Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06221436
Other study ID # SBUISTANBUL
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 15, 2024
Est. completion date April 15, 2025

Study information

Verified date April 2024
Source Istanbul Saglik Bilimleri University
Contact Hilal Kartal
Phone 5378870982
Email kartal_hilal@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to examine the effect of olfactory mental imagery on physiological parameters, anxiety and symptoms after cardiovascular surgery. This study was planned to be conducted as a prospective randomized controlled study in the Cardiovascular Surgery service of Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital. The universe of the research; It will consist of patients who are hospitalized in the cardiovascular surgery service and who have undergone cardiovascular surgery. The sample will consist of a total of 90 patients hospitalized in the Cardiovascular Surgery service of the same hospital and meeting the inclusion criteria for the study. Patient Diagnosis Form, Physiological Parameters Monitoring Form, State Anxiety Inventory and Cardiac Surgery Symptom Inventory will be used to collect data. Data will be collected on days 1, 2, 3 and 4 after surgery. In the study, patients will be divided into two groups: intervention (n = 45) and control (n = 45). The intervention group will perform breathing exercises with the olfactory mental imagery technique.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date April 15, 2025
Est. primary completion date January 15, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Elective surgery is planned, - There is no smell problem, - No loss of visual and auditory functions, - No previous hospital history, - No serious head trauma or nasal injury, - No known psychiatric disease or history of anxiolytic drug use, - Olfactory, capable of mental imagery Exclusion Criteria: - Presence of decreased level of consciousness, - Having drainage over 200 ml per hour, - Ejection fraction less than 30 percent, - People with lung disease such as atelectasis and pneumonia, - Systolic blood pressure is below 90 mmHg, - Patients whose pain control cannot be achieved

Study Design


Intervention

Behavioral:
Mental Imagery
Olfactory mental imagery is the ability to detect an odor in the absence of any odor stimulus. Participants will be asked to choose their 4 favorite fragrances from 20 different scents (such as rose, lavender scent) determined by the researcher and proven to have positive effects on mind-body therapy. The determined odors will be visualized by the researcher and picture cards measuring 15X12 cm (for example, a card with a rose picture for the rose smell, etc.) will be created. Participants will visualize the smell by looking at the picture cards, so they will be expected to make their breathing exercises more effective. Vagus breathing technique will be combined with olfactory mental imagery.

Locations

Country Name City State
Turkey Hilal KARTAL Istanbul Beylikdüzü

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Saglik Bilimleri University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vital Signs Observation Form In this form; body temperature value will be evaluated. First 4 days after surgery
Primary Vital Signs Observation Form In this form; respiratory rate will be evaluated. First 4 days after surgery
Primary Vital Signs Observation Form In this form; pulse value will be evaluated First 4 days after surgery
Primary Vital Signs Observation Form In this form; blood pressure value will be evaluated. First 4 days after surgery
Primary Vital Signs Observation Form In this form; oxygen saturation value will be evaluated. First 4 days after surgery
Primary Vital Signs Observation Form In this form; cerebral oxygen saturation value will be evaluated. First 4 days after surgery
Primary State Anxiety Inventory State Anxiety Inventory measures how the individual expresses himself in a momentary situation. The inventory consists of 20 items in total. In this inventory, each item is on a four-point Likert-type scale consisting of '(1) not at all', '(2) a little', '(3) a lot', '(4) completely' and 1. The total score obtained from the inventory varies between 20-80. High scores from the inventory indicate high anxiety. First 4 days after surgery
Secondary Cardiac Surgery Symptom Inventory The inventory consists of 5 subscales: general, cardiac, trunk, lower and upper extremity symptoms. The inventory is in Likert type and is evaluated between 0-4 as "Not at all", "Very little", "Moderate", "A lot", "Quite a lot". The score range to be taken from the inventory varies between 0-140. As scores increase, symptom severity also increases. Seven days after discharge
See also
  Status Clinical Trial Phase
Completed NCT05760482 - Evaluation of the Relationship Between Bruxism and Tryptophan Metabolites N/A
Recruiting NCT04368416 - Anxiety/Depression, Sleep and Alcohol in Elderly Anxiety/Depression, Sleep Disturbances and Alcohol Use Disorder in Elderly With Cognitive Complaints
Completed NCT01190774 - Anxiety Assessment Intervention in Dental Patients Phase 2/Phase 3
Not yet recruiting NCT06418269 - The Effect of Therapeutic Play on Anxiety and Fear Levels in Children With Diabetes N/A
Recruiting NCT06215456 - Virtual Reality to Reduce Periprocedural Anxiety During Invasive Coronary Angiography N/A
Completed NCT06114524 - Effect of Binaural Beats on Level of Anxiety and Toleration in Patients Undergoing Upper Gastrointestinal Endoscopy Without Sedation N/A
Completed NCT05316415 - The Effects of Music on the Anxiety and Sleep Quality of Pregnant Women on Bed Rest for a High-risk Pregnancy N/A
Recruiting NCT05433636 - Mindful Waiting Room N/A
Recruiting NCT06034496 - Cranial Electrotherapy Stimulation and Acute Stress N/A
Recruiting NCT06187090 - The Supplementation Therapy in Autism and Response to Treatment Study N/A
Completed NCT05499767 - HEPPI: Efficacy of a Cognitive-Emotional Intervention for Homebound Older Adults N/A
Not yet recruiting NCT03671317 - Medical Clowns for Pediatric Blood Draw N/A
Terminated NCT03227562 - Is Initial Response to Low Dose Risperidone Predictive for Outcome in Anxiety? Phase 3
Completed NCT04040036 - Effects of Virtual Reality on Pain, Fear and Anxiety During Blood Draw in Children Aged 5-12 Years Old N/A
Completed NCT04568551 - COVID-19-associated Anxiety of Pregnant Women for Anomalies, Stillbirth and Preterm Labor
Recruiting NCT06190184 - Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Conditions N/A
Completed NCT04601545 - The Virtual Reality Therapy as a Pulmonary Rehabilitation Supporting Method N/A
Completed NCT06223412 - Visual Based Program and Climate Change N/A
Recruiting NCT04356638 - a Phase III Trial of Safety and Efficacy of Premedication With Dexmedetomidine and Midazolam in Pediatric Patients Phase 3
Completed NCT03977948 - Qualitative and Systemic Assessment of a Nurse Intervention an Inpatient Child and His or Her Parents