will be applied to the control group.

Interventions

OTHERProgressive relaxation exercise before coronary angiography

Patients in the intervention group will undergo progressive relaxation before undergoing angiography.

Sponsors

TC Erciyes University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients who can speak and understand Turkish, * Are over 18 years old, * Have space and time orientation, * Will undergo coronary angiography for the first time, * Do not have any psychiatric illness, * Do not have vision or hearing problems, * Volunteer to participate in the study will be included.

Exclusion criteria

* Patients who experience any pain or have chronic pain before coronary angiography, * Patients who use antihistamines and psychiatric medications, * Patients who do not volunteer to participate in the study, * Patients who have undergone orthopedic surgery or have any medically diagnosed health problems (orthopedic, neurological, psychological) that prevent relaxation exercises, * Patients who have taken sedatives or painkillers up to 5 hours before coronary angiography will not be included in the study.

Design outcomes

Primary

MeasureTime frameDescription
Anxiety level30 minutes after angiographyThis inventory, which consists of a total of 40 items, is analyzed in two separate sections: The first part is the State Anxiety Inventory, which consists of 20 items, and the individual answers this section with his/her current feelings. The second part is the Trait Anxiety Inventory, which also consists of 20 items, and the individual answers this section with the feelings they have felt in the last 7 days.
Comfort level30 minutes after angiographyThe scale, which is based on the concept of comfort, consists of a total of 24 items, 12 of which question the comfort status of the individual before and after the surgical intervention, 12 of which question positive and 12 of which question negative experiences.
Pain level30 minutes after angiographyPain will be assessed with the Visual Analog Scale. This scale consists of a 10 cm line with values between 0 and 10. The beginning of the line (number 0) indicates no pain, while the end of the line (number 10) indicates the most severe pain.

Secondary

MeasureTime frameDescription
Blood pressure to be assessed with monitor30 minutes after angiographyThe patient's blood pressure will be measured from the brachial artery with a bedside monitor and the result will be recorded in mmHg.
Pulse to be assessed with monitor30 minutes after angiographyHeart rate will be measured with a bedside monitor that can be measured from a finger and recorded as beats/min.
Respiratory rate30 minutes after angiographyRespiratory rate will be measured by counting the number of inspirations and expiration from the patient's chest movements.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026