Not yet recruiting NCT06572670

The Effect of Progressive Relaxation Exercise Performed Before Coronary Angiography

No phase Interventional Coronary Angiography Progressive Relaxation Exercise Nursing

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Progressive relaxation exercise before coronary angiography.
Who it may be relevant to: Registry conditions: Coronary Angiography, Progressive Relaxation Exercise, Nursing. Basic parameters: 18 years — 75 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Center list to be confirmed — check the primary protocol.
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

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

Overview

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

Interventions

Other Progressive relaxation exercise before coronary angiography
Patients in the intervention group will undergo progressive relaxation before undergoing angiography.

Primary outcome measures

Anxiety level [Time frame: 30 minutes after angiography]
Comfort level [Time frame: 30 minutes after angiography]
Pain level [Time frame: 30 minutes after angiography]

Secondary outcome measures (3)

Blood pressure to be assessed with monitor [Time frame: 30 minutes after angiography]
Pulse to be assessed with monitor [Time frame: 30 minutes after angiography]
Respiratory rate [Time frame: 30 minutes after angiography]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation: Randomized
Model: Parallel assignment
Masking: Open label
Primary purpose: Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06572670 · 2024/30

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗