[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"KTO Karatay University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":433},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,16,0,[8,41,63,87,122,149,169,198,223,250,271,300,332,357,385,410],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100630462","acute-effects-of-motor-imagery-and-motor-control-exercises-in-individuals-with-chronic-neck-pain-100630462",false,"NCT07487987","Acute Effects of Motor Imagery and Motor Control Exercises in Individuals With Chronic Neck Pain","Comparison of the Acute Effects of Motor Imagery and Motor Control Exercises in Individuals With Chronic Neck Pain","Inclusion Criteria:\n\n* Neck pain lasting at least 12 weeks,\n* VAS score of at least 3 cm,\n* Standardized Mini Mental Test score of at least 24.\n\nExclusion Criteria:\n\n* History of cervical surgery,\n* neurological deficit,\n* malignancy,\n* rheumatic diseases,\n* having received physical therapy for the neck region within the last 3 months","ALL","18 Years","65 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of this study is to compare the effects of single-session motor imagery and motor control exercises on pain, pressure pain threshold, cervical proprioception, and motor imagery in individuals with chronic neck pain.",[27],"Chronic Neck Pain","RECRUITING","2026-07-01",{"date":31,"type":32},"2026-07-02","ACTUAL",{"date":34,"type":32},"2026-03-10",{"date":36,"type":21},"2026-09-14",{"name":38,"class":39},"KTO Karatay University","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":48,"sex":16,"minAge":18,"maxAge":49,"enrollmentInfo":50,"targetDuration":52,"studyType":53,"phases":4,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":57,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":40},"100624880","frailty-dual-task-performance-and-activities-of-daily-living-in-older-adults-100624880","NCT07415382","Frailty, Dual-Task Performance, and Activities of Daily Living in Older Adults","The Relationship Between Frailty, Dual-Task Performance, and Activities of Daily Living in Older Adults","Inclusion Criteria:\n\n* Be 65 years of age or older,\n* Be literate\n* Have a Mini Mental State Examination (MMSE) score of 24 or higher (cognitively sound)\n* Be able to walk at least 10 meters without the use of assistive devices,\n* Not have advanced sensory loss that impairs vision or hearing.\n\nExclusion Criteria:\n\n* Having a severe neurological (Parkinson's, stroke, etc.) or orthopedic disorder,\n* Having a psychiatric diagnosis that prevents communication.",true,"85 Years",{"count":51,"type":21},200,"1 Day","OBSERVATIONAL","This study aims to examine the relationship between dual task performance, frailty level, and activities of daily living in older adults.",[56],"Older Adults (60 - 85 Years Old)",{"date":31,"type":32},{"date":59,"type":32},"2026-02-07",{"date":61,"type":21},"2026-08-30",{"name":38,"class":39},{"id":64,"slug":65,"hasResults":11,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":4,"eligibilityCriteria":69,"healthyVolunteers":11,"sex":70,"minAge":71,"maxAge":72,"enrollmentInfo":73,"targetDuration":4,"studyType":22,"phases":75,"briefSummary":76,"conditions":77,"keywords":4,"overallStatus":80,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":85,"leadSponsor":86,"locationsCount":40},"100596435","the-effect-of-pelvic-floor-muscle-exercises-after-radical-prostatectomy-100596435","NCT07045415","The Effect of Pelvic Floor Muscle Exercises After Radical Prostatectomy","The Effect of Pelvic Floor Muscle Exercises on Urinary Incontinence Management and Quality of Life in Patients Undergoing Radical Prostatectomy","Inclusion Criteria:\n\n* Being 40 years of age or older Not having urinary incontinence before surgery Having undergone Radical Prostatectomy surgery due to prostate cancer Patients who did not have urinary incontinence before surgery\n\nExclusion Criteria:\n\n* Patients with congenital anomalies of the urinary system, serious organ dysfunctions (liver or kidney failure, advanced heart failure, coagulopathy), neuropsychiatric disorders, presence of active infection, and history of major abdominal or pelvic surgery will not be included in the study.","MALE","40 Years","90 Years",{"count":74,"type":21},10,[24],"Cancer, a major public health problem worldwide, was one of the leading causes of mortality in 2020, accounting for approximately 10 million deaths. With 1.41 million new cases reported in the same year, prostate cancer is the fourth most common cancer type globally (Ferlay et al., 2021). Prostate cancer is not only one of the most common types of cancer in men, but it also ranks second among cancer-related deaths in men worldwide (Rahnama'i et al., 2021). Radical prostatectomy (RP) is a treatment method that involves the surgical removal of the prostate gland and surrounding tissues, to stop the progression of the disease and improve the patient's quality of life (Göktas et al., 2015; Litwin and Tan, 2017). Following radical prostatectomy, a curative treatment method commonly used to prevent metastasis, mortality rates remain low; however, the procedure carries a relatively high risk of morbidity (Akarken et al., 2020; Evren and Taşcı, 2021).\n\nThe most common complication encountered by patients after RP is urinary incontinence (Choiniere et al., 2022; Rahnama'i et al., 2021). Urinary incontinence (UI) arises due to factors such as damage to the internal sphincter, external rhabdosphincter, and supportive structures of the urethra during surgery, as well as the involvement of the neurovascular bundle and the development of postoperative fibrosis (Castellan et al., 2023). UI developing after radical prostatectomy significantly reduces patients' quality of life and negatively affects their social adaptation. Therefore, understanding the factors influencing the development of UI after radical prostatectomy is of great importance in determining appropriate treatment approaches and optimizing management (Bernardes et al., 2019; Storås et al., 2020). In the literature, the incidence rates of incontinence after radical prostatectomy range from 0.8% to 87%, and these differences are attributed to various factors such as surgical technique, patient characteristics, and evaluation methods (Boorjian et al., 2012; Hodges et al., 2019; Grise et al., 2017; Pastero et al., 2017).\n\nIn the majority of patients, moderate to severe urinary incontinence is observed in the first few weeks after surgery. In some patients, this condition may persist for months or even years. Urinary incontinence can lead to various psychosocial effects such as shame, loss of self-esteem, impaired mental well-being, anxiety, relationship and sexual dysfunction, and social isolation (Kadono et al., 2016; Zachovajeviene et al., 2017). This condition has a significant impact on patients' physical, social, and emotional well-being, as well as their daily activities, and can contribute to social isolation by causing feelings of embarrassment (Castellan et al., 2023; Ouanes et al., 2022).\n\nNurses play an important role in the management of urinary incontinence that develops after RP. Nurses can educate patients about urinary incontinence, teach conservative treatment methods such as pelvic floor muscle exercises (PFME), and provide psychological support to make the process more manageable (Milios et al., 2019; Tosunöz et al., 2018; Wang et al., 2018). PFME is an effective method that stands out in the rehabilitation of incontinence after RP, and it is one of the most common practices aimed at increasing the strength of the pelvic floor muscles to eliminate sphincter weakness (Castellan et al., 2023; Chitre and Kulkarni, 2023; Pratiwi et al., 2020). Studies on the effectiveness of PFME indicate that these exercises can improve patients' urinary control (Azal et al., 2022). Nurses play a significant role in promoting pelvic floor muscle health by providing information and implementing educational programs and practices to ensure that these exercises are taught and performed correctly (Jalalinia et al., 2020; Storås et al., 2020).\n\nThis study aims to evaluate the effects of preoperative and postoperative nursing interventions on urinary incontinence management and quality of life in patients who have undergone RP. In this context, the effects of nursing interventions (education, pelvic floor muscle exercises, bladder training, etc.) on urinary incontinence severity, quality of life, and patient satisfaction will be examined comparatively. The study aims to identify the most effective nursing interventions in the management of urinary incontinence after RP and to integrate these interventions into clinical practice.",[78,79],"Prostate Cancer (Post Prostatectomy)","Urinary Incontinence (UI)","NOT_YET_RECRUITING","2026-05-21",{"date":83,"type":32},"2026-05-26",{"date":81,"type":21},{"date":81,"type":21},{"name":38,"class":39},{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":92,"acronym":4,"eligibilityCriteria":93,"healthyVolunteers":48,"sex":94,"minAge":17,"maxAge":71,"enrollmentInfo":95,"targetDuration":4,"studyType":22,"phases":97,"briefSummary":98,"conditions":99,"keywords":105,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":40},"100634646","effects-of-midwife-guided-birth-affirmation-cards-on-labor-process-and-experience-n-primigravidas-100634646","NCT07542392","Effects of Midwife-guided biırth Affirmation Cards on Labor Process and Experience ın Primigravidas","Effect of Midwife-Guided Birth Affirmation Cards on Labor Duration, Pain, Fear, Control and Perceived Support in Primigravidas: A Randomized Controlled Study","Inclusion Criteria:\n\n* Having a singleton pregnancy between 37-42 weeks of gestation\n* Being between 18-40 years of age\n* Being a primigravida\n* Having a cephalic presentation with vertex position\n* Being in the active phase of labor (cervical dilatation ≥4 cm)\n* Accepting non-invasive interventions\n* Having no mental or physical disability\n* Being able to understand and speak Turkish\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* High-risk pregnancies\n* Pregnant women at risk of intrapartum complications (e.g., oligohydramnios, polyhydramnios, intrauterine fetal demise, placenta previa, placental abruption, acute fetal distress, preeclampsia, fetal dystocia, macrosomia, etc.)\n* Pregnant women with a history of medical or obstetric complications\n* Women who have attended antenatal education classes (pregnancy school)\n* Women using epidural analgesia or other pharmacological pain management methods\n* Women experiencing communication difficulties\n* Women who are unwilling to participate in the study Exclusion Criteria from the Study\n* Experiencing dizziness, shortness of breath, or other discomfort,\n* Difficult and prolonged labor, instrumental delivery, placental retention, postpartum hemorrhage, need for neonatal intensive care,\n* Situations requiring emergency cesarean section during labor,\n* The woman will be excluded from the study if she ceases to cooperate during labor.","FEMALE",{"count":96,"type":21},60,[24],"The aim of this study is to evaluate the effects of midwife-guided birth affirmation cards on labor duration, pain level, fear of childbirth, perceived control, and perceived support in primigravidas. The study seeks to determine whether this non-pharmacological approach used during labor improves the childbirth experience. Accordingly, the research aims to answer the question: \"Do midwife-guided birth affirmation cards affect labor duration and the childbirth experience, including pain, fear, perceived control, and perceived support, in primigravidas?\"",[100,101,102,103,104],"Duration of Labor","Labor Pain","Fear of Childbirth","Control (Internet Only)","Support",[106,107,108,109,110,111,112,113],"Affirmation cards","labor pain","fear of childbirth","perceived control","perceived support","midwifery care","primigravida","non-pharmacological methods","2026-05-18",{"date":116,"type":32},"2026-05-19",{"date":118,"type":32},"2026-03-27",{"date":120,"type":21},"2026-08-31",{"name":38,"class":39},{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":127,"acronym":4,"eligibilityCriteria":128,"healthyVolunteers":48,"sex":94,"minAge":71,"maxAge":129,"enrollmentInfo":130,"targetDuration":4,"studyType":22,"phases":132,"briefSummary":133,"conditions":134,"keywords":138,"overallStatus":80,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":143,"startDateStruct":144,"completionDateStruct":146,"leadSponsor":148,"locationsCount":4},"100619459","mbsr-effects-on-aging-anxiety-and-body-image-100619459","NCT07344896","MBSR Effects on Aging Anxiety and Body Image","Effects of a Mindfulness-Based Stress Reduction Program on Aging Anxiety and Body Image in Middle-Aged Women: A Randomized Controlled Trial","Inclusion Criteria:\n\n* At least primary school graduate,\n* Being between 40-59 years old,\n* Living in Çumra district center,\n* Being open to communication and cooperation\n\nExclusion Criteria:\n\n* Those with chronic illnesses (self-report)\n* Foreign nationals Those with psychiatric illnesses (self-report) Those with physical disabilities and limited mobility","59 Years",{"count":131,"type":21},58,[24],"This study was designed to determine the effect of a mindfulness-based stress reduction (MBSR) program on aging anxiety and body image among middle-aged women. The primary hypotheses to be tested are as follows:\n\nH0a: There is no difference in the mean scores of the Aging Anxiety Scale between the women in the experimental group who receive the mindfulness-based stress reduction program and the women in the control group.\n\nH0b: There is no difference in the mean scores of the Body Image Scale between the women in the experimental group who receive the mindfulness-based stress reduction program and the women in the control group.\n\nH0c: There is no difference between the pre-intervention and post-intervention mean scores of the Aging Anxiety Scale among the women in the experimental group who receive the mindfulness-based stress reduction program.\n\nH0d: There is no difference between the pre-intervention and post-intervention mean scores of the Body Image Scale among the women in the experimental group who receive the mindfulness-based stress reduction program.\n\nThe researchers will compare the experimental group with the control group in order to assess the effect of the mindfulness-based stress reduction program on aging anxiety and body image among middle-aged women.\n\nParticipants:\n\n* They will attend an 8-session mindfulness-based stress reduction program.\n* They will participate in one silent mindfulness retreat session.",[135,136,137],"Body Image","Mindfulness Based Stress Reduction","Middle Aged",[139,140,141,142],"aging anxiety","middle age woman","mindfulness","body image",{"date":116,"type":32},{"date":145,"type":21},"2026-06-01",{"date":147,"type":21},"2027-05-30",{"name":38,"class":39},{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":153,"acronym":4,"eligibilityCriteria":154,"healthyVolunteers":11,"sex":94,"minAge":17,"maxAge":155,"enrollmentInfo":156,"targetDuration":4,"studyType":22,"phases":157,"briefSummary":158,"conditions":159,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":161,"lastUpdatePostDateStruct":162,"startDateStruct":164,"completionDateStruct":166,"leadSponsor":168,"locationsCount":40},"100632673","acute-effects-of-motor-imagery-exercises-in-individuals-with-pregnancy-related-lumbopelvic-pain-100632673","NCT07516743","Acute Effects of Motor Imagery Exercises in Individuals With Pregnancy-Related Lumbopelvic Pain","Inclusion Criteria:\n\n* Be in a singleton, uncomplicated pregnancy.\n* Lumbopelvic pain (lower back or pelvic girdle pain) must have begun during pregnancy.\n* Be between the 12th and 40th weeks of pregnancy.\n* Be capable of understanding motor imagery training and following instructions.\n\nExclusion Criteria:\n\n* A history of chronic lower back pain present before pregnancy and persisting during pregnancy.\n* Symptoms of neuropathic lower back pain (e.g., radiculopathy), inflammatory conditions such as tumors, infections, compression fractures, or ankylosing spondylitis that are specific causes of lower back or pelvic pain, a history of previous spinal or pelvic surgery,\n* Severe neurological disorders, metabolic disorders, or severe orthopedic conditions,\n* Medical restrictions that prevent exercise or maintaining certain positions (e.g., lying on the back).","45 Years",{"count":20,"type":21},[24],"The aim of this study is to investigate the effects of single-session motor imagery exercises on pain and motor imagery in individuals with pregnancy-related lumbopelvic pain.",[160],"Pregnancy-related Lumbopelvic Pain","2026-04-08",{"date":163,"type":32},"2026-04-13",{"date":165,"type":32},"2026-04-01",{"date":167,"type":21},"2026-08-02",{"name":38,"class":39},{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":175,"eligibilityCriteria":176,"healthyVolunteers":48,"sex":16,"minAge":177,"maxAge":178,"enrollmentInfo":179,"targetDuration":4,"studyType":22,"phases":181,"briefSummary":182,"conditions":183,"keywords":185,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":40},"100627331","parent-education-about-human-papillomavirus-hpv-100627331","NCT07447245","Parent Education About Human Papillomavirus (HPV)","The Effect of Parent Education on Human Papillomavirus Vaccination Intention: A Randomized Controlled Trial","(HPV)","Inclusion Criteria:\n\n* Parent must be between 18-49 years old\n* Parent must be a child aged 11-18\n* Parent must not have hearing or speech problems\n* Parent must be able to read and write in Turkish\n* Parent must agree to participate in the study\n\nExclusion Criteria:\n\n• Parents of children who have received the HPV vaccine","11 Years","49 Years",{"count":180,"type":21},52,[24],"Human papillomavirus (HPV) is the most common sexually transmitted infection worldwide and is the primary cause of cervical cancer. According to World Health Organization (WHO) systems, there were approximately 660,000 new cases of cervical cancer and 350,000 deaths in 2022. In Turkey, the prevalence of cervical cancer was reported as 8,761 in the last five years. HPV vaccines are safe and effective in preventing HPV transmission and cancer and are included in 147 national immunization programs; However, they have not yet been included in the national immunization program in Turkey. The WHO has reissued a regional strategy to eliminate cervical cancer by 2030, which includes vaccinating 90% of girls by age 15, screening 70% of women between the ages of 35 and 45, and increasing the treatment of 90% of precancerous lesions and invasive cervical cancer. The HPV vaccine provides the highest protection before the onset of sexual activity, and ACIP recommends routine vaccination of all 11-12-year-olds (starting at age 9). Catch-up vaccination is recommended for individuals up to age 26 who have not been previously vaccinated. Gardasil and Cervarix vaccines have been licensed in Turkey since 2007; However, vaccination rates are limited by the vaccine not being covered by social security, its cost, the number of doses, and low parental awareness. The safety of HPV vaccines is regularly monitored by international organizations, with approximately 1.7 cases of anaphylaxis per million doses administered.",[184],"HPV (Human Papillomavirus)-Associated",[186,187,188,189],"HPV","vaccine","patern","education","2026-02-27",{"date":192,"type":32},"2026-03-03",{"date":194,"type":21},"2026-02-15",{"date":196,"type":21},"2026-12-15",{"name":38,"class":39},{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":4,"eligibilityCriteria":204,"healthyVolunteers":11,"sex":16,"minAge":205,"maxAge":206,"enrollmentInfo":207,"targetDuration":4,"studyType":22,"phases":208,"briefSummary":209,"conditions":210,"keywords":212,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":222,"locationsCount":40},"100624443","gamification-intervertion-in-children-with-type-1-diabetes-100624443","NCT07409701","Gamification Intervertion in Children With Type 1 Diabetes","The Effect of Education Provided to Children With Type 1 Diabetes Using Gamification Methods on Health Literacy and Quality of Life: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Diagnosed with type 1 diabetes\n* Aged between 8 and 12 years\n* Diagnosed with type 1 diabetes for at least 1 year and having received standard diabetes education\n* Able to read and write\n\nExclusion Criteria:\n\n* Presence of speech, hearing, or visual impairments\n* Presence of any other comorbid chronic disease\n* Presence of cognitive impairment","8 Years","12 Years",{"count":180,"type":21},[24],"Objective: This study aims to examine the effect of education provided through gamification methods on health literacy and quality of life in children diagnosed with type 1 diabetes (T1DM).\n\nMaterials and Methods: The study is planned as a randomized controlled trial with a pre-test-post-test, parallel design (1:1). The data for the study will be collected between January and April 2026 from patients diagnosed with type 1 diabetes mellitus at the Ankara Etlik City Hospital Pediatric-2 Endocrinology Service. The sample size has been determined to be 52 patients, with 26 in each of the experimental and control groups, based on data from similar studies in the literature. Data will be collected through individual interviews using a Personal Information Form, the Health Literacy Scale for Acute Complications of Diabetes in Children Aged 8-12 with type 1 diabetes mellitus, and the Quality of Life Scale for Children with Diabetes Mellitus. The gamified education will be provided by a researcher who has completed a 2.5-hour training program from BTK Academy. Informed Consent Forms and other forms will be completed by patients who meet the inclusion criteria and volunteer to participate. Randomization will be performed by someone other than the researcher. The experimental group will receive gamified education in addition to standard education, while the control group will receive only standard education. Data will be analyzed using the SPSS program. The research will be conducted in accordance with the principles of the Helsinki Declaration.\n\nFindings: The findings of the study will be analyzed using SPSS after the application and data collection are completed.\n\nConclusion: The results of the study will be written after the application of the study and the collection of data, followed by the analysis of the data using SPSS and the determination of the findings.",[211],"Type 1 Diabetes Mellitus",[211,213,214,215],"Gamification","Health literacy","Quality of life","2026-02-06",{"date":218,"type":32},"2026-02-13",{"date":220,"type":21},"2026-01-25",{"date":61,"type":21},{"name":38,"class":39},{"id":224,"slug":225,"hasResults":11,"nctId":226,"briefTitle":227,"officialTitle":228,"acronym":4,"eligibilityCriteria":229,"healthyVolunteers":48,"sex":94,"minAge":17,"maxAge":230,"enrollmentInfo":231,"targetDuration":4,"studyType":22,"phases":232,"briefSummary":233,"conditions":234,"keywords":238,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":243,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":249,"locationsCount":40},"100621369","effects-of-mobilization-and-caffeine-after-cesarean-100621369","NCT07369726","Effects of Mobilization and Caffeine After Cesarean","The Effect of Early Post-Cesarean Mobilization and Caffeine Consumption on Bowel Motility, Pain, and Psychological Well-being: A Randomized Controlled Trial","Inclusion Criteria:\n\n1. Being between 18 and 35 years of age,\n2. Women who underwent cesarean delivery under spinal anesthesia,\n3. Having a post-cesarean pain level of 4 or higher,\n4. Being able to understand and write Turkish and communicate effectively with researchers.\n\nExclusion Criteria:\n\n1. Women who underwent emergency cesarean delivery,\n2. Those with pregnancy complications (preeclampsia, placenta previa, etc.),\n3. Those with a history of chronic gastrointestinal disease (e.g., irritable bowel syndrome, Crohn's disease, ulcerative colitis),\n4. Those with sensitivity or allergy to caffeine,\n5. Those with a history of chronic pain syndrome or dependence on analgesics,\n6. Regular coffee drinkers (≥2 cups per day),\n7. Intraoperative complications such as bowel or bladder injury,\n\ni) Those who cannot comply with the study protocol or complete the follow-up process.\n\nRemoval Criteria:\n\n1. Participants are excluded from the study under the following conditions:\n2. During surgery If complications occur (e.g., bladder or bowel injury, excessive bleeding),\n3. Postoperative complications requiring admission to the intensive care unit (ICU) for the mother or newborn,\n4. Development of severe postoperative nausea, vomiting, or intolerance to oral intake,\n5. Inability to consume or refusal to consume coffee according to the study protocol,\n6. Withdrawal of consent by the participant at any point during the study,\n7. Failure to comply with surgical procedures or loss of follow-up,\n8. Development of medical conditions during follow-up that may affect study results (e.g., acute infections, neurological disorders).","35 Years",{"count":96,"type":21},[24],"This study Maims to assess bowel motility, pain and psychological well-being in women in the post-cesarean period by mobilizing them early and encouraging them to consume coffee.",[235,236,237],"Gastrointestinal Motility","Postoperative Pain","Psychological Well-Being",[239,240,237,241],"gastrointestinal motility","postoperatif pain","Early Ambulation","2026-02-05",{"date":244,"type":32},"2026-02-09",{"date":246,"type":32},"2025-11-25",{"date":248,"type":21},"2026-05-01",{"name":38,"class":39},{"id":251,"slug":252,"hasResults":11,"nctId":253,"briefTitle":254,"officialTitle":255,"acronym":4,"eligibilityCriteria":256,"healthyVolunteers":48,"sex":94,"minAge":17,"maxAge":230,"enrollmentInfo":257,"targetDuration":4,"studyType":22,"phases":259,"briefSummary":260,"conditions":261,"keywords":262,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":267,"startDateStruct":268,"completionDateStruct":269,"leadSponsor":270,"locationsCount":40},"100618260","post-caesarean-pranayama-and-pain-100618260","NCT07329309","Post-Caesarean Pranayama and Pain","The Effect of Post-Caesarean Section Pranayama Breathing Exercises on Pain and Postpartum Comfort: A Randomised Controlled Trial","Inclusion Criteria:\n\n* Undergone a caesarean section under spinal anaesthesia\n* Reported a post-operative pain level of at least 4 on the Numerical Rating Scale (NRS)\n* Knowledge of Turkish\n* Ability to communicate effectively with the research team\n* Volunteer to participate in the study and provide written consent\n\nExclusion Criteria:\n\n* Having given birth by emergency caesarean section\n* Presence of pregnancy complications (e.g. pre-eclampsia, gestational diabetes, placenta praevia)\n* History of chronic pain or analgesic dependence\n* Requirement for admission to the intensive care unit in the early postoperative period\n* Need for additional surgical intervention\n* Development of significant intraoperative or postoperative complications\n* Refusal to exercise or intolerance to exercise\n* Failure to comply with study procedures\n* Withdrawal of consent\n* Incomplete follow-up\n* Development of a new medical condition during the study that could affect the results",{"count":258,"type":21},100,[24],"This study aims to investigate the effect of pranayama breathing exercises on postoperative pain and postpartum comfort levels in women following caesarean section, with the objective of providing important evidence for the integration of non-pharmacological methods into postpartum care.",[236],[263,264,265,266],"caesarean section","pain","pranayama","comfort",{"date":244,"type":32},{"date":242,"type":32},{"date":163,"type":21},{"name":38,"class":39},{"id":272,"slug":273,"hasResults":11,"nctId":274,"briefTitle":275,"officialTitle":276,"acronym":4,"eligibilityCriteria":277,"healthyVolunteers":48,"sex":16,"minAge":278,"maxAge":279,"enrollmentInfo":280,"targetDuration":4,"studyType":22,"phases":282,"briefSummary":283,"conditions":284,"keywords":290,"overallStatus":80,"whyStopped":4,"lastUpdateSubmitDate":292,"lastUpdatePostDateStruct":293,"startDateStruct":295,"completionDateStruct":297,"leadSponsor":299,"locationsCount":4},"100550129","the-effect-of-virtual-reality-and-buzzy-application-on-pain-fear-and-anxiety-during-prick-test-in-children-100550129","NCT06443060","The Effect of Virtual Reality and Buzzy Application on Pain, Fear and Anxiety During Prick Test in Children","The Effect of Virtual Reality and Buzzy Application on Pain, Fear and Anxiety During Prick Test in Children: Randomized Controlled Study","Inclusion Criteria:\n\n* The child must be between the ages of 7-10\n* It will be the first time that a prick test will be applied.\n* The child can speak and understand Turkish comfortably\n* He and his family agree to participate in the study.\n* Not having used analgesic medication at least six hours ago\n\nExclusion Criteria:\n\n* The child has any diagnosed psychiatric disorder\n* Having visual, auditory or speech disorders\n* Having a chronic disease other than allergy","7 Years","10 Years",{"count":281,"type":21},111,[24],"Allergy is a hypersensitivity reaction to a triggering agent. Tests used in allergy are divided into two: in vivo and in vitro. Among the in vivo tests routinely used, epidermal, intradermal and patch tests are used, and the most commonly used is the skin prick test. In order to prevent the negative effects of pain, it is important to be informed about the appropriate approach to children, newborns and babies, and effective pain management, according to their cognitive development levels. Pain management in children should be done appropriately with accurate assessment tools. This will increase the quality of life, reduce hospitalizations, shorten the length of hospital stay and reduce costs. Pain experiences experienced during childhood will cause later pain experiences to be perceived as more severe and cause anxiety and fear. Anxiety is a psychological, physiological and behavioral state that develops in response to a perceived or existing threat. Anxiety, which can also be expressed as worry or anxiety, is a emotional state that can occur in various ways, such as restlessness, tension, easy fatigue, lack of concentration, muscle tension, and sleep disturbance, in which autonomic and somatic symptoms occur in the body, without any reason.\n\nVirtual reality provides multi-sensory information as children focus on the simulated world. Virtual reality, one of the cognitive methods; It can create an environment where three-dimensional pictures or animations created on the computer can interact in people's minds. It is also defined as a distraction method created by software, which creates the feeling that users are in the environment even though they are not in the real environment, and can interact with people in the environment. When all these studies were examined, no three-group study was found comparing a distracting method with a physical method for the 7-10 age group. Additionally, there is a study that used virtual reality in the prick test, but there is no method that has been proven to be superior to virtual reality. In this study, it will be investigated whether virtual reality and buzzy applications have a reducing effect on pain, fear and anxiety compared to the control group. Virtual reality and buzzy techniques will also be compared with each other. Since no such study has been found in the literature, it is thought to contribute to the field.",[285,286,287,288,289],"Pain","Fear","Anxiety","Children, Only","Virtual Reality",[291,289,285,286,287],"BUZZY","2025-09-11",{"date":294,"type":32},"2025-09-17",{"date":296,"type":21},"2025-10-15",{"date":298,"type":21},"2025-12-15",{"name":38,"class":39},{"id":301,"slug":302,"hasResults":11,"nctId":303,"briefTitle":304,"officialTitle":305,"acronym":306,"eligibilityCriteria":307,"healthyVolunteers":48,"sex":94,"minAge":17,"maxAge":71,"enrollmentInfo":308,"targetDuration":4,"studyType":22,"phases":310,"briefSummary":311,"conditions":312,"keywords":318,"overallStatus":80,"whyStopped":4,"lastUpdateSubmitDate":324,"lastUpdatePostDateStruct":325,"startDateStruct":327,"completionDateStruct":329,"leadSponsor":331,"locationsCount":40},"100565313","the-effect-ofgreen-future-with-midwife-handsclimate-change-animation-on-mothers-climate-change-awareness-and-behavior-100565313","NCT06640556","The Effect of\"Green Future With Midwife Hands\"Climate Change Animation on Mothers' Climate Change Awareness and Behavior","The Effect of \"Green Future With Midwife Hands\" Climate Change Animation on Mothers' Climate Change Awareness and Behavior","RKÇ","Inclu• Pregnant women who can read and write Turkish,\n\n* Volunteer to participate in the research,\n* Have had a normal or cesarean delivery,\n* Are primiparous,\n* Are open to communication (able to understand and answer questions) will be included in the samplesion Criteria:\n\nExclusion Criteria:\n\n* • Those who do not have the ability to read, listen, write, speak and understand Turkish,\n\n  * Those who have hearing or visual impairments,\n  * Those who have postpartum complications,\n  * Those who have had a stillbirth,\n  * Those who wish to withdraw from the study were not included.",{"count":309,"type":21},666,[24],"The Effect of \"Green Future with Midwife Hands\" Climate Change Animation on Mothers' Climate Change Awareness and Behavior Climate change appears as one of the most important environmental problems of today. Many negative effects such as the increase in greenhouse gas emissions, global warming, sea level rise and the frequency of extreme weather events threaten both natural ecosystems and human life. In this context, it is of great importance for individuals to gain awareness about climate change and exhibit environmentally friendly behavior for a sustainable future. In particular, mothers and expectant mothers have the potential to create significant awareness and change by choosing products that do not harm the environment, while looking for the best for their babies. Reducing plastic use, choosing organic textile products, using biodegradable wet wipes and choosing toys made from natural materials both protect babies' health and support environmental sustainability. This awareness reinforces the environmentally friendly behavior of mothers and helps future generations grow up as more conscious individuals. The role of mothers in this regard is undeniably great for a sustainable future. While mothers making environmentally friendly choices increases the environmental awareness of not only their own families but also the wider masses, being careful when choosing carbon footprint baby products both protects the health of babies and reduces environmental impacts.\n\nThis research aims to encourage mothers and expectant mothers to make environmentally friendly and carbon footprint-reducing choices when choosing baby products by increasing the climate change awareness of mothers and expectant mothers through the \"Green Future with Midwife Hands\" Climate Change Animation.",[313,314,315,316,317],"Climate Change","Awareness","Conscious","Consumption","Consumption Habits of Mothers",[319,320,321,322,323],"Climate change","awareness","conscious","consumption","consumption habits of mothers","2025-09-09",{"date":326,"type":32},"2025-09-15",{"date":328,"type":21},"2025-09-10",{"date":330,"type":21},"2025-10-01",{"name":38,"class":39},{"id":333,"slug":334,"hasResults":11,"nctId":335,"briefTitle":336,"officialTitle":336,"acronym":337,"eligibilityCriteria":338,"healthyVolunteers":48,"sex":94,"minAge":4,"maxAge":4,"enrollmentInfo":339,"targetDuration":4,"studyType":22,"phases":341,"briefSummary":342,"conditions":343,"keywords":348,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":350,"lastUpdatePostDateStruct":351,"startDateStruct":352,"completionDateStruct":354,"leadSponsor":356,"locationsCount":40},"100597000","development-and-effectiveness-evaluation-of-a-clustered-care-guideline-within-individualized-developmental-care-rct-100597000","NCT07052786","Development and Effectiveness Evaluation of a Clustered Care Guideline Within Individualized Developmental Care: RCT","Guideline","Inclusion Criteria:\n\n* Working in the NICU of Necmettin Erbakan University Medical Faculty Hospital,\n\n  * Having at least 3 months of experience in the NICU,\n  * Volunteering to participate in the research.\n\nExclusion Criteria:\n\n* The nurse wanting to leave the study during the study\n\n  * The nurse not participating in the training or not completing the training\n  * The nurse not being able to complete the study, including the final",{"count":340,"type":21},44,[24],"The Individualized Developmental Care (IDC) model was developed to minimize the negative impact of the neonatal intensive care environment and to support infants' physiological stability. It supports the practice of clustered care, which refers to grouping routine medical and nursing procedures into a single care time period to reduce handling and allow the infant uninterrupted rest and maintenance of the sleep-wake cycle.\n\nThis study aims to develop a clustered care practice guideline and evaluate its effectiveness. The study was designed as a single-blind randomized controlled trial, where the participating nurses will not be informed about their group allocation (intervention or control) to reduce bias.The study will be conducted between July and September 2025 in the level 2 and 3 NICUs of Necmettin Erbakan University Faculty of Medicine Hospital in Konya, Turkey.\n\nThe study population includes all 44 nurses working in these NICUs who meet the inclusion criteria and agree to participate. Since the entire population is accessible, total population sampling will be used. After data collection is completed, a post hoc power analysis will be conducted using G\\*Power (v3.1.9.2).\n\nData will be collected using the \"Descriptive Information Form for the Infant and the Nurse\" and the \"Clustered Care Practice Guideline\". Pre-test data will be collected before training, and post-test data will be collected 4-6 weeks after the training.\n\nThe intervention group will receive the Clustered Care Practice Training Based on Individualized Developmental Care in two in-person sessions (approx. 45 minutes per session), delivered in small groups (11-12 participants). A training booklet prepared by the researchers will be distributed at the end of the sessions.\n\nThe normality of the data will be assessed using the Kolmogorov-Smirnov test, normal distribution curves, and skewness-kurtosis values. Parametric tests will be used for normally distributed data; non-parametric tests will be used otherwise. A significance level of P\\\u003C0.05 will be applied.\n\nEthical approval was obtained from the Ethics Committee of KTO Karatay University Pharmaceutical and Medical Research (decision no: 2022\u002F014, date: 21.06.2022). Institutional permission was obtained from NEU Faculty of Medicine Hospital. Written informed consent will be obtained from all participating nurses and from parents of the observed infants.",[344,345,346,347],"Premature Infant","Clustered Care","Neonatal Intensive Care Unit","Developmental Care",[349],"clustered care, guideline,nurse, NICU","2025-09-08",{"date":326,"type":32},{"date":353,"type":32},"2025-07-01",{"date":355,"type":21},"2025-12-30",{"name":38,"class":39},{"id":358,"slug":359,"hasResults":11,"nctId":360,"briefTitle":361,"officialTitle":362,"acronym":4,"eligibilityCriteria":363,"healthyVolunteers":48,"sex":16,"minAge":364,"maxAge":365,"enrollmentInfo":366,"targetDuration":4,"studyType":22,"phases":367,"briefSummary":368,"conditions":369,"keywords":371,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":378,"lastUpdatePostDateStruct":379,"startDateStruct":381,"completionDateStruct":383,"leadSponsor":384,"locationsCount":40},"100598349","neuroathletic-exercise-in-the-elderly-100598349","NCT07070336","Neuroathletic Exercise In The Elderly","The Effect Of Neuroathletic Exercise On Walking Speed, Fall Risk And Cognitive Functions In The Elderly","Inclusion Criteria:\n\n* Ages between 60-80\n* Volunteering to participate in the study\n* Having the ability to perform physical, cognitive and sensory tests and exercises\n\nExclusion Criteria:\n\n* Having a history of injury to the lower and upper extremities within the last year\n* Having regular physical activity or sports habits.\n* Having participated in any physical activity program in the last 6 months\n* Having a sensory pathology that prevents participation in the study\n* Having any musculoskeletal, neurological, respiratory or cardiovascular pathology that will limit exercise\n* Having a history of malignant disease\n* Having an eye defect that cannot be corrected with lenses, such as cataracts, that prevents tests","60 Years","80 Years",{"count":20,"type":21},[24],"Objective: The aim of this protocol study was to investigate the effect of neuroathletic exercise on walking speed, fall risk and cognitive function in the elderly.\n\nMethod: The study is planned as a single-centre, double-blind, parallel group randomised controlled experimental design and will be conducted in accordance with SPIRIT. The sample of the study will consist of healthy elderly people aged 60-80 years. In order to ensure parametric conditions, the sample will be divided into two groups as experimental group (n=30) in which neuroathletic exercise will be performed and control group (n=30) in which Turkey Physical Activity Guidelines will be given and a total of 60 elderly people will be randomly assigned to the groups. The elderly assigned to the experimental and control groups according to the order of randomisation will be administered the timed up and go test (TUG), short physical performance battery (SPPB), geriatric depression scale (GDÖ), MoCA test as pre-test and post-test. The experimental group will be asked to perform neuroathletic exercises two days a week for 12 weeks under the supervision of a physiotherapist, and will be asked to perform a home exercise programme one day a week. The control group will be given the Turkish Physical Activity guide. Data will be collected by the researcher.\n\nResults: Considering the limited number of studies on the use of neuroathletic exercises in the literature, it is thought that our randomised controlled study designed to determine the effect of neuroathletic exercise on walking speed, fall risk and cognitive functions in the elderly will contribute to the literature.",[370],"Healthy Aging",[372,373,374,375,376,377],"aging","neuroathletic exercise","walking speed","gait speed","fall risk","cognitive function","2025-09-01",{"date":380,"type":32},"2025-09-04",{"date":382,"type":32},"2025-05-01",{"date":248,"type":21},{"name":38,"class":39},{"id":386,"slug":387,"hasResults":11,"nctId":388,"briefTitle":389,"officialTitle":390,"acronym":4,"eligibilityCriteria":391,"healthyVolunteers":48,"sex":94,"minAge":4,"maxAge":4,"enrollmentInfo":392,"targetDuration":4,"studyType":22,"phases":394,"briefSummary":395,"conditions":396,"keywords":401,"overallStatus":80,"whyStopped":4,"lastUpdateSubmitDate":403,"lastUpdatePostDateStruct":404,"startDateStruct":406,"completionDateStruct":407,"leadSponsor":409,"locationsCount":4},"100554949","postnatal-companion-support-the-effect-of-education-on-maternal-depression-and-fatigue-100554949","NCT06505733","Postnatal Companion Support The Effect of Education on Maternal Depression and Fatigue","Postnatal Companion Support The Effect of Education on Maternal Depression and Fatigue: A Randomised Controlled Trial","Inclusion Criteria:\n\n* Knowing how to read and write Turkish,\n* Volunteer to participate in the research,\n* She gave birth by cesarean section,\n* Primiparous,\n* Pregnant women who are open to communication (able to understand and answer questions) will be included in the sample.\n\nExclusion Criteria:\n\n* Those who do not have the skills of reading, listening, writing, speaking and understanding Turkish,\n* Those who have a hearing or visual impairment,\n* Having postpartum complications,\n* giving birth to stillbirth,\n* People who wanted to withdraw from the study were not included.",{"count":393,"type":21},72,[24],"In this study, it is aimed to investigate the effect of the trainings included in the content of the practical guide for postpartum supporter training companions, which will be given to the companions of women in the postpartum period, on depression and fatigue on mothers. The research will be conducted in methodological and single blind randomised control design. The study will be conducted at Necmettin Erbakan University Faculty of Medicine Hospital. A total of 70 puerperants will be included in the study as intervention (n: 35) and control (n: 35) groups. Introductory Information Form, Postpartum depression rating scale as data collection tools in the study: Motherhood Monitoring Scale by Parents (MMSP), Edinburgh Postnatal Depression Scale (EDDS), Multidimensional Fatigue Rating Scale will be used. The research data will be collected three times as pre-test data, fourth day and tenth day. Number, percentage, mean and standard deviation will be used in the evaluation of descriptive data; Chi-square test will be used for the similarity of the descriptive characteristics of the experimental and control groups; Kolmogrow-Smirnov and Shapiro-Wilk will be used in the normality analysis of dependent variables; t test in independent groups (student t test) will be used to compare the post-test scores of the experimental and control groups; and ANOVA in dependent groups will be used to compare the pre-test-post-test mean scores of the experimental group and eta square will be used to calculate effect sizes. The results obtained will be tested at p\\\u003C0.05 significance level and bidirectionally. When the literature is examined, there is not enough data on the depression and fatigue of the companion caring for the woman in the postpartum period. This study aims to fill the gaps in the literature and to reduce depression and fatigue in mothers.",[397,398,399,400],"Postpartum","Fatigue","Depression","Social Support",[402,399,398,397],"social support","2024-08-07",{"date":405,"type":32},"2024-08-09",{"date":403,"type":21},{"date":408,"type":21},"2024-08-17",{"name":38,"class":39},{"id":411,"slug":412,"hasResults":11,"nctId":413,"briefTitle":414,"officialTitle":415,"acronym":4,"eligibilityCriteria":416,"healthyVolunteers":48,"sex":94,"minAge":17,"maxAge":230,"enrollmentInfo":417,"targetDuration":4,"studyType":22,"phases":418,"briefSummary":419,"conditions":420,"keywords":422,"overallStatus":80,"whyStopped":4,"lastUpdateSubmitDate":425,"lastUpdatePostDateStruct":426,"startDateStruct":428,"completionDateStruct":430,"leadSponsor":432,"locationsCount":4},"100456402","aloe-vera-on-caesarean-section-wound-100456402","NCT05223127","Aloe Vera on Caesarean Section Wound","Effect of Aloe Vera on Caesarean Section Wound Healing: Randomized Controlled Study","Inclusion Criteria:\n\n* In the age range of 18-35,\n* Primiparous,\n* Gestational week 37 and above,\n* Transver incision made,\n* Women who volunteered to participate in the study\n\nExclusion Criteria:\n\n* Body mass index not in the range of 18.5-24.9,\n* Having pregnancy complications (such as preeclampsia and diabetes),\n* Having chronic diseases (such as anemia, coagulopathy, cardiovascular diseases and respiratory and kidney diseases),\n* Smoking or substance use,\n* Those who use drugs that affect wound healing (glucocorticoids, anticoagulants, immunosuppressants, antibiotics and chemotherapy drugs before cesarean section),\n* Postpartum fever (≥38 ◦C),\n* Conditions that cause excessive stretching of the uterus (multiple pregnancy, polyhydramnios),\n* Self or baby in need of intensive care,\n* Having had a hysterectomy or myomectomy during the operation,\n* The operation takes more than 90 minutes,\n* Individuals who do not want to withdraw from the study",{"count":96,"type":21},[24],"Conducting clinical research in line with the literature recommendation, with a method that is low-cost, accessible, easy-to-use, and examined in an evidence-based design related to cesarean section wound, which negatively affects the quality of life of women in the postpartum period, constitutes the original value and our main motivation of the project.",[421],"Cesarean Section",[423,421,424],"Aloe","Wound Healing","2023-11-13",{"date":427,"type":32},"2023-11-14",{"date":429,"type":21},"2024-08-01",{"date":431,"type":21},"2026-10-30",{"name":38,"class":39},""]