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NCT ID: NCT05358223 Recruiting - Prostate Biopsy Clinical Trials

Pain and Anxiety During Transrectal Prostate Biopsy

Start date: March 14, 2022
Phase: N/A
Study type: Interventional

Many studies have been conducted in the literature to manage pain and anxiety levels for patients undergoing transrectal prostate biopsy. In addition to the periprostatic block application recommended in the guidelines of the European Association of Urology, there are studies showing that TENS application or music applications will make an additional contribution.However, there is no study comparing the effect of TENS and music.

NCT ID: NCT05358197 Not yet recruiting - Sleep Quality Clinical Trials

Effect of Laughter Yoga on Sleep Quality and Happiness

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

In this study, the effect of laughter yoga on sleep quality and happiness level in individuals with sleep problems will be investigated. Yoga exercises will be done for about 30 minutes with a laughter yoga instructor 3 days a week for a month.

NCT ID: NCT05357976 Completed - Pain, Postoperative Clinical Trials

The Effects of Body Mass Index on Thoracic Paravertebral Block Analgesia

Start date: April 25, 2022
Phase: N/A
Study type: Interventional

Obesity has become one of the world's leading health problems. It is known that obesity causes many diseases and negatively affects the quality of life. For this reason, many conditions that are thought to be effective in obesity and concern the quality of life of patients have been scientifically researched and continue to be investigated. One of them is postoperative pain. Although there are studies stating that there is no relationship between body mass index (BMI) and postoperative pain, when the literature data is examined, it is thought that obesity is a risk factor for postoperative pain and changes pain sensitivity and analgesic needs of patients. There are also studies in the literature stating that the level of postoperative pain increases in parallel with each unit increase in BMI. After thoracic surgery, many analgesic methods have been suggested, including thoracic epidural analgesia (TEA), thoracic paravertebral block (TPVB), intercostal nerve blocks (ICSB), erector spina plane block (ESPB), serratus anterior plane block (SAPB). This study will compare the effects of BMI on postoperative pain in patients undergoing TPVB for postoperative analgesia and thoracoscopic surgery.

NCT ID: NCT05357963 Recruiting - Postoperative Pain Clinical Trials

Incidence of Chronic Pain After Sternotomy

Start date: April 20, 2022
Phase:
Study type: Observational

Chronic postoperative pain is a well-known problem. Chronic postoperative pain is defined as pain that begins following a surgical procedure and persists for more than 2 months without other obvious causes such as infection or underlying disease. Sternotomy causes significant postoperative pain, and patients with chronic pain after sternotomy are often referred to pain clinics. The incidence of chronic pain after sternotomy ranges from 17% to 56%; In approximately one-third of these patients, chronic pain after sternotomy can compromise their quality of life by affecting their sleep patterns and impairing their ability to work. However, epidemiological studies on chronic pain after sternotomy are scarce. The aim of this study is to examine the incidence and possible risk factors of chronic pain following sternotomy operations. In this study, it was aimed to analyze the chronic pain findings of the patients who underwent sternotomy in the postoperative 3rd month.

NCT ID: NCT05356832 Recruiting - Clinical trials for Urinary Incontinence

Investigation of the Relationship Between Pelvic Floor Awareness and Urinary Incontinence

Start date: January 1, 2022
Phase:
Study type: Observational

There is no study in the literature examining the knowledge level and urinary symptoms of active athletes about the pelvic floor. The aim of this study is to determine the relationship between PTC awareness and incontinence in young athletes who engage in long-term and high-intensity activities that increase the risk of SUI.

NCT ID: NCT05356819 Completed - Clinical trials for Monitored Anesthesia Care

The Value of Integrated Pulmonary Index Monitoring in Detecting Respiratory Events

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Integrated Pulmonary Index (IPI) is a tool that provides numerical values on a scale of 1-10 based on physiological parameters such as peripheral oxygen saturation (SpO2), pulse rate, respiratory rate, end-tidal carbon dioxide (ETCO2). It is a valuable monitor for sedation procedures and can provide early warning during cardiorespiratory derangements.The aim of the study is to determine whether the Integrated Pulmonary Index (IPI) detects changes in ventilation status early in patients undergoing gastrointestinal endoscopy under sedation, and to determine the risk factors affecting hypoxia and severe hypoxia.

NCT ID: NCT05356455 Completed - Loneliness Clinical Trials

Motivational Interviewing Technique on Loneliness Levels in University Students Aged 18-25 Living Far From Home

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

Purpose of the research This research was planned to evaluate the effect of motivational interview technique on loneliness in university students aged 18-25 living far from home.

NCT ID: NCT05356273 Completed - Clinical trials for Hyperbilirubinemia, Neonatal

The Effect of Massage on the Bilirubin Level in Term Infants Receiving Phototherapy

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

Background: It has been reported in the current literature that massage has various positive physiological effects on the newborn. Also baby massage; It increases the collection and excretion of waste products such as bilirubin by accelerating the flow of blood, lymph and tissue fluids. Our aim is to investigate the effect of infant massage on hyperbilirubinemia in newborns receiving phototherapy. Method: The population of the study consisted of babies who were hospitalized in Istanbul Haseki Training and Research Hospital Neonatal Intensive Care Unit between October 2021 and January 2022 and needed phototherapy. Transcutaneous bilirubin device and data collection form were used to obtain the data. 61 newborns who met the study criteria were randomly divided into experimental (n=30) and control (n=31) groups. Phototherapy was applied to all babies twice a day. In addition to phototherapy, infant massage was applied to the experimental group for 10 minutes just before the phototherapy. Bilirubin level measurements were made 2 hours after the end of phototherapy for both groups. Diaper changes for both groups were carried out 8 times a day, every 3 hours.

NCT ID: NCT05356065 Completed - Sports Injury Clinical Trials

The Turkish Version of the OSTRC Questionnaires

Start date: January 26, 2021
Phase:
Study type: Observational [Patient Registry]

Exposure to repetitive activities and heavy workloads makes athletes vulnerable to overuse injuries over time. Well-timed detection of these injuries is crucial to maintaining their sports career healthily. The Oslo Sports Trauma Research Centre questionnaires for Overuse Injury (OSTRC-O) and Health Problems (OSTRC-H) are universally used as valid and reliable tools in athlete health screening. This study aims to make them available for Turkish athletes. The internal consistency, reproducibility, and validity of the questionnaires were analyzed. Data were obtained from 72 athletes from different sports types. 33 participants were screened weekly for six weeks to detect score changes and calculate effect sizes. Participants filled out the OSTRC-O, the OSTRC-H, the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ), and the Nottingham Health Profile (NHP) for validity analyses. The internal consistency and test-retest reliability values were very high for both questionnaires. There was a moderate correlation between OSTRC-O and OSTRC-H scores with CMDQ and NHP. The area under the curve (AUC) values were adequate for all scales. The effect size values were moderate for all scales. Turkish versions of the OSTRC-O and OSTRC-H questionnaires are valid and reliable tools for Turkish-speaking athletes in different sports branches.

NCT ID: NCT05356026 Completed - Clinical trials for Postpartum Depression

Online Postpartum Follow-up on Depression and Postpartum Adaptation

Start date: March 10, 2021
Phase: N/A
Study type: Interventional

Objective: To determine the effect of online postpartum follow-up on depression and postpartum adaptation. Design: A parallel-randomized-controlled study Setting: During 2021 in Turkey Participants: 52 women in the postpartum period Measurements: Data were collected through the Personal Information Form, the Follow-up Form, the Edinburgh Postpartum Depression Scale (EPDS), and the Postpartum Self-Assessment Scale (PSAS). The women in the experimental group were administered three follow-ups (education/consultancy) in line with the timing and content in the T.R. Ministry of Health Postpartum Care Management Guide (2014). The follow-ups were performed using the Zoom® program, which enabled video talk. The women in the control group received the routine follow-up and care provided by the hospital.