About this trial
This randomized controlled trial aims to evaluate the effect of a mindfulness-based nursing intervention on anxiety levels and vital signs in patients undergoing open-heart surgery during the preoperative and early postoperative periods.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Having a planned elective open heart surgery
Being able to communicate in Turkish and understand the given instructions
Being conscious, cooperative and oriented
Having agreed to participate in the research in the preoperative period
Disqualifiers
Patients with pre-existing serious psychiatric illnesses (e.g., schizophrenia, bipolar disorder)
Patients with cognitive impairment or those unable to complete the STAI-S scale
Patients with neurological or sensory problems that impair hearing, speech, or communication
Patients requiring long-term mechanical ventilation in the postoperative period
Trial design
Parallel
Treatments tested in this trial
Mindfulness-Based Nursing Intervention Group
Other interventionThe mindfulness-based nursing intervention consists of three structured individual sessions delivered by a trained nurse. The first session is conducted one day before surgery, and the second and third sessions are conducted on postoperative day 1 and postoperative day 2, respectively, after extubation when the patient is cooperative and hemodynamically stable. Each session lasts approximately 15-20 minutes and includes guided breathing awareness, relaxation techniques, and brief body awareness exercises adapted to the perioperative cardiac surgery setting. The intervention focuses on present-moment awareness, non-judgmental attention to bodily sensations, and calming of anxiety-related thoughts. All sessions are delivered individually at the patient's bedside in a quiet environment. No prior mindfulness experience is required. The intervention is standardized and applied consistently to all participants in the intervention group.
Standard Care Control Group
Other interventionParticipants in the control group will receive standard perioperative nursing care routinely provided in the cardiovascular surgery clinic. This includes routine preoperative preparation, postoperative monitoring, pain management, and nursing care according to institutional protocols. No additional mindfulness, relaxation, or psycho-educational intervention will be provided.
Treatment groups
Trial outcomes
Primary outcomes
State Anxiety Level (STAI-S)
Anxiety level will be assessed using the State Anxiety subscale of the State-Trait Anxiety Inventory (STAI-S), a validated self-report scale consisting of 20 items. Total scores range from 20 to 80, with higher scores indicating higher levels of anxiety.
Secondary outcomes
Blood Pressure
Systolic and diastolic blood pressure will be measured using standard non-invasive monitoring methods.
Other outcomes
Heart Rate
Heart rate will be recorded as beats per minute using routine clinical monitoring.
Respiratory Rate
Respiratory rate will be measured as breaths per minute through routine clinical observation.
Oxygen Saturation (SpO2)
Peripheral oxygen saturation (SpO2) will be measured as a percentage (%) using pulse oximetry as part of routine monitoring.
Locations
Sponsors and contacts
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