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Clinical Trials in Turkey / NCT07815184
Active, not recruiting Not applicable

Box Breathing and Physiological Feedback Before Endoscopy

NCT07815184 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-15
Last updated
2026-09-11

Condition(s) studied

Breathing ExercisesPhysiological FeedbackStressEndoscopyPatient Comfort

Investigational drug(s) / intervention(s)

Box Breathing Exercise and Real-Time Physiological FeedbackRoutine Maintenance

Box Breathing Exercise and Real-Time Physiological Feedback: A pulse oximeter will be attached to the patient's finger so they can instantly see or sense the relaxing effect. The patient will be asked to monitor changes in their pulse and oxygen levels in relation to their breathing and level of relaxation. The following statement will be made to the patient: "We are now going to do a few minutes of breathing exercises. This exercise will help relax your body, regulate your heart rate, increase your oxygen levels, and help you feel more at ease before the upcoming procedure. All you need to do is follow my breathing instructions and observe your pulse and oxygen levels on the device attached to your finger." Box Breathing Technique (3-4 minutes) Each cycle consists of: inhale for 4 seconds - hold for 4 seconds - exhale for 4 seconds - hold for 4 seconds. Box Breathing Exercise (to be repeated 6-8 times) "Take a deep breath in through your nose 1…2…3…4. Hold your breath 1…2…3…4. Now, exhale slowly 1…2…3…4. Hold your breath out 1…2…3...4

Routine Maintenance: No interventions will be performed on patients in the control group; they will receive routine nursing care before and after the endoscopy.

Study summary

This study aims to evaluate the effects of box breathing exercises and real-time physiological feedback-administered alongside standard nursing care prior to endoscopy-on patients' stress levels, comfort levels, and vital signs. Endoscopy procedures can induce pre-procedural stress and anxiety in patients, potentially affecting their comfort and physiological status. The study will be conducted as a two-group randomized controlled trial. Participants will be randomly assigned to either the study group or the control group. In addition to standard nursing care, the study group will receive guided box breathing exercises and real-time physiological feedback before the endoscopy. The control group will receive only standard nursing care. The study will assess the impact of the intervention on patients' stress levels, comfort levels, and vital signs. It is hypothesized that box breathing exercises and real-time physiological feedback will reduce stress levels, enhance patient comfort, and positively influence vital signs. The findings are expected to contribute to the development of non-pharmacological nursing interventions for managing patient stress and comfort during the pre-endoscopy period.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Individuals who present to the Endoscopy Unit of Mersin City Training and Research Hospital between February 15 and September 15, 2026, * Are aged 18 years or older, * Are literate in Turkish, * Are undergoing a scheduled (non-emergency) endoscopy procedure for the first time, * Do not receive any analgesic or anesthetic medication before or during the procedure, * Have no diagnosis of, nor are receiving medical treatment for, an anxiety disorder, * Have no cognitive, affective, or verbal impairments that would hinder communication, * And agree to participate in the study will be included. Exclusion Criteria: * The following individuals will be excluded, * Those who have previously undergone endoscopy, * Those who have used analgesics within the last 24 hours, * Those scheduled for endoscopy with sedation, * Those using other complementary methods (yoga, reflexology, acupuncture, etc.) during the procedure, * Patients with unstable general condition or vital signs, * Those unable to perform breathing exercises due to severe cognitive impairment or psychiatric illness, * Patients regularly using beta-blockers or antiarrhythmic drugs-making the interpretation of physiological parameters difficult, * Pregnant individuals, * Individuals who do not consent to participate in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Mersin University Institute of Health Sciences Mersin Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07815184 on ClinicalTrials.gov ↗ ← All trials in Turkey