Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06572670

The Effect of Progressive Relaxation Exercise Performed Before Coronary Angiography

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.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Progressive relaxation exercise before coronary angiography

Other

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

Primary outcomes

  1. Anxiety level

    Time frame: 30 minutes after angiography

    This 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.

  2. Comfort level

    Time frame: 30 minutes after angiography

    The 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.

  3. Pain level

    Time frame: 30 minutes after angiography

    Pain 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 outcomes

  1. Blood pressure to be assessed with monitor

    Time frame: 30 minutes after angiography

    The patient's blood pressure will be measured from the brachial artery with a bedside monitor and the result will be recorded in mmHg.

  2. Pulse to be assessed with monitor

    Time frame: 30 minutes after angiography

    Heart rate will be measured with a bedside monitor that can be measured from a finger and recorded as beats/min.

  3. Respiratory rate

    Time frame: 30 minutes after angiography

    Respiratory rate will be measured by counting the number of inspirations and expiration from the patient's chest movements.

Sponsors and collaborators

Lead sponsor

TC Erciyes University

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Aug 27, 2024
Registry last updated
Aug 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.