Delirium Clinical Trial
Official title:
The Effect of Psychosocial Nursing Interventions on Sleep, Anxiety and Delirium in Patients Undergoing Open Heart Surgery
The goal of this study is to determine the effects of psychosocial nursing interventions applied to a patient with cardiac surgery on sleep quality, anxiety and delirium. Are psychosocial nursing interventions applied to a patient with cardiac surgery effective in preventing delirium? Are psychosocial nursing interventions applied to a patient with cardiac surgery effective on sleep quality? Are psychosocial nursing interventions applied to a patient with cardiac surgery effective on the level of anxiety?
Status | Recruiting |
Enrollment | 60 |
Est. completion date | November 30, 2023 |
Est. primary completion date | October 30, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: Between 15 April - 31 August 2023, Mersin University Hospital cardiovascular surgery service, cardiovascular surgery intensive care unit was admitted, - over the age of 18, - Patients who will undergo open heart surgery for the first time, - Not diagnosed with any psychiatric disease, - Conscious, cooperative, hemodynamically stable (blood pressure not below 70/50mHg), not on mechanical ventilator - Patients with a state anxiety scale score of 40 and above, - Low and medium risk patients evaluated with the European System for Cardiac Operative Risk Evaluation (EuroSkor), the risk scoring system used to predict mortality in the preoperative period in cardiac surgery, - Literate, with sufficient communication skills and Turkish-speaking - Those who signed the Informed Consent Form to participate in the study will be included. Exclusion Criteria: Between 15 April - 31 August 2023, Mersin University Hospital cardiovascular surgery service, cardiovascular surgery intensive care unit was admitted, - Emergency patients for whom open heart surgery has not been planned before, - Diagnosed with dementia, - Standardized mini mental test (SMMT) below 3 points, - Has a history of previous cerebrovascular accident (CVO), - Severe comorbidity - Patients with a high EuroScore and prolonged mechanical ventilator duration - Those who do not sign the Informed Consent Form to participate in the study will not be included. |
Country | Name | City | State |
---|---|---|---|
Turkey | Firdevs Ebru ÖZDEMIR | Mersin | Yenisehir |
Lead Sponsor | Collaborator |
---|---|
Mersin University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in sleep quality on the Richard Campell Sleep Quality Scale at two days | This scale, developed by Richards, is a 6-item scale that measures the depth of night sleep, the time to fall asleep, the frequency of awakening, the time to stay awake when awakened, the quality of sleep, and the noise level in the environment. Each item is evaluated on a chart with numbers from 0 to 100. According to the scale scoring, "0-25" points indicate very bad sleep, while "76-100" points indicate very good sleep. The 6th item, which evaluates the noise level in the environment, is excluded from the scale total score evaluation, and the total score is evaluated over 5 items. As the score of the scale increases, the sleep quality of the patients also increases. | Baseline and two days | |
Primary | Change from baseline in pain on the Visual Analog Scale at two days | Developed by Price et al. (1983), this scale is one of the commonly used pain measurement tools in health research due to its ease of use and simple structure. The scale consists of a 10 cm ruler on which there is no pain on one end and excruciating pain on the other end, on which the patient marks the pain. The distance between the point where the patient marked the pain and the pain-free interval is measured in cm and recorded. Cline et al., in their study to standardize the VAS, determined that the vertical use of the VAS was better understood by the patients. | Baseline and two days | |
Primary | Change from baseline in anxiety on the State Anxiety Scale at two days | The State-Trait Anxiety Inventory was developed by Spielberger et al. in 1970 to measure state anxiety and trait anxiety. The Turkish validity and reliability study of the scale was performed by Le Compte and Öner in 1983. The "state anxiety" to be used in this study is the subjective fear that the individual feels due to the stressful situation he is in. The state anxiety scale is an easy-to-apply inventory consisting of 20 questions that the individual can answer himself. The individual is asked to mark one of the statements (1) "not at all", (2) "somewhat", (3) "a lot", and (4) "completely", evaluating how he or she feels "at the moment". If the lowest score that can be obtained at the end of the scale is 20, the highest score is 80. In the evaluation, 0-19 points are interpreted as "no anxiety", 20-39 points as "mild anxiety", 40-59 points as "moderate anxiety", 60-79 points as "severe anxiety" and 80 points as "panic value". | Baseline and two days | |
Secondary | Change from baseline in delirium on the Confusion Evaluation in Intensive Care Scale at two days | It is included in the nursing observations, and that delirium could be diagnosed early in the intensive care unit and treated by taking precautions against complications [37]. The scale consists of four items. Sudden change or fluctuation of consciousness in the first item; In the second item, squeezing the hand in less than 12 letters in the attention assessment test tests the two most important signs of delirium, fluctuations in the level of consciousness and deterioration of attention. In the third item, whether the organization of thought is disrupted is evaluated by following four questions and a simple command. The fourth item is about the assessment of the level of consciousness. According to this scale, in order to diagnose delirium, the first two items and one of the third or fourth items must be positive. | Baseline and two days | |
Secondary | Change from baseline in agitation on the Richmand Sedation Agitation Scale at two days | Sessler and others. It was developed by in 2002 to evaluate sedation status in adult ICU patients. In order to be able to evaluate delirium, first of all, the state of consciousness (wakefulness) should be evaluated. It takes ten different values between (+4) and (-5) on the RASS scale. While the ideal level at which the patient is awake and calm is scored with "0" on the scale, scores up to "+4" indicate the increasing agitation of the patient and scores up to "-5" indicate the patient's increasing level of sedation. | Baseline and two days |
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