Effect of Virtual Reality Glasses on Stress, Muscle Tension, and Physiological Parameters Before Angiography

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorYuksek Ihtisas University

About this trial

Today, cardiovascular diseases are the leading cause of morbidity and mortality worldwide. Coronary angiography (CAG), a commonly used invasive procedure for diagnosing coronary artery disease, may trigger fear, stress, and anxiety in patients due to its invasive nature, lack of information, uncertainty, and the possibility of receiving a life-threatening diagnosis.These emotional responses activate stress mechanisms, leading to catecholamine release, increased heart rate, blood pressure, respiration, sweating, and muscle tension. Elevated stress can also cause lactic acid accumulation, increased oxygen demand, and muscular contraction, potentially resulting in coronary artery spasms or arrhythmias, and increasing procedural risks. Therefore, reducing stress before CAG is crucial to improving procedural outcomes and patient recovery.

To address preoperative anxiety and stress, both pharmacologic and non-pharmacologic interventions are used. Among the non-pharmacologic options, virtual reality (VR) has emerged as an effective method to distract and calm patients, reducing anxiety, stress, and pain. Studies in various patient populations suggest VR glasses can be beneficial in managing psychological distress. However, no study has been found in the literature evaluating the effect of VR on stress-induced muscle tension in patients undergoing CAG. This gap highlights the potential contribution of this study to current knowledge.

This study aims to investigate the effect of using VR glasses before coronary angiography on patients' stress levels, muscle tension, and selected physiological parameters.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

18-65 years of age,

Scheduled to undergo CAG,

American Society of Anesthesiologists (ASA) score I or II,

Turkish-speaking patients will be included.

Disqualifiers

with dizziness,

with headache,

with any known psychiatric disease and mental perception problem,

pregnant,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Intervention application with virtual reality glasses

    Behavioral

    In the preoperative period, approximately 1 hour before the procedure, a video will be watched for 15 minutes with virtual reality glasses. Approximately 10 minutes before the procedure, the patients will be administered the Physiological Parameters Monitoring Form, Distress Thermometer and VAS, and the data collection process will be completed.

  • Standard application

    Behavioral

    No intervention will be made to the patients outside of the hospital routine, and approximately 10 minutes before the procedure, the Physiological Parameters Monitoring Form, Distress Thermometer and VAS will be applied again and the data collection process will be completed.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Control GroupOther 1 intervention
Group B: Experimental GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Distress Thermometer

It is a Likert-type scale with scores from 0 (no stress) to 10 (extreme stress) developed by Roth et al. (1998) to determine psychological distress in cancer patients. In the short and easy-to-understand scale, patients can easily mark their own stress levels within the specified ranges on the thermometer. The Turkish validity-reliability study of the Distress Thermometer was conducted by Özalp et al. (2007) . In their study, Özmen and Gürsoy (2021) concluded that the distress thermometer can be used as a valid and reliable measurement tool to measure the stress experienced by patients who will undergo surgery. With this scale, the stress levels of the patients in the last week and at the time of evaluation will be evaluated.

Time frame
Preoperative period
2

Assessment of Muscle Tension

Measuring patients' symptomatic experiences through questionnaires or self-reports is the gold standard method for assessing the presence and severity of a mental disorder. In a study conducted by Sainsbury and Gibson (1954) on symptoms reported by anxious, stressed patients, "feeling of tension" was mostly defined as "feeling of tension in the muscles," "muscle stiffness," "cramping," and "body discomfort" line with this information, the 10-point Visual Analogy Scale (VAS) will be used to assess muscle tension resulting from stress in patients before the CAG procedure, and patients will be asked to rate their feelings of tension in the muscles, stiffness in the muscles, cramping in any muscle, and inability to relax their body using this scale. This scale is 10 centimeters (cm) long and includes numbers from 0 to 10. The values marked by the patient between 0-10 cm on the scale will be ta

Time frame
Preoperative period
3

Physiological Parameters Monitoring Form

This form includes questions about patients' systolic and diastolic blood pressure

Time frame
Preoperative period
4

Physiological Parameters Monitoring Form

This form includes question about patients' pulse

Time frame
Preoperative period

Secondary outcomes

1

Distress Thermometer

The patients were reapplied approximately 10 minutes before the procedure to measure their stress levels.

Time frame
Approximately 10 minutes before the procedure, patients
2

Assessment of Muscle Tension

Patients will be asked to rate whether they feel tension in their muscles, a feeling of stiffness in their muscles, a feeling of cramping in any muscle, or an inability to relax their body.

Time frame
About 10 minutes before entering the process
3

Physiological Parameters Monitoring Form

Approximately 10 minutes before the procedure, patients are asked questions about their systolic and diastolic blood pressure

Time frame
About 10 minutes before entering the process
4

Physiological Parameters Monitoring Form

Approximately 10 minutes before the procedure, patients are asked question about pulse

Time frame
About 10 minutes before entering the process

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: