[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Uskudar University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":610},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,36,0,25,[9,42,70,99,128,148,176,198,217,245,266,283,302,317,344,370,392,414,431,462,487,525,546,565,593],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100645151","the-mediating-role-of-balance-in-the-relationship-between-fatigue-and-fear-of-falling-in-individuals-with-multiple-sclerosis-100645151",false,"NCT07680049","The Mediating Role of Balance in the Relationship Between Fatigue and Fear of Falling in Individuals With Multiple Sclerosis","Inclusion Criteria:\n\n* Age 18-65 years\n* Neurologist-confirmed MS diagnosis\n* No relapse within the previous 30 days\n* Ability to walk independently or with an assistive device\n* Ability to understand instructions\n* Voluntary participation\n\nExclusion Criteria:\n\n* Recent MS relapse\n* Severe vestibular disorder\n* Other neurological diseases\n* Severe orthopedic conditions affecting mobility\n* Recent lower extremity surgery or trauma\n* Cardiopulmonary conditions limiting assessment","ALL","18 Years","75 Years",{"count":20,"type":21},40,"ESTIMATED","OBSERVATIONAL","Fatigue, balance impairment, and fear of falling are common problems in individuals with Multiple Sclerosis (MS). Previous studies have shown significant associations among these variables; however, the mechanisms underlying the relationship between fatigue and fear of falling remain unclear. It is possible that fatigue increases fear of falling indirectly through its negative effects on balance performance.",[25],"Multiple Sclerosis",[27,25,28,29],"Fatigue","Postural Balance","Fear","NOT_YET_RECRUITING","2026-06-25",{"date":33,"type":34},"2026-07-01","ACTUAL",{"date":33,"type":21},{"date":37,"type":21},"2026-07-25",{"name":39,"class":40},"Uskudar University","OTHER",1,{"id":43,"slug":44,"hasResults":12,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":59,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":69,"locationsCount":41},"100590009","the-effect-of-inspiratory-muscle-training-with-substance-use-disorder-100590009","NCT06961838","The Effect of Inspiratory Muscle Training With Substance Use Disorder","Inclusion Criteria:\n\n* Being older than 18 years\n\n  * Meeting the current Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria for Substance Use Disorder\n  * Receiving inpatient treatment\n  * Substance use for more than one year\n  * Being able to follow simple instructions\n  * Not having any visual and auditory pathology\n  * Being able to cooperate with the devices used.\n\nExclusion Criteria:\n\n* Failure to comply with the treatment and assessment program\n* Participation in a structured physiotherapy\u002Fexercise program in the last 6 months\n* Presence of current psychotic symptoms\n* Presence of any physical disability or medical problem\n* Presence of respiratory system problems such as asthma and tuberculosis and infectious health problems (e.g. HIV, hepatitis B).",{"count":49,"type":21},34,"INTERVENTIONAL",[52],"NA","The aim was to investigate the effectiveness of inspiratory muscle training on dyspnoea, pulmonary function, respiratory muscle strength, cough capacity, functional exercise capacity, substance craving, depression, anxiety and quality of life in individuals with substance use disorder.",[55,56,57,58],"Substance Abuse Disorder","Exercise","Pulmonary Function","Rehabilitation",[60,56,58,57,61],"Substance Use Disorder","Muscle Training","RECRUITING","2026-04-28",{"date":65,"type":34},"2026-05-05",{"date":67,"type":34},"2025-07-03",{"date":33,"type":21},{"name":39,"class":40},{"id":71,"slug":72,"hasResults":12,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":77,"sex":16,"minAge":17,"maxAge":78,"enrollmentInfo":79,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":81,"conditions":82,"keywords":85,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":41},"100622758","sleep-quality-and-cognitive-functions-in-adults-a-cross-sectional-study-100622758","NCT07387783","Sleep Quality and Cognitive Functions in Adults: A Cross-Sectional Study","The Association Between Sleep Quality and Cognitive Functions in Healthy Young Adults","Inclusion Criteria:\n\n* Between 18 and 35 years.\n* Ability and willingness to provide written informed consent.\n* Sufficient ability to read, understand, and communicate in Turkish, the language in which the assessments are administered.\n* Self-reported good general health, with no active medical or psychiatric conditions that significantly affect daily functioning.\n* Willingness and ability to wear a wearable sleep monitoring device continuously for five consecutive days and to comply with device usage instructions.\n* Ability to attend and complete a single-session cognitive assessment\n\nExclusion Criteria:\n\n* Regular or frequent use of medications known to affect sleep or cognitive function, including sedative-hypnotics, benzodiazepines, antipsychotics, stimulants, opioids, or similar agents.\n* Initiation of, or dose changes in, psychotropic medications within the past four weeks.\n* Being under the influence of alcohol or illicit substances on the day of cognitive testing.\n* Engagement in night shift work or rotating shift schedules within the past one month.\n* Travel across time zones resulting in a time difference of two hours or more within the past two weeks.\n* Uncontrolled high daily intake of caffeine (e.g., \\>400 mg\u002Fday) and unwillingness to reduce consumption during the study period.\n* Color blindness or other color vision deficiencies, due to their potential impact on Stroop Test performance.\n* Dermatological conditions, allergies, or skin lesions at the wrist that prevent wearing the device, or refusal to wear the device as required.\n* Acute illness within the past two weeks, including febrile infections, severe pain, or other acute medical conditions that may temporarily affect sleep or cognitive performance.\n* Pregnancy or early postpartum period.",true,"35 Years",{"count":80,"type":21},75,"This observational cross-sectional study aims to examine the association between sleep quality and cognitive functions in healthy young adults. Subjective sleep quality will be assessed using the Pittsburgh Sleep Quality Index, and objective sleep parameters will be collected using a wearable device over five consecutive days. Cognitive functions will be evaluated at a single assessment session using standardized neuropsychological tests, including measures of attention, executive functions, and verbal memory. The study seeks to explore relationships between subjective and objective sleep measures and cognitive performance. Findings from this study may contribute to a better understanding of how sleep quality is associated with cognitive functioning in healthy young adults.",[83,84],"Sleep Quality","Cognitive Functions",[86,87,88,89,90],"sleep quality","Cognitive Function","Young Adults","verbal memory","wearable device","2026-04-27",{"date":93,"type":34},"2026-04-29",{"date":95,"type":34},"2026-01-26",{"date":97,"type":21},"2026-08",{"name":39,"class":40},{"id":100,"slug":101,"hasResults":12,"nctId":102,"briefTitle":103,"officialTitle":104,"acronym":105,"eligibilityCriteria":106,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":107,"enrollmentInfo":108,"targetDuration":4,"studyType":50,"phases":110,"briefSummary":111,"conditions":112,"keywords":115,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":41},"100633237","effects-of-muscle-energy-technique-on-neck-disability-and-cervical-range-of-motion-in-individuals-with-non-specific-neck-pain-100633237","NCT07524075","Effects of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Individuals With Non-Specific Neck Pain","The Effect of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Patients With Non-Specific Neck Pain","MET-NP","Inclusion Criteria:\n\nAge between 18 and 65 years Diagnosis of non-specific neck pain Presence of neck pain for at least 4 weeks Ability to understand and follow instructions Willingness to participate in the study\n\nExclusion Criteria:\n\nHistory of cervical spine surgery Presence of neurological deficits or radiculopathy Specific causes of neck pain (e.g., tumor, infection, fracture) Severe cervical disc herniation Pregnancy Any contraindication to manual therapy","65 Years",{"count":109,"type":21},60,[52],"This study aims to investigate the effect of the Muscle Energy Technique on neck disability level and cervical range of motion in individuals with non-specific neck pain. The study will be conducted at Avicenna International Hospital in Istanbul. Participants with non-specific neck pain will be included in the study. The intervention will involve the application of Muscle Energy Technique, and outcomes will be assessed using standardized measures of neck disability and cervical range of motion. The findings are expected to contribute to improving treatment approaches for individuals with non-specific neck pain.",[113,114],"Non-specific Neck Pain","Neck Pain",[114,116,117,118,119],"Non-Specific Neck Pain","Muscle Energy Technique","Cervical Range of Motion","Neck Disability","2026-04-09",{"date":122,"type":34},"2026-04-13",{"date":124,"type":34},"2026-01-01",{"date":126,"type":21},"2026-07-15",{"name":39,"class":40},{"id":129,"slug":130,"hasResults":12,"nctId":131,"briefTitle":132,"officialTitle":132,"acronym":4,"eligibilityCriteria":133,"healthyVolunteers":77,"sex":16,"minAge":17,"maxAge":134,"enrollmentInfo":135,"targetDuration":4,"studyType":50,"phases":137,"briefSummary":138,"conditions":139,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":141,"lastUpdatePostDateStruct":142,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":41},"100627327","investigation-of-pain-perception-according-to-gender-in-individuals-with-scoliosis-100627327","NCT07447193","Investigation of Pain Perception According to Gender in Individuals With Scoliosis","Inclusion Criteria:\n\n* Having a clinical or radiological diagnosis of scoliosis\n* Being between 18-45 years of age\n* Not having undergone scoliosis surgery in the last 6 months\n* Agreeing to participate in the study voluntarily\n\nExclusion Criteria:\n\n* Having a history of neurological disease\n* Acute inflammatory spinal disease\n* Serious cardiovascular or systemic diseases that would prevent participation in exercise","45 Years",{"count":136,"type":21},50,[52],"The aim of this study is to evaluate whether pain perception under spinal pressure created on a physiotherapy roller differs according to gender in individuals diagnosed with scoliosis.",[140],"Scoliosis","2026-04-03",{"date":120,"type":34},{"date":144,"type":34},"2026-04-01",{"date":146,"type":21},"2026-06-30",{"name":39,"class":40},{"id":149,"slug":150,"hasResults":12,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":154,"eligibilityCriteria":155,"healthyVolunteers":77,"sex":156,"minAge":17,"maxAge":78,"enrollmentInfo":157,"targetDuration":4,"studyType":50,"phases":159,"briefSummary":160,"conditions":161,"keywords":163,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":168,"lastUpdatePostDateStruct":169,"startDateStruct":171,"completionDateStruct":173,"leadSponsor":175,"locationsCount":4},"100631239","the-effect-of-haptonomy-practice-on-pregnant-women-with-a-history-of-abortion-100631239","NCT07498088","THE EFFECT OF HAPTONOMY PRACTICE ON PREGNANT WOMEN WITH A HISTORY OF ABORTION.","THE EFFECT OF HAPTOTHERAPY APPLİCATİON ON PRE-NATAL ATTACHMENT AND ANXİETY LEVELS İN PREG-NANT WOMEN WİTH A HİSTORY OF ABORTİON","Haptonomy","Inclusion Criteria:\n\n* Primiparous pregnant women with a history of abortion\n* Singleton pregnant women with a healthy pregnancy between 28 and 32 weeks\n* Women who conceived naturally\n* Pregnant women without psychiatric disorders\n* Pregnant women without a diagnosed genetic disease\n* Pregnant women without a history of two or more abortions\n\nExclusion Criteria:\n\n* Pregnant women diagnosed with high-risk pregnancies during the study\n* Pregnant women who were included in the study but could not be reached\n* Pregnant women who did not continue with the treatment during the study","FEMALE",{"count":158,"type":21},80,[52],"Pregnancy is a period of comprehensive adaptation for a woman in physiological, psychological, and social terms. During this process, physical and mental transformations occur due to hormonal changes; multifaceted changes emerge, such as adopting the role of motherhood, developing a new sense of identity, and adapting to increased responsibilities. These changes during pregnancy affect not only the mother but also the fetus. Especially from the 26th week of pregnancy onwards, with the development of the fetus's auditory and sensory perception capacity, a process of reciprocal interaction begins between mother and fetus. This early interaction forms the basis of prenatal bonding.Prenatal bonding is a dynamic process involving behaviors such as the mother developing emotional closeness towards the fetus, talking to it, making contact, and preparing for care. This bonding directly affects the post-natal mother-baby relationship. However, prenatal bonding is influenced by many factors such as anxiety, stress, history of psychiatric illness, pregnancy complications, socioeconomic status, social support, and previous pregnancy experiences. Women who have experienced prenatal loss (abortion, stillbirth, neonatal death) frequently experience increased anxiety, stress, and difficulty bonding in subsequent pregnancies. High levels of uncertainty, fear, and anxiety in these individuals can negatively impact both the pregnancy and postpartum periods. The literature indicates that women who have experienced prenatal loss have lower levels of prenatal bonding and increased risks of anxiety and depression compared to those who have had healthy pregnancies. Increased stress and anxiety during the prenatal period have also been shown to be associated with negative outcomes such as low birth weight, premature birth, and neurodevelopmental problems. Therefore, supporting psychological well-being during pregnancy is critically important.In this context, interventions aimed at strengthening the bond between mother and fetus are gaining importance. Haptonomy, as a touch-based approach, is a holistic method that supports the establishment of emotional bonds between mother, father, and fetus. This method aims to develop trust-based communication by prioritizing the physical and emotional acceptance of the individual's presence. In haptonomy practices, the goal is for expectant mothers to first increase their own bodily and emotional awareness, and then to establish a conscious interaction with the fetus. Studies show that haptonomy reduces stress, anxiety, and fear of childbirth in pregnant women, while increasing prenatal bonding levels. It is also reported to have positive effects on newborns, improving their adaptation to environmental stimuli. However, the number of studies on haptonomy is limited, and research is needed, particularly focusing on its effects in pregnant women who have experienced prenatal loss. The aim of this research is to examine the effect of haptonomy on prenatal bonding and anxiety levels in pregnant women who have experienced abortion. It is hypothesized that haptonomy may strengthen mother-fetus bonding by reducing negative emotions experienced during pregnancy after a loss. The findings are expected to contribute to evidence-based care approaches applicable to high-risk pregnancy groups.",[162],"Pregnant Women",[164,165,166,167],"haptonomy","abortion","anxiety","attachment","2026-03-23",{"date":170,"type":34},"2026-03-27",{"date":172,"type":21},"2026-03-30",{"date":174,"type":21},"2026-08-28",{"name":39,"class":40},{"id":177,"slug":178,"hasResults":12,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":4,"eligibilityCriteria":182,"healthyVolunteers":77,"sex":156,"minAge":17,"maxAge":183,"enrollmentInfo":184,"targetDuration":4,"studyType":50,"phases":185,"briefSummary":186,"conditions":187,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":41},"100627425","investigation-of-the-effectiveness-of-progressive-resistance-exercise-training-in-the-management-of-lymphedema-100627425","NCT07448467","Investigation of the Effectiveness of Progressive Resistance Exercise Training in the Management of Lymphedema.","Investigating the Effectiveness of Progressive Resistance Exercise Training in the Management of Lymphedema Developing After Breast Cancer Treatment: a Randomized Controlled Trial","Inclusion criteria:\n\n* Being between 18 and 60 years of age.\n* Being included in the study 3 months after undergoing surgery.\n* Being able to tolerate compression bandages or compression garments.\n\nExclusion criteria:\n\n\\- Individuals who need to restart active cancer treatment during the study period. - Being within the first 3 months after surgery.","60 Years",{"count":136,"type":21},[52],"This study aims to investigate the effect of progressive resistance exercise training on the clinical findings and functional outcomes of lymphedema in individuals who develop upper extremity lymphedema after breast cancer treatment (surgery, chemotherapy and\u002For radiotherapy).",[188,189],"Lymphedema","Breast Cancer","2026-03-10",{"date":192,"type":34},"2026-03-12",{"date":194,"type":34},"2026-03-06",{"date":196,"type":21},"2026-08-30",{"name":39,"class":40},{"id":199,"slug":200,"hasResults":12,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":4,"eligibilityCriteria":204,"healthyVolunteers":77,"sex":16,"minAge":205,"maxAge":206,"enrollmentInfo":207,"targetDuration":4,"studyType":50,"phases":208,"briefSummary":209,"conditions":210,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":212,"startDateStruct":213,"completionDateStruct":214,"leadSponsor":216,"locationsCount":41},"100627326","the-effectiveness-of-exercise-combined-with-ergonomics-training-for-musculoskeletal-pain-seen-in-pastry-chefs-100627326","NCT07447180","The Effectiveness of Exercise Combined With Ergonomics Training for Musculoskeletal Pain Seen in Pastry Chefs","The Effectiveness of Exercise Combined With Ergonomics Training for Musculoskeletal Pain Seen in Pastry Chefs: A Randomized Controlled Trial.","Inclusion Criteria:\n\n* Having been a pastry chef for at least 5 years\n* Being registered with the pastry chefs' association\n* Not having undergone any surgical procedure affecting upper extremity function or having a serious orthopedic injury history within the last 6 months\n\nExclusion Criteria:\n\n* Not having a health problem that prevents exercise.","25 Years","50 Years",{"count":109,"type":21},[52],"This study examines the effectiveness of ergonomics training combined with exercise for musculoskeletal pain seen in pastry chefs.",[211],"Work-related Illness",{"date":192,"type":34},{"date":194,"type":34},{"date":215,"type":21},"2026-09-30",{"name":39,"class":40},{"id":218,"slug":219,"hasResults":12,"nctId":220,"briefTitle":221,"officialTitle":222,"acronym":4,"eligibilityCriteria":223,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":224,"targetDuration":4,"studyType":50,"phases":225,"briefSummary":226,"conditions":227,"keywords":231,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":237,"lastUpdatePostDateStruct":238,"startDateStruct":240,"completionDateStruct":242,"leadSponsor":244,"locationsCount":41},"100628142","virtual-reality-forest-sounds-and-patient-outcomes-during-chest-tube-removal-100628142","NCT07457788","Virtual Reality Forest Sounds and Patient Outcomes During Chest Tube Removal","The Effect of Nature Sounds in a Virtual Reality Forest During Chest Tube Removal on Pain, Vital Signs, Comfort, and Patient Satisfaction","Inclusion Criteria:\n\n* Able to speak and understand Turkish\n* Willing to participate in the study\n* Aged 18 years or older\n* No auditory or visual impairments\n\nExclusion Criteria:\n\n* Patients with impaired orientation to time and place\n* Patients with migraine, vertigo, or dizziness\n* Illiterate patients",{"count":109,"type":21},[52],"The aim of this study is to investigate the effects of listening to nature sounds in a virtual reality forest on pain, vital signs, comfort, and patient satisfaction during chest tube removal. This study aims to determine whether there are significant differences in pain, comfort, patient satisfaction, and vital signs between the experimental and control groups during chest tube removal. \"In this study, a VR video featuring a relaxing forest environment with nature sounds will be used with a virtual reality headset. Patients will be exposed to both auditory and visual stimuli. It is anticipated that the findings of this randomized controlled experimental study will make a significant contribution to the literature and clinical",[228,229,230],"Chest Tube","Virtual Reality","Chest Tube Removal",[232,233,234,235,236],"pain","chest tube","patient satisfaction","comfort","vital signs","2026-03-03",{"date":239,"type":34},"2026-03-09",{"date":241,"type":34},"2025-12-01",{"date":243,"type":21},"2026-06",{"name":39,"class":40},{"id":246,"slug":247,"hasResults":12,"nctId":248,"briefTitle":249,"officialTitle":250,"acronym":4,"eligibilityCriteria":251,"healthyVolunteers":77,"sex":252,"minAge":205,"maxAge":134,"enrollmentInfo":253,"targetDuration":4,"studyType":50,"phases":254,"briefSummary":255,"conditions":256,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":259,"lastUpdatePostDateStruct":260,"startDateStruct":261,"completionDateStruct":263,"leadSponsor":265,"locationsCount":41},"100626958","the-effectiveness-of-exercise-in-the-treatment-of-erectile-dysfunction-and-premature-ejaculation-100626958","NCT07442396","The Effectiveness of Exercise in the Treatment of Erectile Dysfunction and Premature Ejaculation","The Effectiveness of Exercise in the Treatment of Erectile Dysfunction and Premature Ejaculation: a Randomized Controlled Trial.","Inclusion Criteria\n\n* Male individuals aged 25-45 years\n* Individuals diagnosed with erectile dysfunction and premature ejaculation\n* Individuals who voluntarily agree to participate in the study and sign the informed consent form\n* Individuals who have the physical and cognitive capacity to participate in pelvic floor physiotherapy applications\n\nExclusion Criteria\n\n* Individuals with a history of surgery in the pelvic region\n* Individuals with a diagnosis of neurological disease or neurological disorder that may affect pelvic floor muscle function\n* Presence of active infection, inflammation, or painful pathology in the pelvic region\n* Individuals who regularly use medications that significantly affect sexual function\n* Individuals with serious psychiatric illness or cognitive impairment that may hinder study compliance","MALE",{"count":136,"type":21},[52],"The aim is to investigate the effectiveness of exercise in the treatment of erectile dysfunction and premature ejaculation.",[257,258],"Erectile Dysfunction","Premature Ejaculation","2026-03-02",{"date":237,"type":34},{"date":262,"type":34},"2026-03-01",{"date":264,"type":21},"2026-07-10",{"name":39,"class":40},{"id":267,"slug":268,"hasResults":12,"nctId":269,"briefTitle":270,"officialTitle":271,"acronym":4,"eligibilityCriteria":272,"healthyVolunteers":77,"sex":16,"minAge":273,"maxAge":183,"enrollmentInfo":274,"targetDuration":4,"studyType":50,"phases":275,"briefSummary":276,"conditions":277,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":259,"lastUpdatePostDateStruct":279,"startDateStruct":280,"completionDateStruct":281,"leadSponsor":282,"locationsCount":41},"100626957","the-effect-of-exercise-and-ergonomics-training-program-on-musculoskeletal-disorders-in-teachers-100626957","NCT07442383","The Effect of Exercise and Ergonomics Training Program on Musculoskeletal Disorders in Teachers","The Effect of Exercise and Ergonomics Training Program on Musculoskeletal Disorders in Teachers: A Randomized Controlled Trial","Inclusion Criteria\n\n* Being between 30-60 years old\n* Having been a teacher for at least 5 years\n* Having experienced musculoskeletal pain for at least three months\n* Being able to participate in the ergonomics training and exercise program planned during the study period\n\nExclusion Criteria\n\n* Having a pain score below 3 on the Visual Analog scale\n* Having a neurological or orthopedic disease that prevents exercise\n* Having undergone musculoskeletal surgery within the last six months\n* Having a psychological disorder that may prevent exercise","30 Years",{"count":158,"type":21},[52],"Comparing the effectiveness of ergonomics and exercise training given to teachers regarding musculoskeletal disorders.",[278],"Work-related Injury",{"date":237,"type":34},{"date":262,"type":34},{"date":196,"type":21},{"name":39,"class":40},{"id":284,"slug":285,"hasResults":12,"nctId":286,"briefTitle":287,"officialTitle":288,"acronym":4,"eligibilityCriteria":289,"healthyVolunteers":77,"sex":16,"minAge":206,"maxAge":290,"enrollmentInfo":291,"targetDuration":4,"studyType":50,"phases":292,"briefSummary":293,"conditions":294,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":259,"lastUpdatePostDateStruct":297,"startDateStruct":298,"completionDateStruct":299,"leadSponsor":301,"locationsCount":41},"100626956","the-effect-of-functional-rotational-exercises-on-fall-risk-and-mobility-in-parkinsons-disease-patients-100626956","NCT07442370","The Effect of Functional Rotational Exercises on Fall Risk and Mobility in Parkinson's Disease Patients","The Effect of Functional Rotational Exercises on Fall Risk and Mobility in Parkinson's Disease Patients: A Randomized Controlled Study","Inclusion Criteria\n\n* Individuals with a clinical diagnosis of idiopathic Parkinson's disease (Hoehn \\& Yahr stages 1-2)\n* Individuals aged 50-70 years\n* Mini Mental State Test score ≥ 24\n* Individuals whose medical treatment has been stable in the last 6 weeks\n* Individuals with stable vital signs\n* Individuals who volunteer to participate in the study and understand the purpose and process of the study, and who have signed a written informed consent form\n\nExclusion Criteria\n\n* Advanced Parkinson's disease (H\\&Y 3-5)\n* Severe orthopedic problems\n* Vestibular system disorders\n* History of serious falls in the last 6 months","70 Years",{"count":136,"type":21},[52],"This study aims to contribute to clinical applications by investigating the effectiveness of functional rotation exercises on fall risk, mobility, and balance in patients diagnosed with idiopathic Parkinson's disease.",[295,296],"Parkinson Disease","Parkinsonism",{"date":237,"type":34},{"date":262,"type":34},{"date":300,"type":21},"2026-09-15",{"name":39,"class":40},{"id":303,"slug":304,"hasResults":12,"nctId":305,"briefTitle":306,"officialTitle":307,"acronym":4,"eligibilityCriteria":308,"healthyVolunteers":77,"sex":156,"minAge":205,"maxAge":206,"enrollmentInfo":309,"targetDuration":4,"studyType":50,"phases":310,"briefSummary":311,"conditions":312,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":259,"lastUpdatePostDateStruct":313,"startDateStruct":314,"completionDateStruct":315,"leadSponsor":316,"locationsCount":41},"100626959","the-effect-of-ergonomics-and-exercise-training-on-musculoskeletal-disorders-in-female-dairy-farmers-100626959","NCT07442409","The Effect of Ergonomics and Exercise Training on Musculoskeletal Disorders in Female Dairy Farmers","The Effect of Ergonomics and Exercise Training on Musculoskeletal Disorders in Female Dairy Farmers: A Randomized Controlled Trial","Inclusion Criteria\n\n* Having been actively engaged in farming for at least 5 years\n* Being between 25-50 years of age\n* Being female\n* Having the physical ability to participate in the planned training and exercise program during the study period\n\nExclusion Criteria\n\n* Having any accompanying neurological disease or neurological dysfunction\n* Having a history of any musculoskeletal surgery\n* Having a serious systemic disease that may prevent the implementation of the study protocol",{"count":109,"type":21},[52],"The aim of this research is to comparatively examine the effects of ergonomics training and the combined application of ergonomics and structured exercise training on work-related musculoskeletal disorders in female farmers actively engaged in milking.",[278,211],{"date":237,"type":34},{"date":262,"type":34},{"date":196,"type":21},{"name":39,"class":40},{"id":318,"slug":319,"hasResults":12,"nctId":320,"briefTitle":321,"officialTitle":322,"acronym":323,"eligibilityCriteria":324,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":325,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":327,"conditions":328,"keywords":331,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":337,"lastUpdatePostDateStruct":338,"startDateStruct":340,"completionDateStruct":341,"leadSponsor":343,"locationsCount":41},"100620322","association-of-high-paindetect-scores-with-pain-region-and-diagnosis-in-patients-attending-a-musculoskeletal-and-sports-medicine-clinic-100620322","NCT07356115","Association of High PainDETECT Scores With Pain Region and Diagnosis in Patients Attending a Musculoskeletal and Sports Medicine Clinic","Evaluation of the Association Between PainDETECT Scores, Pain Localization, and Diagnosis in a Musculoskeletal and Sports Medicine Outpatient Population","PD-MSK","Inclusion Criteria:\n\n* Patients aged 18 years and older\n* Patients who presented to the musculoskeletal and sports medicine clinic with pain complaints\n* Availability of complete medical records including PainDETECT questionnaire data\n\nExclusion Criteria:\n\n* Patients younger than 18 years\n* Incomplete clinical or questionnaire data",{"count":326,"type":21},150,"This observational study aims to evaluate the relationship between PainDETECT questionnaire scores, pain regions, and clinical diagnoses in patients presenting to a musculoskeletal and sports medicine clinic. Patients attending the clinic will complete the PainDETECT questionnaire, and their pain localization and clinical diagnoses will be recorded. The findings are expected to contribute to a better understanding of neuropathic pain components in musculoskeletal conditions.",[329,330],"Musculoskeletal Pain","Neuropathic Pain",[332,333,334,335,336,330],"PainDETECT","Retrospective Study","Patient-Reported Outcome","Pain Assessment","Chronic Pain","2026-02-19",{"date":339,"type":34},"2026-02-23",{"date":337,"type":34},{"date":342,"type":21},"2026-03-20",{"name":39,"class":40},{"id":345,"slug":346,"hasResults":12,"nctId":347,"briefTitle":348,"officialTitle":349,"acronym":350,"eligibilityCriteria":351,"healthyVolunteers":77,"sex":16,"minAge":17,"maxAge":107,"enrollmentInfo":352,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":354,"conditions":355,"keywords":358,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":363,"lastUpdatePostDateStruct":364,"startDateStruct":365,"completionDateStruct":367,"leadSponsor":369,"locationsCount":41},"100625386","investigation-of-the-relationship-between-periodontitis-and-sleep-quality-100625386","NCT07421960","Investigation of the Relationship Between Periodontitis and Sleep Quality","An Evaluation of the Relationship Between Sleep Quality and Periodontitis","RBPSQ","Inclusion Criteria:\n\n* systemically healthy,\n* clinical diagnosis of periodontitis,\n* clinical diagnosis of periodontal health\n\nExclusion Criteria:\n\n* history of regular use of systemic antibiotics, anti-inflammatory, or antioxidant drugs (previous 6 months);\n* nonsurgical periodontal treatment (previous 6 months);\n* surgical periodontal treatment (previous 12 months);\n* presence of \\\u003C20 teeth;\n* current medications affecting gingival health (calcium channel blockers, phenytoin, cyclosporine, and hormone replacement therapy);\n* diabetes diagnosis; rheumatoid arthritis diagnosis; and pregnancy, lactating, or excessive alcohol consumption.",{"count":353,"type":21},48,"This project aims to investigate the relationship between periodontitis and sleep quality. Its originality lies in evaluating the association between periodontal status and sleep quality together with salivary interleukin-6 (IL-6), interleukin-6 (IL-10) IL-10, and pentraxin-3 levels. In particular, examining the relationship of sleep quality with biological, psychological, and lifestyle factors through periodontitis and salivary IL-6, IL-10, and pentraxin-3 levels has not been previously studied in the literature. Methodologically, periodontal status will be determined through clinical examination; participants' Pittsburgh Sleep Quality Index and Multidimensional Fatigue Inventory scores will be recorded; and salivary IL-6, IL-10, and pentraxin-3 levels will be measured. The obtained data will be compared using statistical analyses to determine the strength of the relationship between periodontitis severity and sleep quality. From a management perspective, the project will be conducted following approval from the ethics committee. In terms of broader impact, the results are expected to scientifically demonstrate the relationship between periodontitis and sleep quality, contribute to the adoption of a holistic health approach in clinical practice, and increase public health awareness. Additionally, the project is expected to provide a foundation for future research on the relationship between oral health and quality of life.",[356,357,83,27],"Periodontitis","Periodontal Disease",[359,360,361,362,86],"IL-6","IL-10","pentraxin","periodontitis","2026-02-12",{"date":337,"type":34},{"date":366,"type":34},"2026-02-10",{"date":368,"type":21},"2026-05-08",{"name":39,"class":40},{"id":371,"slug":372,"hasResults":12,"nctId":373,"briefTitle":374,"officialTitle":375,"acronym":4,"eligibilityCriteria":351,"healthyVolunteers":77,"sex":16,"minAge":17,"maxAge":107,"enrollmentInfo":376,"targetDuration":378,"studyType":22,"phases":4,"briefSummary":379,"conditions":380,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":384,"lastUpdatePostDateStruct":385,"startDateStruct":387,"completionDateStruct":389,"leadSponsor":391,"locationsCount":41},"100616971","association-of-periodontal-status-and-smoking-with-salivary-inflammasome-markers-100616971","NCT07312552","Association of Periodontal Status and Smoking With Salivary Inflammasome Markers","The Impact of Periodontal Status and Smoking on Salivary Inflammasome Levels: A Cross-Sectional Study",{"count":377,"type":21},116,"1 Day","The aim of this study is to evaluate the relationship between periodontal status and salivary levels of the inflammasomes NOD-like receptor family, pyrin domain containing 3 (NLRP-3), NOD-like receptor family, pyrin domain containing 6 (NLRP-6), NOD-like receptor family, pyrin domain containing 12 (NLRP-12), NOD-like receptor family, CARD domain containing 5 (NLRC-5), interleukin-1 beta (IL-1β) and interleukin-10 (IL-10). Furthermore, this study aims to investigate whether the salivary levels of these inflammasomes may serve as potential diagnostic biomarkers for distinguishing individuals with periodontitis from those without. In addition, the potential role of smoking in modulating the relationship between periodontal status and salivary inflammasome levels will also be explored.",[356,357,381,382,383],"Periodontal Health","Smoking","Inflammasomes","2026-01-17",{"date":386,"type":34},"2026-01-21",{"date":388,"type":34},"2025-12-23",{"date":390,"type":21},"2026-07",{"name":39,"class":40},{"id":393,"slug":394,"hasResults":12,"nctId":395,"briefTitle":396,"officialTitle":397,"acronym":4,"eligibilityCriteria":398,"healthyVolunteers":77,"sex":16,"minAge":399,"maxAge":400,"enrollmentInfo":401,"targetDuration":4,"studyType":50,"phases":402,"briefSummary":403,"conditions":404,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":407,"lastUpdatePostDateStruct":408,"startDateStruct":410,"completionDateStruct":411,"leadSponsor":413,"locationsCount":41},"100618551","investigation-of-the-effects-of-proprioceptive-exercises-after-anterior-cruciate-ligament-surgery-100618551","NCT07333092","Investigation of the Effects of Proprioceptive Exercises After Anterior Cruciate Ligament Surgery","Investigation of the Effects of Proprioceptive Exercises on Balance, Kinesiophobia, and Functionality After Anterior Cruciate Ligament Surgery: A Randomized Controlled Trial","Inclusion Criteria\n\n* Being between 20-40 years of age\n* Having undergone anterior cruciate ligament (ACL) surgery\n* Being in the 2nd week of rehabilitation after ACL surgery\n\nExclusion Criteria\n\n* Having a concomitant meniscus injury\n* Having a concomitant medial collateral ligament injury\n* Being in the 1st week of rehabilitation after ACL surgery","20 Years","40 Years",{"count":136,"type":21},[52],"The aim of this study is to investigate the effects of proprioceptive exercises on balance, kinesiophobia, and functionality after anterior cruciate ligament surgery.",[405,406],"Anterior Cruciate Ligament Injuries","Anterior Cruciate Ligament Rupture","2026-01-15",{"date":409,"type":34},"2026-01-20",{"date":407,"type":34},{"date":412,"type":21},"2026-08-20",{"name":39,"class":40},{"id":415,"slug":416,"hasResults":12,"nctId":417,"briefTitle":418,"officialTitle":418,"acronym":4,"eligibilityCriteria":419,"healthyVolunteers":77,"sex":252,"minAge":17,"maxAge":107,"enrollmentInfo":420,"targetDuration":4,"studyType":50,"phases":421,"briefSummary":422,"conditions":423,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":407,"lastUpdatePostDateStruct":425,"startDateStruct":427,"completionDateStruct":429,"leadSponsor":430,"locationsCount":41},"100617336","extracorporeal-shockwave-therapy-in-the-treatment-of-peyronies-disease-100617336","NCT07317297","Extracorporeal Shockwave Therapy in the Treatment of Peyronie's Disease","Inclusion Criteria:\n\n* Male individuals aged 18-65 years.\n* Having been diagnosed with Peyronie's Disease that has been stable (without increasing pain and curvature) for at least 6 months.\n* Presence of palpable penile plaque.\n\nExclusion Criteria:\n\n* Acute inflammatory stage (painful, progressive)\n* Having previously undergone surgery, needle therapy (e.g., Xiaflex), or Extracorporeal Shockwave Therapy for peyronie's disease.\n* Uncontrolled diabetes, severe coagulopathy, or receiving anticoagulant therapy.\n* History of penile cancer.\n* Severe erectile dysfunction.\n* Patients who are considered unable to comply with the study protocol or who cannot attend follow-up visits.",{"count":136,"type":21},[52],"Investigation of the effectiveness of extracorporeal shock wave therapy in the treatment of Peyronie's disease.",[424],"Peyronie Disease",{"date":426,"type":34},"2026-01-16",{"date":428,"type":34},"2026-01-10",{"date":172,"type":21},{"name":39,"class":40},{"id":432,"slug":433,"hasResults":12,"nctId":434,"briefTitle":435,"officialTitle":436,"acronym":437,"eligibilityCriteria":438,"healthyVolunteers":12,"sex":16,"minAge":439,"maxAge":4,"enrollmentInfo":440,"targetDuration":4,"studyType":50,"phases":441,"briefSummary":442,"conditions":443,"keywords":445,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":453,"lastUpdatePostDateStruct":454,"startDateStruct":456,"completionDateStruct":458,"leadSponsor":460,"locationsCount":461},"100615048","effects-of-photobiomodularion-on-brain-connectivity-and-cognitive-function-in-cognitive-impairment-100615048","NCT07287527","Effects of Photobiomodularion on Brain Connectivity and Cognitive Function in Cognitive Impairment","The Effects of Transcranial Photobiomodulation (t-PBM) on Cognitive Performance and Functional Brain Connectivity in Patients With Mild Cognitive Impairment and the Role of Genetic Factors","PBM-CogConnect","Inclusion Criteria:\n\n* Age 55 years or older\n* Diagnosis of amnestic Mild Cognitive Impairment (aMCI)\n\nExclusion Criteria:\n\n* Presence of a neurological disorder\n* Presence of a severe psychiatric disorder\n* Having a pacemaker or other implanted medical device that is not MRI-compatible","55 Years",{"count":109,"type":21},[52],"The goal of this clinical trial is to learn if transcranial photobiomodulation (t-PBM), a light-based brain therapy, can help improve memory and cognitive skills in older adults with amnestic mild cognitive impairment (aMCI). This condition involves memory problems that are greater than normal aging and may increase the chance of developing Alzheimer's disease.\n\nThe main questions this study aims to answer are:\n\n1. Does t-PBM, when used together with cognitive training, improve memory and cognitive skills?\n2. Does t-PBM change how certain brain areas communicate with each other, especially in the default mode network (DMN)?\n\nResearchers will compare:\n\nt-PBM plus cognitive training to sham (inactive) t-PBM plus the same cognitive training to see if the active light treatment leads to better cognitive improvement and healthier brain activity.\n\nParticipants will:\n\n* Provide a blood sample so the research team can create a genetic profile;\n* Complete cognitive tests before and after the 4-week program;\n* Meet with a dietitian before and after the program so the research team can make sure diet stays consistent and does not influence brain results;\n* Have a brain fMRI scan before and after treatment to measure brain connectivity changes;\n* Take part in eight sessions of cognitive training;\n* Receive either active t-PBM or sham t-PBM during these sessions.",[444],"AMCI - Amnestic Mild Cognitive Impairment",[446,447,448,449,450,451,452],"t-PBM","aMCI","fMRI","Cognitive Rehabilitation","functional connectivity","APOE","COMT","2025-12-13",{"date":455,"type":34},"2025-12-17",{"date":457,"type":34},"2024-03-30",{"date":459,"type":21},"2026-10",{"name":39,"class":40},2,{"id":463,"slug":464,"hasResults":12,"nctId":465,"briefTitle":466,"officialTitle":467,"acronym":4,"eligibilityCriteria":468,"healthyVolunteers":12,"sex":16,"minAge":17,"maxAge":469,"enrollmentInfo":470,"targetDuration":4,"studyType":50,"phases":471,"briefSummary":472,"conditions":473,"keywords":477,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":481,"lastUpdatePostDateStruct":482,"startDateStruct":484,"completionDateStruct":485,"leadSponsor":486,"locationsCount":4},"100609280","benson-relaxation-exercises-and-sleep-quality-in-lung-cancer-patients-100609280","NCT07212517","Benson Relaxation Exercises and Sleep Quality in Lung Cancer Patients","The Effect of Benson Relaxation Exercises on Sleep Quality in Patients With Lung Cancer","Inclusion Criteria:\n\n* Patients aged 18 years and over,\n* Have been diagnosed with lung cancer and be receiving inpatient treatment,\n* Be conscious and able to communicate,\n* Agree to participate in breathing exercises during the study,\n* Score above 5 on the PSQI,\n* Sign a written informed consent form.\n\nExclusion Criteria:\n\n* Patients under 18 years of age,\n* Those with additional mental or cognitive disorders,\n* Those with physiological barriers to performing breathing exercises,\n* Those unable to complete the programme during the study period,\n* Those with a PSQI score above 5,\n* Those who violated the study protocol,\n\n  •. Those with an oxygen saturation value below 90,\n* Those scoring above 5 on the Visual Pain Scale,\n* Those who have previously practised yoga or meditation,\n* Patients with haemoptysis,\n* Patients taking any anxiolytic or hypnotic medication.\n\n  * During the 15 days of Benson relaxation exercise, patients in both the intervention and control groups will not be allowed to perform the exercise if their O2 saturation and pain level changes meet the exclusion criteria.","80 Years",{"count":109,"type":21},[52],"The aim of this study is to investigate the effect of Benson Relaxation Exercises on sleep quality in hospitalized patients diagnosed with lung cancer. It is planned to be conducted as a randomized controlled trial.\n\nHypotheses of the Study H1: The sleep quality of lung cancer patients who undergo Benson relaxation exercises is statistically significantly better than that of patients who do not undergo such exercises.\n\nH2: There is no significant difference in sleep quality between patients who undergo Benson relaxation exercises and those who do not.",[83,474,475,476],"Relaxation","Canser","Benson Exercise",[478,479,480],"cancer patient","Benson relaxation","sleep Quality","2025-09-30",{"date":483,"type":34},"2025-10-08",{"date":481,"type":21},{"date":126,"type":21},{"name":39,"class":40},{"id":488,"slug":489,"hasResults":12,"nctId":490,"briefTitle":491,"officialTitle":492,"acronym":4,"eligibilityCriteria":493,"healthyVolunteers":12,"sex":16,"minAge":494,"maxAge":399,"enrollmentInfo":495,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":497,"conditions":498,"keywords":500,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":517,"lastUpdatePostDateStruct":518,"startDateStruct":520,"completionDateStruct":522,"leadSponsor":524,"locationsCount":41},"100607339","assessment-of-respiratory-parameters-aerobic-capacity-and-sleep-quality-in-thoracic-ais-100607339","NCT07187271","Assessment of Respiratory Parameters, Aerobic Capacity and Sleep Quality in Thoracic AIS","Comparison of Respiratory Parameters, Aerobic Capacity, and Sleep Quality in Individuals With Thoracic Adolescent Idiopathic Scoliosis","Inclusion Criteria:\n\nIndividuals with a Cobb angle greater than 10 degrees Adolescents aged 12-20 years diagnosed with thoracic Adolescent Idiopathic Scoliosis, classified as T-type or TL-type according to ISST classification Patients currently undergoing brace treatment\n\nExclusion Criteria:\n\nIndividuals with a history of spinal surgery Individuals with neurological disorders Individuals with a diagnosed psychiatric disorder Pregnant individuals Individuals who do not provide consent to participate in the study","12 Years",{"count":496,"type":21},30,"This study aims to compare respiratory parameters -including pulmonary function and respiratory muscle strength-as well as aerobic capacity and sleep quality in individuals with thoracic adolescent idiopathic scoliosis. Participants will be categorized according to the ISST classification into T-type and TL-type curvature patterns. The study will evaluate differences between these groups using standardized clinical assessments.",[499],"Adolescent Idiopathic Scoliosis",[501,502,503,504,505,506,507,508,509,510,511,512,513,514,515,516],"AIS","ISST classification","Thoracic AIS","Thoracolumbar AIS","Cobb angle","Angle of Trunk Rotation (ATR)","Pulmonary function test","FEV1","FVC","Respiratory muscle strength","MIP (Maximal Inspiratory Pressure)","MEP (Maximal Expiratory Pressure)","Aerobic capacity","Incremental Shuttle Walk Test (ISWT)","PUKİ (Pittsburgh Sleep Quality Index)","SAQ (Scoliosis Appearance Questionnaire)","2025-09-19",{"date":519,"type":34},"2025-09-22",{"date":521,"type":21},"2025-10-05",{"date":523,"type":21},"2025-12-15",{"name":39,"class":40},{"id":526,"slug":527,"hasResults":12,"nctId":528,"briefTitle":529,"officialTitle":530,"acronym":531,"eligibilityCriteria":532,"healthyVolunteers":77,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":533,"targetDuration":4,"studyType":50,"phases":534,"briefSummary":535,"conditions":536,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":538,"lastUpdatePostDateStruct":539,"startDateStruct":541,"completionDateStruct":543,"leadSponsor":545,"locationsCount":461},"100599667","simulation-psychosocial-care-skills-and-oncology-nursing-100599667","NCT07087470","Simulation Psychosocial Care Skills and Oncology Nursing","The Effect of Simulation Based Psychosocial Care Skill Development Programme on Psychosocial Care Competencies and Professional Life Quality of Oncology Nurses","SPCSAON","Inclusion Criteria:\n\n* 6 months or more experience of working with oncology patients\n* Not having received training on psychosocial care skills after graduation\n* Oncology nurses who volunteered to participate in the study\n\nExclusion Criteria:\n\n* Having less than 6 months of experience working with oncology patients\n* To have received training on psychosocial care skills after graduation\n* Not volunteering to participate in the research",{"count":109,"type":21},[52],"The aim of this study was to reveal the effect of simulation-based experience-based psychosocial care skills development programme on psychosocial care skills competence and professional quality of life of nurses working with oncology patients.\n\nThe hypotheses of the study will be tested in accordance with the following guidelines.\n\nHypothesis 1 The post-training psychosocial care competency levels of the nurses who underwent simulation-based psychosocial care skills development programme (SDPBSP) are higher than the group who underwent standard psychosocial care skills training (SPBBE).\n\nHypothesis 2 The post-training compassion fatigue levels of the nurses who underwent the SDPBI development programme were lower than the SPBBE group.\n\nHypothesis 3 The post-training burnout score levels of the nurses who underwent SPBBE development programme were lower than the group who underwent standard SPBBE.\n\nHypothesis 4 The post-training compassion satisfaction levels of the nurses who underwent SPBBE development programme are higher than the group who underwent standard SPBBE.\n\nHypothesis 5\n\nThe psychosocial care competency levels of the nurses who underwent SPBBE development programme at the 1-month post-training follow-up were higher than those who did not receive SPBBE training.\n\nHypothesis 6 At the 1-month follow-up after the training, the compassion fatigue levels of the nurses who underwent SPBBE development programme were lower than the group who underwent SPBBE and did not receive training.\n\nHypothesis 7 In the 1-month follow-up after the training, the mean burnout scores of the nurses who underwent SPBBE development programme were lower than those of the group who underwent SPBBE and did not receive training.\n\nHypothesis 8 In the 1-month follow-up after the training, the mean compassion satisfaction scores of the nurses who underwent the SPBBE development programme were higher than the SPBBE training and non-training groups.\n\nHypothesis 9 After the SDPBE programme, the psychosocial skills training scores of those who received SDPBE are higher than those who did not receive training.\n\nHypothesis 10 At the 1-month follow-up after the SDPBE programme, the psychosocial skills training scores of those who received SDPBE were higher than those who did not receive training.",[537],"Simulation-based Training","2025-07-18",{"date":540,"type":34},"2025-07-28",{"date":542,"type":34},"2025-03-15",{"date":544,"type":21},"2025-11-30",{"name":39,"class":40},{"id":547,"slug":548,"hasResults":12,"nctId":549,"briefTitle":550,"officialTitle":551,"acronym":4,"eligibilityCriteria":552,"healthyVolunteers":77,"sex":16,"minAge":273,"maxAge":183,"enrollmentInfo":553,"targetDuration":4,"studyType":50,"phases":554,"briefSummary":555,"conditions":556,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":559,"lastUpdatePostDateStruct":560,"startDateStruct":562,"completionDateStruct":563,"leadSponsor":564,"locationsCount":41},"100570590","robotic-rehabilitation-and-dual-task-exercises-in-hemiplegic-patients-100570590","NCT06709222","Robotic Rehabilitation and Dual-Task Exercises in Hemiplegic Patients","Investigation of the Effectiveness of Dual-Task Exercises Applied in Addition to Robotic Rehabilitation in Hemiplegic Patients: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Diagnosis of post-stroke hemiplegia (hemiplegia onset must be between 3 months and 1 year).\n* Age range: 30-60 years.\n* Voluntariness to participate in rehabilitation.\n* Patients with a motor function loss of 30-70% according to Fugl-Meyer Motor Assessment results.\n* Literacy\n\nExclusion Criteria:\n\n* History of active psychiatric disease.\n* Severe joint deformities or other neurological diseases.\n* Having had a recent stroke during rehabilitation.",{"count":20,"type":21},[52],"The aim of this study was to investigate the effectiveness of dual-task exercises combined with robotic rehabilitation applied to post-stroke hemiplegia patients.",[557,558],"Cognitive Coping","Hemiplegia","2025-07-16",{"date":561,"type":34},"2025-07-20",{"date":453,"type":21},{"date":172,"type":21},{"name":39,"class":40},{"id":566,"slug":567,"hasResults":12,"nctId":568,"briefTitle":569,"officialTitle":570,"acronym":4,"eligibilityCriteria":571,"healthyVolunteers":12,"sex":16,"minAge":572,"maxAge":494,"enrollmentInfo":573,"targetDuration":4,"studyType":50,"phases":575,"briefSummary":576,"conditions":577,"keywords":580,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":585,"lastUpdatePostDateStruct":586,"startDateStruct":588,"completionDateStruct":590,"leadSponsor":592,"locationsCount":4},"100584736","the-effect-of-virtual-reality-goggles-and-distraction-cards-applied-to-children-aged-6-12-years-during-inhaler-therapy-on-physiological-parameters-and-anxiety-100584736","NCT06893237","The Effect of Virtual Reality Goggles and Distraction Cards Applied to Children Aged 6-12 Years During Inhaler Therapy on Physiological Parameters and Anxiety","The Effect of Virtual Reality Goggles and Distraction Cards Applied to Children Aged 6-12 Years During Inhaler Therapy on Physiological Parameters and Anxiety: a Randomised Controlled Study","Inclusion Criteria:\n\n* The child is receiving inhalation (salbutamol) treatment in the pediatric intensive care unit.\n* The child must be between 6-12 years old\n* The child must not have any vision or hearing problems.\n* Being conscious and being able to communicate verbally\n* After being informed, the child and parent agree to participate in the study in writing and verbally\n* No genetic, congenital, chronic or metabolic disease\n* The child has no signs of respiratory failure\n\nExclusion Criteria:\n\n* The child's clinical treatment is due to a history of surgery,\n* The child is taking a sedative medication,\n* The child has a fever over 37°C,\n* The child has applied with a severe asthma attack,\n* The child's saturation value is below 92% at the time of application.","6 Years",{"count":574,"type":21},108,[52],"In the literature, studies examining the effect of virtual reality application on physiological parameters and anxiety during inhalation therapy, which is frequently used in children, are quite limited. Therefore, this study will be conducted to determine the effect of virtual reality goggles and distraction cards on physiological parameters and anxiety in patients receiving inhalation therapy.",[578,579],"Respiratory Infections, Acute","Respiratory Tract Diseases",[581,582,583,166,584],"inhalation therapy","child","virtual reality glasses","distraction of attention","2025-03-25",{"date":587,"type":34},"2025-03-30",{"date":589,"type":21},"2025-04",{"date":591,"type":21},"2026-04",{"name":39,"class":40},{"id":594,"slug":595,"hasResults":12,"nctId":596,"briefTitle":597,"officialTitle":597,"acronym":4,"eligibilityCriteria":598,"healthyVolunteers":77,"sex":16,"minAge":205,"maxAge":134,"enrollmentInfo":599,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":601,"conditions":602,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":604,"lastUpdatePostDateStruct":605,"startDateStruct":606,"completionDateStruct":607,"leadSponsor":609,"locationsCount":41},"100580937","the-relationship-between-ergonomic-knowledge-of-healthcare-professionals-and-musculoskeletal-disorders-100580937","NCT06843798","The Relationship Between Ergonomic Knowledge of Healthcare Professionals and Musculoskeletal Disorders","Inclusion Criteria:\n\n* Being between 25 and 45 years old.\n* Being a health worker\n* Having at least 2 years of work experience\n\nExclusion Criteria:\n\n* Participant having a musculoskeletal disorder before the study\n* Having had surgery within 6 months\n* Being pregnant\n* Having a traumatic accident or injury that would affect the study",{"count":600,"type":21},400,"This study aims to investigate the relationship between the ergonomic awareness levels of Healthcare Workers and musculoskeletal disorders.",[603],"Occupational Diseases","2025-03-24",{"date":585,"type":34},{"date":542,"type":34},{"date":608,"type":21},"2025-04-01",{"name":39,"class":40},""]