[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Muş Alparslan University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":469},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,19,0,[8,45,74,103,128,157,184,213,235,253,273,293,315,338,364,387,411,425,451],{"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":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100613468","multisensory-methods-and-patient-comfort-in-thyroid-biopsy-100613468",false,"NCT07266987","Multisensory Methods and Patient Comfort in Thyroid Biopsy","The Effect ofMultisensory Methods on Pain, Anxiety, and Comfort Levels in Patients Undergoing Thyroid Biopsy","Inclusion Criteria:\n\nLiterate individuals who can read and write Aged 18 years and older Scheduled to undergo thyroid (goiter) biopsy in the interventional radiology unit Voluntarily agreeing to participate in the study and providing informed consent No diagnosed psychiatric or cognitive impairment that may affect participation\n\nExclusion Criteria:\n\nPresence of a diagnosed psychiatric disorder that may affect response reliability (e.g., bipolar disorder, dementia, schizophrenia) Previous history of thyroid biopsy Visual or hearing impairments that prevent viewing or understanding the intervention video Refusal to participate or withdrawal of consent at any stage of the study","ALL","18 Years","90 Years",{"count":20,"type":21},68,"ESTIMATED","INTERVENTIONAL",[24],"NA","This quasi-experimental study aims to determine the effect of watching an therapeutic video on patients' pain, anxiety, and comfort levels during thyroid biopsy procedures. The study will be conducted in the interventional radiology unit of Muş State Hospital between July 30, 2025, and August 28, 2026. A total of 68 patients (34 experimental and 34 control) will be included. Data will be collected using the Descriptive Information Form, Visual Analog Scale for Pain (VAS-Pain), State Anxiety Inventory, and Visual Analog Scale for Comfort (VAS-Comfort). The intervention group will watch a relaxing video immediately before and during the biopsy procedure, while the control group will receive standard care. Pre- and post-test measurements will be compared to evaluate changes in pain, anxiety, and comfort levels",[27],"Pain",[29,30,31],"pain","patient","nursing care","RECRUITING","2026-05-04",{"date":35,"type":36},"2026-05-08","ACTUAL",{"date":38,"type":36},"2025-07-20",{"date":40,"type":21},"2026-04-30",{"name":42,"class":43},"Muş Alparslan University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100632310","effects-of-postoperative-video-assisted-early-mobilization-on-recovery-outcomes-100632310","NCT07512024","Effects of Postoperative Video-assisted Early Mobilization on Recovery Outcomes","The Effect of Video-assisted Early Mobilization Training on Patient Outcomes in Individuals Undergoing Laparoscopic Cholecystectomy: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18 to 65 years.\n* Scheduled for elective laparoscopic cholecystectomy.\n* Classified as ASA I or ASA II according to the American Society of Anesthesiologists Physical Status Classification.\n* Ability to read and understand Turkish.\n* Adequate cognitive capacity to understand video education and operate the wearable activity tracker.\n* Willingness to participate and signing the informed consent form\n\nExclusion Criteria:\n\n* Chronic pain syndrome or severe chronic orthopedic\u002Frheumatologic pain conditions.\n* Pre-existing mobility limitations.\n* Endocrine or metabolic diseases affecting cortisol or glucose (e.g., diabetes, thyroid disorders, Addison's disease, Cushing's syndrome).\n* Use of medications affecting the HPA axis (e.g., systemic corticosteroids, chronic opioids, high-dose benzodiazepines).\n* Diagnosed severe psychiatric or cognitive disorders (e.g., dementia, major depression).\n* Skin allergies or medical device contraindications preventing use of the activity tracker.\n* Conversion to open surgery or major intraoperative complications.","65 Years",{"count":54,"type":21},44,[24],"This randomized controlled trial aims to evaluate the effects of video-assisted early mobilization education on postoperative recovery in patients undergoing laparoscopic cholecystectomy. As part of the intervention, structured and professionally produced educational videos will be used to explain the physiological benefits of early mobilization in the preoperative period and to demonstrate step-by-step mobilization techniques in the postoperative period.\n\nPatients in the intervention group will receive video-assisted mobilization education in addition to standard postoperative care, while patients in the control group will receive standard care alone. Physical activity levels will be objectively monitored using wearable activity tracking devices during the first 24 hours after surgery.\n\nThe study will assess the effects of video-assisted early mobilization education on postoperative physiological stress response, pain, nausea and vomiting, blood glucose levels, mobilization performance, gastrointestinal recovery, length of hospital stay, and patient satisfaction. In addition, postoperative complications, emergency department visits, and hospital readmissions within 30-days after surgery will be evaluated as exploratory outcomes.",[58],"Cholelithiasis",[60,61,62,63,64],"Postoperative Recovery","Enhanced Recovery After Surgery (ERAS)","Early Mobilization","Surgical Stress Response","Postoperative Pain","NOT_YET_RECRUITING","2026-04-04",{"date":68,"type":36},"2026-04-09",{"date":70,"type":21},"2026-05",{"date":72,"type":21},"2027-01",{"name":42,"class":43},{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":81,"sex":16,"minAge":17,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":22,"phases":85,"briefSummary":86,"conditions":87,"keywords":89,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":4},"100631977","acute-effects-of-patellar-tendon-ultrasound-on-countermovement-jump-performance-100631977","NCT07507695","Acute Effects of Patellar Tendon Ultrasound on Countermovement Jump Performance","Acute Effects of Therapeutic Ultrasound Applied to the Patellar Tendon on Countermovement Jump Performance: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Healthy university students aged 18-35 years\n* No history of lower extremity injury or surgery in the past 12 months\n* No current musculoskeletal or neurological disorders affecting the lower limbs\n\nExclusion Criteria:\n\n* History of patellar tendon injury or knee pain\n* Contraindications to therapeutic ultrasound (e.g., skin lesions, open wounds at the knee, or implanted electronic devices)\n* Any cardiovascular, neurological, or musculoskeletal condition that may affect jump performance\n* Use of medications that could affect neuromuscular function (e.g., muscle relaxants)",true,"35 Years",{"count":84,"type":21},40,[24],"This randomized, double-blind, controlled trial aims to investigate the acute effects of therapeutic ultrasound applied to the patellar tendon on vertical jump performance in healthy university students. Therapeutic ultrasound is widely used in physiotherapy to influence soft tissue properties through thermal and mechanical effects; however, its immediate impact on explosive lower-extremity performance and neuromuscular function remains unclear.\n\nParticipants will be randomly assigned to either a therapeutic ultrasound group or a sham ultrasound (placebo) group. In the intervention group, therapeutic ultrasound will be applied to the patellar tendon using a frequency of 1 MHz and an intensity of 1.5 W\u002Fcm² in continuous mode for 5 minutes. In the control group, a sham ultrasound procedure will be performed using the same device and duration without delivering therapeutic energy. Both the participants and the outcome assessor will be blinded to group allocation.\n\nVertical jump performance will be evaluated using the countermovement jump (CMJ) test recorded with the My Jump 2 smartphone application. In addition, quadriceps muscle strength will be measured using a hand-held dynamometer, and knee joint position sense will be assessed using a joint position reproduction test. All measurements will be conducted before and immediately after the intervention.\n\nThis study will provide evidence regarding whether therapeutic ultrasound applied to the patellar tendon can acutely influence explosive performance, muscle strength, and proprioception in healthy individuals.",[88],"Muscle Performance",[90,91,92,93,94],"Therapeutic Ultrasound","Patellar Tendon","Countermovement Jump","Acute Effect","Performance","2026-03-27",{"date":97,"type":36},"2026-04-02",{"date":99,"type":21},"2026-04-20",{"date":101,"type":21},"2026-05-01",{"name":42,"class":43},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":110,"targetDuration":4,"studyType":22,"phases":112,"briefSummary":113,"conditions":114,"keywords":116,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":44},"100623483","oropharyngeal-humidification-after-extubation-on-thirst-100623483","NCT07397221","Oropharyngeal Humidification After Extubation on Thirst","The Effect of Oropharyngeal Humidification After Extubation on Thirst, Pain, and Anxiety in Patients Undergoing Coronary Artery Bypass Surgery: A Randomized Controlled Study","Inclusion Criteria:\n\n* Age 18-65\n* Undergoing coronary artery bypass surgery\n* Postoperative mechanical ventilation and extubation\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Neuromuscular diseases (e.g., stroke, Parkinson's disease)\n* Head\u002Fneck deformities\n* Pre-existing dysphagia\n* Tracheostomy\n* Inability to participate in assessments",{"count":111,"type":21},42,[24],"In patients who have undergone endotracheal intubation following cardiac surgery, symptoms such as thirst, dysphagia (difficulty swallowing), restlessness, nausea, and vomiting are frequently observed, and these conditions negatively affect the patients' overall comfort. Especially in the post-intubation period, dryness in the mouth and throat, an intense feeling of thirst, and difficulty swallowing can lead to feelings of suffocation, helplessness, fear, and anxiety in patients. Effective management of these symptoms is critically important both for accelerating the recovery process and for increasing patient satisfaction.\n\nTraditionally, methods such as moistening the mouth with a cotton swab have been used to relieve complaints like thirst and dry mouth. However, these practices are often insufficient and have limited effectiveness in increasing patients' comfort. In recent years, the use of oropharyngeal sprays has emerged as an innovative and effective approach to alleviate symptoms such as thirst and dry mouth. In a randomized controlled trial conduct, it was shown that a spray-based oropharyngeal moisturizing program significantly reduced the severity of thirst and discomfort in patients who underwent intubation after cardiac surgery. Thirst and discomfort scores were found to be significantly lower in the spray-applied groups compared to the control group, and no significant difference was observed between the groups in terms of dysphagia frequency or adverse events. Similarly, studies conducted in different surgical and intensive care populations have shown that applications of cold water or cold saline sprays significantly reduce complaints of thirst and dry mouth, increase patient comfort, and are safe to use.\n\nAdditionally, it has been reported that alternative approaches such as menthol lozenges or aromatherapy also have positive effects on thirst, nausea, and comfort after cardiac surgery. Examining the effects of oropharyngeal sprays and similar practices on parameters such as thirst, dysphagia, discomfort, nausea, vomiting, and overall comfort in patients who are intubated after cardiac surgery may contribute to the development of innovative and effective approaches in patient care. Integrating such practices into postoperative care protocols carries significant potential for increasing patient comfort and supporting the recovery process.\n\nThis randomized controlled study aims to investigate the effects of oropharyngeal humidification after extubation on thirst, pain, and anxiety in patients undergoing coronary artery bypass surgery.",[115],"Coronary Artery Bypass",[117,118,27,119],"Oropharyngeal Humidification","Thirst","Coronary Artery Bypass Surgery","2026-02-09",{"date":122,"type":36},"2026-02-11",{"date":124,"type":21},"2026-02-01",{"date":126,"type":21},"2026-08-01",{"name":42,"class":43},{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":135,"minAge":17,"maxAge":4,"enrollmentInfo":136,"targetDuration":4,"studyType":22,"phases":137,"briefSummary":138,"conditions":139,"keywords":144,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":149,"lastUpdatePostDateStruct":150,"startDateStruct":152,"completionDateStruct":154,"leadSponsor":156,"locationsCount":4},"100620255","self-affirmation-intervention-after-mastectomy-100620255","NCT07355244","Self-Affirmation Intervention After Mastectomy","The Effect of Self-Affirmation Skills on Pain, Depression, Anxiety, and Stress in Patients Undergoing Mastectomy: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age 18 years or older\n* Female patients who have undergone mastectomy surgery\n* Able to speak and understand Turkish\n* Provides informed consent and agrees to participate voluntarily\n\nExclusion Criteria:\n\n* Diagnosed psychiatric disorder\n* Hearing impairment that prevents listening to the audio intervention","FEMALE",{"count":111,"type":21},[24],"This randomized controlled trial aims to evaluate the effect of a structured self-affirmation intervention on pain, depression, anxiety, and stress levels in patients undergoing mastectomy. The study will be conducted in two parallel groups, with the intervention group listening to an audio recording of positive self-affirmation statements. Primary outcomes will be assessed using the Visual Analog Scale and the Depression Anxiety Stress Scale (DASS-21). The goal is to provide evidence-based strategies to reduce psychosocial burden after mastectomy.",[140,141,27,142,143],"Breast Neoplasms","Mastectomy; Lymphedema","Depression","Stress, Psychological",[145,146,147,148,142],"Mastectomy","Breast Cancer","Stress","Anxiety","2026-01-12",{"date":151,"type":36},"2026-01-21",{"date":153,"type":21},"2026-01-01",{"date":155,"type":21},"2026-12-01",{"name":42,"class":43},{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":81,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":163,"targetDuration":4,"studyType":22,"phases":165,"briefSummary":166,"conditions":167,"keywords":171,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":176,"lastUpdatePostDateStruct":177,"startDateStruct":179,"completionDateStruct":181,"leadSponsor":183,"locationsCount":44},"100604059","the-effects-of-a-solution-focused-approach-on-psychosocial-adjustment-and-treatment-compliance-in-individuals-diagnosed-with-schizophrenia-100604059","NCT07144592","The Effects of a Solution-Focused Approach on Psychosocial Adjustment and Treatment Compliance in Individuals Diagnosed With Schizophrenia","Inclusion Criteria:\n\n* Having been diagnosed with schizophrenia according to DSM-5 diagnostic criteria,\n\nBeing between 18 and 65 years of age,\n\nBeing literate and verbally communicative,\n\nBeing clinically stable (not exhibiting symptoms of acute psychosis),\n\nBeing registered with a Community Mental Health Center (CMHC) and receiving regular services,\n\nBeing cognitively competent enough to participate in individual interviews during the research process,\n\nBeing an individual currently receiving psychiatric treatment and taking medication,\n\nAgreeing to participate voluntarily in the study and signing a written informed consent form.\n\nExclusion Criteria:\n\n* those who do not meet the inclusion criteria",{"count":164,"type":21},60,[24],"The aim of this study is to evaluate the effects of a solution-focused approach-based individual intervention on psychosocial adjustment and treatment adherence in individuals diagnosed with schizophrenia.\n\nThe study will be conducted as a randomized controlled trial including 60 clinically stable individuals diagnosed with schizophrenia according to DSM-5 criteria and registered at a Community Mental Health Center affiliated with a university hospital. Participants will be randomly assigned to an experimental group (n=30) and a control group (n=30).\n\nThe experimental group will receive one individual solution-focused therapy session per week for six weeks. The control group will receive usual care only. Data will be collected using a Personal Information Form, the Psychosocial Adjustment Scale (PSSAS), and the Medication Adherence Scale (MARS).",[168,169,170],"SCHIZOPHRENIA 1 (Disorder)","Psychosocial Adaptation","Treatment Adherence",[172,173,174,175],"treatment adherence","Schizophrenia","solution-focused therapy,","psychiatric nursing","2025-08-20",{"date":178,"type":36},"2025-08-27",{"date":180,"type":36},"2025-01-01",{"date":182,"type":21},"2025-10-25",{"name":42,"class":43},{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":4,"eligibilityCriteria":190,"healthyVolunteers":11,"sex":16,"minAge":191,"maxAge":192,"enrollmentInfo":193,"targetDuration":4,"studyType":22,"phases":195,"briefSummary":196,"conditions":197,"keywords":201,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":205,"lastUpdatePostDateStruct":206,"startDateStruct":208,"completionDateStruct":210,"leadSponsor":212,"locationsCount":44},"100590792","motivational-interviewing-based-training-100590792","NCT06972030","Motivational Interviewing-Based Training","The Effect of Motivational Interviewing-Based Training on Peer Bullying, Social Exclusion and Aggression in Secondary School Students","Inclusion Criteria:\n\n* Being 12-13 years old\n* Being in one of the 6th and 7th grades of middle school\n* Having a high score on the ''Peer Bullying Determination Scale''\n* Being willing to participate in the research\n* Not having a communication barrier\n* The student and their parents having signed the informed consent form.\n\nExclusion Criteria:\n\n* Having a low score on the ''Peer Bullying Determination Scale''\n* The volunteer not wanting to continue during the research\n* Encountering any communication barriers during the research\n* Answering the data collection forms incompletely or incorrectly","12 Years","13 Years",{"count":194,"type":21},80,[24],"The middle school period is the period when children begin to experience physical, emotional and social development and try to adapt to psychological changes. In this age group, which is seen as a transition period, the child's academic success and acceptance by peers and friends are also important. The problems experienced during this period can continue in adulthood and children are more likely to experience loneliness, sleep disorders, depression, anxiety, eating disorders, low self-esteem, suicidal thoughts, absenteeism and a decrease in academic success. For this reason, early detection of risky behaviors that threaten children's health and evaluation of health promotion practices are very important issues for child health nursing.\n\nIn recent years, peer bullying, aggression and social exclusion have increased and continue to increase in the middle school period, also called early adolescence. For this purpose, a study was needed to identify the situation in middle school students and reduce this negativity. In this respect, it is thought that the study will contribute to the literature. In addition, if the hypotheses of the study are confirmed, it is expected that similar training will be provided in other schools and contribute to the reduction of risky behaviors.\n\nThe aim of this study is to determine the effects of motivational interviewing-based education on peer bullying, social exclusion and aggression in secondary school students and to offer suggestions for situations where deficiencies are observed based on the findings obtained.",[198,199,200],"Social Exclusion","Aggression","Bullying of Child",[202,199,203,204],"Peer bullying","Social exclusion","Motivational interviewing","2025-05-16",{"date":207,"type":36},"2025-05-21",{"date":209,"type":21},"2025-09-01",{"date":211,"type":21},"2026-06-15",{"name":42,"class":43},{"id":214,"slug":215,"hasResults":11,"nctId":216,"briefTitle":217,"officialTitle":218,"acronym":4,"eligibilityCriteria":219,"healthyVolunteers":81,"sex":16,"minAge":52,"maxAge":220,"enrollmentInfo":221,"targetDuration":4,"studyType":22,"phases":223,"briefSummary":224,"conditions":225,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":228,"startDateStruct":230,"completionDateStruct":232,"leadSponsor":234,"locationsCount":44},"100590206","the-effect-of-reminiscence-therapy-in-elderly-100590206","NCT06964399","The Effect of Reminiscence Therapy in Elderly","Psychological Well-Being and Mindfulness in the Elderly: The Effect of Reminiscence Therapy","Inclusion Criteria:\n\n* Being over 65 years old\n* not having any serious psychiatric disorders\n* not having any diseases such as dementia etc.\n\nExclusion Criteria:\n\n* Having a serious psychiatric disorder\n* Not being able to attend sessions during the research process","100 Years",{"count":222,"type":21},90,[24],"In this study titled \"Psychological Well-Being and Awareness in the Elderly: The Effect of Reminiscence Therapy\", patients will be randomly divided into two groups as experimental and control groups. No intervention will be made to the patients in the control group. Reminiscence therapy will be applied to the patients in the experimental group. Participants will be asked to fill out the scale forms after accepting to participate in the study and obtaining their consent. In addition, after the reminiscence therapy is completed, the experimental and control groups will be asked to fill out the post-test forms.\n\nThe following questions will be answered in the study;\n\n* Does reminiscence therapy affect the psychological well-being levels of the elderly?\n* Does reminiscence therapy affect the awareness levels of the elderly?",[226],"Age-related Cognitive Decline","2025-05-07",{"date":229,"type":36},"2025-05-09",{"date":231,"type":36},"2025-04-01",{"date":233,"type":21},"2025-06-30",{"name":42,"class":43},{"id":236,"slug":237,"hasResults":11,"nctId":238,"briefTitle":239,"officialTitle":240,"acronym":4,"eligibilityCriteria":241,"healthyVolunteers":81,"sex":16,"minAge":52,"maxAge":220,"enrollmentInfo":242,"targetDuration":4,"studyType":22,"phases":243,"briefSummary":244,"conditions":245,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":248,"startDateStruct":249,"completionDateStruct":250,"leadSponsor":252,"locationsCount":44},"100590185","psycho-social-effects-of-gardening-activities-in-the-elderly-100590185","NCT06964126","Psycho-Social Effects of Gardening Activities in the Elderly","\"Psycho-Social Effects of Gardening Activities in the Elderly: An Investigation on Self-Esteem and Life Satisfaction","Inclusion Criteria:\n\n* The elderly who have a Standardized Mini Mental Test score of 24 and above,\n* Do not have vision or hearing loss that may prevent gardening activities,\n* Are open to communication and cooperation,\n* Volunteer to participate in the study will be included in the study.\n\nExclusion Criteria:\n\n* Having a communication problem\n* Having attended a gardening training in the last 6 months\n* Having a physical illness that would prevent gardening activities\n* Having a psychiatric illness that would prevent gardening activities will be excluded from the study.",{"count":222,"type":21},[24],"In this study titled \"Psycho-Social Effects of Gardening Activities in the Elderly: A Study on Self-Esteem and Life Satisfaction\", the elderly will be divided into two groups as experimental and control groups. Participants will be randomly assigned to the groups. No intervention will be made to the patients in the control group. Gardening activities will be performed on the patients in the experimental group as of April. The following questions will be answered in this study;\n\nDo gardening activities affect the self-esteem level of the elderly? Do gardening activities affect the life satisfaction level of the elderly?",[246,247],"Life Satisfaction","Self Esteem",{"date":229,"type":36},{"date":231,"type":36},{"date":251,"type":21},"2025-08-30",{"name":42,"class":43},{"id":254,"slug":255,"hasResults":11,"nctId":256,"briefTitle":257,"officialTitle":258,"acronym":4,"eligibilityCriteria":259,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":220,"enrollmentInfo":260,"targetDuration":4,"studyType":22,"phases":262,"briefSummary":263,"conditions":264,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":266,"lastUpdatePostDateStruct":267,"startDateStruct":269,"completionDateStruct":270,"leadSponsor":272,"locationsCount":44},"100585295","the-effect-of-sleep-hygiene-training-given-to-heart-failure-patients-on-their-hospitalacquired-insomnia-level-100585295","NCT06900504","\"The Effect of Sleep Hygiene Training Given to Heart Failure Patients on Their HospitalAcquired Insomnia Level\"","\"The Effect of Sleep Hygiene Training Given to Heart Failure Patients on Their HospitalAcquired Insomnia Level\": Randomized Controlled Trial","Inclusion Criteria:\n\n* Being over 18 years old\n* Being literate\n* Being a heart failure patient\n* Being hospitalized for at least 1 week and staying for another week\n* Not having a condition that prevents verbal communication\n* Not having a diagnosed psychiatric problem\n* Being a volunteer to participate in the research\n\nExclusion Criteria:\n\n* Having a verbal communication disability\n* Having a diagnosed psychiatric problem",{"count":261,"type":21},34,[24],"The purpose of this study is to examine the effect of sleep hygiene education given to heart failure patients on the level of hospital-acquired insomnia of the patients. Participants will be randomly assigned to groups as experimental and control groups. Standard application procedure will be applied to the control group. Sleep hygiene education will be given to the experimental group.\n\nResearch Hypotheses H0: Sleep hygiene education given to heart failure patients does not have a positive effect on the level of hospital-acquired insomnia of the patients.\n\nH1: Sleep hygiene education given to heart failure patients has a positive effect on the level of hospital-acquired insomnia of the patients.",[265],"Heart Failure","2025-03-23",{"date":268,"type":36},"2025-03-28",{"date":233,"type":21},{"date":271,"type":21},"2026-05-30",{"name":42,"class":43},{"id":274,"slug":275,"hasResults":11,"nctId":276,"briefTitle":277,"officialTitle":278,"acronym":4,"eligibilityCriteria":279,"healthyVolunteers":81,"sex":16,"minAge":17,"maxAge":220,"enrollmentInfo":280,"targetDuration":4,"studyType":22,"phases":281,"briefSummary":282,"conditions":283,"keywords":285,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":266,"lastUpdatePostDateStruct":287,"startDateStruct":288,"completionDateStruct":290,"leadSponsor":292,"locationsCount":44},"100585337","effect-of-fast-hugs-with-icu-approach-on-length-of-intensive-care-unit-stay-in-patients-with-hypoxic-respiratory-failure-100585337","NCT06901050","Effect of FAST HUGS WITH ICU Approach on Length of Intensive Care Unit Stay in Patients With Hypoxic Respiratory Failure","Effect of FAST HUGS WITH ICU Approach on Length of Intensive Care Unit Stay in Patients With Hypoxic Respiratory Failure: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Being over 18 years old\n* Being in the Chest Intensive Care Unit\n* Having Hypoxic Respiratory Failure\n\nExclusion Criteria:\n\n* Death during hospitalization",{"count":261,"type":21},[24],"This study will investigate the effect of the FAST HUGS WITH ICU approach on the length of stay in the intensive care unit in patients with hypoxic respiratory failure. Patients will be randomly assigned to the experimental and control groups. The standard procedure will be applied to the control group. The FAST HUGS WITH ICU approach will be applied to the experimental group. We plan to follow up patients with Hypoxic Respiratory Failure using the abbreviation FAST HUGS WITH ICU (Feeding, Analgesia, Sedation, Thromboembolic prophylaxis, Head of bed elevation, Stress Ulcer prophylaxis and Glucose control Spontaneous breathing trial, Water Balance and constipation, Investigation and results, Therapy, Hypo-hyper delirium, Invasive devices, Check the daily infection parameters, Use a checlist). The two groups will be examined in terms of hospital stay and some blood gas parameters.",[284],"Hypoxic Respiratory Failure",[286],"Hypoxic respiratory failure",{"date":268,"type":36},{"date":289,"type":36},"2024-12-01",{"date":291,"type":21},"2025-04-30",{"name":42,"class":43},{"id":294,"slug":295,"hasResults":11,"nctId":296,"briefTitle":297,"officialTitle":298,"acronym":4,"eligibilityCriteria":299,"healthyVolunteers":81,"sex":16,"minAge":17,"maxAge":300,"enrollmentInfo":301,"targetDuration":4,"studyType":22,"phases":302,"briefSummary":303,"conditions":304,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":307,"lastUpdatePostDateStruct":308,"startDateStruct":310,"completionDateStruct":312,"leadSponsor":314,"locationsCount":44},"100582164","does-educatonal-escape-game-affect-students-motvaton-academc-self-effcacy-and-success-levels-a-quas-expermental-study-100582164","NCT06859749","Does educatıonal Escape Game Affect Students' motıvatıon, academıc Self-effıcacy and Success Levels: a quası-experımental Study","Does educatıonal Escape Game Affect Students' motıvatıon, academıc Self-effıcacy and Success Levels","Inclusion Criteria:\n\n* Being over 18 years of age,\n* Receiving education in an elderly care program,\n* Not having previously taken the \"Elderly Care Principles and Practices I\" and \"Elderly Care Principles and Practices II\" courses,\n* Providing attendance during data collection processes.\n* Having a phone and internet that can enter Google forms.\n\nExclusion Criteria:\n\n* Being under 18 years of age,\n* Not cooperating,\n* Having previously taken the \"Elderly Care Principles and Practices I\" and \"Elderly Care Principles and Practices II\" courses,\n* Being absent.","50 Years",{"count":20,"type":21},[24],"This is a semi-experimental study. The study aimed to examine the effects of an educational escape game on students' motivation, academic self-efficacy and achievement levels. Students studying in an elderly care program will be included in the study. Students will be divided into 2 groups according to their branches: experimental (educational escape game) and control (question-answer).\n\nH1. Students participating in the escape game will show significantly higher motivation in the \"Motivation Scale for Teaching Materials\" than students participating in the question-answer method.\n\nH2. Students participating in the escape game will show significantly higher self-efficacy in the \"Academic Self-Efficacy Scale\" than students participating in the question-answer method.\n\nH3. Students participating in the escape game will show significantly higher success in the \"Achievement Test\" than students participating in the question-answer method.",[305,306],"Motivation","Self Efficacy","2025-03-04",{"date":309,"type":36},"2025-03-05",{"date":311,"type":36},"2024-11-01",{"date":313,"type":21},"2025-03-20",{"name":42,"class":43},{"id":316,"slug":317,"hasResults":11,"nctId":318,"briefTitle":319,"officialTitle":320,"acronym":4,"eligibilityCriteria":321,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":322,"targetDuration":4,"studyType":22,"phases":324,"briefSummary":325,"conditions":326,"keywords":328,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":330,"lastUpdatePostDateStruct":331,"startDateStruct":333,"completionDateStruct":335,"leadSponsor":337,"locationsCount":4},"100569170","relaxation-exercise-and-education-in-patients-with-irritable-bowel-syndrome-100569170","NCT06690762","Relaxation Exercise and Education in Patients With Irritable Bowel Syndrome","The Effect of Mobile Technology-Based Education Combined With Relaxation Exercise on Stress, Symptom Severity and Quality of Life in Patients With Irritable Bowel Syndrome.","Inclusion Criteria:\n\n* 18 years of age and older, applied to the polyclinic where the study was conducted,\n* Have been diagnosed with IBS according to Rome IV criteria,\n* Have a smart phone or computer,\n* Have no illness that would prevent them from doing progressive muscle relaxation exercises (heart failure, chronic obstructive pulmonary disease, asthma, pregnant, etc.),\n\nExclusion Criteria:\n\n* Having communication problems",{"count":323,"type":21},100,[24],"Irritable bowel syndrome (IBS) is a common functional gastrointestinal disorder characterized by chronic recurrent abdominal pain, bloating, changes in bowel habits or bowel movements (1-3). Pharmacological and nonpharmacological methods are used in the treatment of IBS. In addition to lifestyle changes such as dietary changes, physical activity, and stress reduction, relaxation techniques, herbal medicines, and nutritional supplements are important nonpharmacological methods used by IBS patients.\n\nProgressive muscle relaxation exercises (PGE) have been reported to positively affect IBS symptoms, patients' quality of life, anxiety, and depression. PGE training in patients with IBS has been found to improve general health perception, reduce symptom severity, and healthcare costs. (7-9). PGE is a complementary treatment and is among advanced nursing practices (10, 11).\n\nIn this study, a mobile application will be developed to educate patients about IBS and PGE. It is thought that this application will reduce the severity of patients' symptoms and increase their quality of life. This study is planned to determine the effects of mobile technology-based training combined with relaxation exercises on stress, symptom severity and quality of life in patients with irritable bowel syndrome.",[327],"Irritable Bowel Disease",[329],"Irritable Bowel Syndrome, Stress, Symptom Severity, Quality of Life, Relaxation","2024-11-13",{"date":332,"type":36},"2024-11-15",{"date":334,"type":21},"2024-12-02",{"date":336,"type":21},"2025-07-22",{"name":42,"class":43},{"id":339,"slug":340,"hasResults":11,"nctId":341,"briefTitle":342,"officialTitle":342,"acronym":4,"eligibilityCriteria":343,"healthyVolunteers":11,"sex":135,"minAge":344,"maxAge":52,"enrollmentInfo":345,"targetDuration":4,"studyType":347,"phases":4,"briefSummary":348,"conditions":349,"keywords":351,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":356,"lastUpdatePostDateStruct":357,"startDateStruct":359,"completionDateStruct":361,"leadSponsor":363,"locationsCount":4},"100564891","the-relationship-between-education-status-and-care-burden-of-mothers-of-individuals-with-cerebral-palsy-100564891","NCT06635070","The Relationship Between Education Status and Care Burden of Mothers of Individuals With Cerebral Palsy","Inclusion Criteria:\n\n* Having a child who is receiving education in special education institutions\n* The child's diagnosis was made at least 6 months ago\n* The disabled individuals must be between the ages of 0-18\n\nExclusion Criteria:\n\n\\-","20 Years",{"count":346,"type":21},120,"OBSERVATIONAL","This study, examines how maternal education affects caregiving burdens for children with cerebral palsy. Cerebral palsy requires long-term, intensive care, often leading to significant physical, emotional, and financial strain on caregivers. The study aims to assess whether higher maternal education is associated with lower care burdens, possibly due to increased access to resources or coping strategies, and whether lower educational levels result in greater challenges. A survey, combined with standardized measures such as the Caregiver Burden Scale, will be used to quantify the caregiving burden. The results are expected to inform policies or interventions aimed at reducing caregiver strain.",[350],"Cerebral Palsy",[352,353,354,355],"Cerebral palsy","Caregiver Burden","Mother","Educational Status","2024-10-09",{"date":358,"type":36},"2024-10-10",{"date":360,"type":21},"2024-10-21",{"date":362,"type":21},"2024-12-16",{"name":42,"class":43},{"id":365,"slug":366,"hasResults":11,"nctId":367,"briefTitle":368,"officialTitle":368,"acronym":4,"eligibilityCriteria":369,"healthyVolunteers":81,"sex":16,"minAge":370,"maxAge":371,"enrollmentInfo":372,"targetDuration":4,"studyType":347,"phases":4,"briefSummary":374,"conditions":375,"keywords":377,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":382,"lastUpdatePostDateStruct":383,"startDateStruct":384,"completionDateStruct":385,"leadSponsor":386,"locationsCount":4},"100564718","the-relationship-between-health-literacy-physical-activity-back-pain-and-posture-habits-in-university-students-100564718","NCT06632821","The Relationship Between Health Literacy, Physical Activity, Back Pain and Posture Habits in University Students","Inclusion Criteria:\n\n* Being a university student\n\nExclusion Criteria:\n\n* Having any diagnosed physical or psychological illness","17 Years","19 Years",{"count":373,"type":21},500,"This study aims to investigate the relationship between health literacy, physical activity, back pain, and posture habits among university students. The Health Literacy Scale, the International Physical Activity Questionnaire, and the Posture Habits Questionnaire for Back Health in Daily Activities will be used to collect data from participants. Health literacy will be assessed in terms of individuals' ability to access, understand, and apply health-related information, while physical activity levels and posture habits will be examined for their influence on back pain. The findings are expected to shed light on the role of health literacy in promoting healthier physical activity and posture habits, providing insights for strategies to improve back health in this population.",[376],"University Students",[378,379,380,381],"university students","physical activity","back pain","posture habits","2024-10-08",{"date":356,"type":36},{"date":360,"type":21},{"date":362,"type":21},{"name":42,"class":43},{"id":388,"slug":389,"hasResults":11,"nctId":390,"briefTitle":391,"officialTitle":392,"acronym":393,"eligibilityCriteria":394,"healthyVolunteers":81,"sex":16,"minAge":17,"maxAge":300,"enrollmentInfo":395,"targetDuration":4,"studyType":22,"phases":396,"briefSummary":397,"conditions":398,"keywords":400,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":404,"lastUpdatePostDateStruct":405,"startDateStruct":406,"completionDateStruct":408,"leadSponsor":410,"locationsCount":4},"100564717","effectiveness-of-deep-cervical-flexor-muscle-exercises-in-patients-with-tension-type-headache-100564717","NCT06632808","Effectiveness of Deep Cervical Flexor Muscle Exercises in Patients With Tension-Type Headache","Effects of Deep Cervical Flexor Muscle Exercises on Pain, Spinal Posture, and Sensory Sensitivity in Patients With Tension-Type Headache: A Single-Blind Randomized Controlled Trial","Single-Blind","Inclusion Criteria:\n\n* being diagnosed with tension-type headache\n\nExclusion Criteria:\n\n* whiplash injury,\n* significant neck trauma (caused by trauma to the neck, fracture, distortion, or violent attack that have caused the current NP),\n* nerve root compression of the cervical spine,\n* persistent headache attributed to traumatic injury to the head\n* cluster headache,\n* trigeminal neuralgia,\n* pregnancy,\n* breastfeeding,\n* severe physical and\u002For mental illness",{"count":84,"type":21},[24],"The aim of this study is to evaluate the effects of deep cervical flexor muscle exercises on pain, spinal posture, and sensory sensitivity in patients with tension-type headaches. Designed as a single-blind randomized controlled trial, the study will assess participants' pain levels using the Visual Analog Scale (VAS), sensory sensitivity through the Sensory Sensitivity Scale, and spinal posture via a digital inclinometer for objective measurements. This research seeks to determine the effectiveness of these exercises in managing pain, improving spinal posture, and contributing to the enhancement of sensory sensitivity.",[399],"Tension-Type Headache",[401,27,402,403],"Tension-type headache","Posture","sensory sensitivity","2024-10-07",{"date":356,"type":36},{"date":407,"type":21},"2024-11-18",{"date":409,"type":21},"2025-01-31",{"name":42,"class":43},{"id":412,"slug":413,"hasResults":11,"nctId":414,"briefTitle":415,"officialTitle":415,"acronym":4,"eligibilityCriteria":416,"healthyVolunteers":11,"sex":16,"minAge":370,"maxAge":371,"enrollmentInfo":417,"targetDuration":418,"studyType":347,"phases":4,"briefSummary":419,"conditions":420,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":404,"lastUpdatePostDateStruct":421,"startDateStruct":422,"completionDateStruct":423,"leadSponsor":424,"locationsCount":4},"100564716","the-relationship-between-emotional-intelligence-social-behavior-sleep-quality-and-academic-success-in-students-studying-in-health-related-departments-100564716","NCT06632795","The Relationship Between Emotional Intelligence, Social Behavior, Sleep Quality and Academic Success in Students Studying in Health-Related Departments","Inclusion Criteria:\n\n* Being a university student in health-related departments\n\nExclusion Criteria:\n\n* Having any diagnosed physical or psychological illness",{"count":373,"type":21},"2 Months","This study aims to examine the relationships between emotional intelligence, positive social behavior, sleep quality, and academic achievement among students enrolled in health-related academic programs. Specifically, the study will investigate how emotional intelligence levels influence students' social behaviors and academic performance, while also assessing the role of sleep quality in these variables. Data will be collected using the Emotional Intelligence Scale, the Positive Social Behavior Scale, and the Epworth Sleepiness Scale. The findings of this study are expected to provide valuable insights into how emotional intelligence and sleep quality impact students' academic success and social behavior.",[376],{"date":356,"type":36},{"date":360,"type":21},{"date":362,"type":21},{"name":42,"class":43},{"id":426,"slug":427,"hasResults":11,"nctId":428,"briefTitle":429,"officialTitle":430,"acronym":4,"eligibilityCriteria":431,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":432,"targetDuration":4,"studyType":22,"phases":433,"briefSummary":434,"conditions":435,"keywords":438,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":444,"lastUpdatePostDateStruct":445,"startDateStruct":447,"completionDateStruct":449,"leadSponsor":450,"locationsCount":4},"100556983","effects-of-su-jok-therapy-on-pain-fatigue-nausea-vomiting-and-spiritual-well-being-100556983","NCT06532201","Effects of Su Jok Therapy on Pain, Fatigue, Nausea-Vomiting and Spiritual Well-Being","Effects of Su Jok Therapy on Pain, Fatigue, Nausea-Vomiting and Spiritual Well-Being Levels in Patients Receiving Chemotherapy","Inclusion Criteria:\n\n* Being over 18 years old\n* Being diagnosed with cancer\n* Being receiving chemotherapy\n* No communication problems\n\nExclusion Criteria:\n\n* Deterioration or death during the research process\n* Requesting to withdraw from the research\n* Incomplete filling of forms",{"count":20,"type":21},[24],"This study aims to examine the effects of sujok therapy on pain, fatigue, nausea-vomiting and spiritual well-being levels in patients receiving chemotherapy. The following questions are being answered;\n\n* Does sujok therapy affect pain levels in cancer patients?\n* Does sujok therapy affect fatigue levels in cancer patients?\n* Does sujok therapy affect nausea-vomiting levels in cancer patients?\n* Does sujok therapy affect spiritual well-being levels in cancer patients?",[436,437],"Cancer","Chemotherapy",[439,440,27,441,442,443],"su-jok","cancer patients","fatigue","nausea-vomiting","spiritual well-being","2024-07-29",{"date":446,"type":36},"2024-08-01",{"date":448,"type":21},"2024-10-01",{"date":180,"type":21},{"name":42,"class":43},{"id":452,"slug":453,"hasResults":11,"nctId":454,"briefTitle":455,"officialTitle":455,"acronym":4,"eligibilityCriteria":456,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":457,"targetDuration":4,"studyType":22,"phases":458,"briefSummary":459,"conditions":460,"keywords":462,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":444,"lastUpdatePostDateStruct":465,"startDateStruct":466,"completionDateStruct":467,"leadSponsor":468,"locationsCount":4},"100556981","effects-of-su-jok-seed-therapy-application-on-pain-anxiety-and-psychological-resilience-in-patients-hospitalized-in-the-oncology-ward-100556981","NCT06532175","Effects of Su Jok Seed Therapy Application on Pain, Anxiety and Psychological Resilience in Patients Hospitalized in the Oncology Ward","Inclusion Criteria:\n\n* Being over 18 years old,\n* No communication problems,\n* Individuals diagnosed with cancer\n\nExclusion Criteria:\n\n* Getting worse or dying during the research process",{"count":194,"type":21},[24],"The aim of this clinical trial is to determine the effects of su jok seed therapy on pain, anxiety and psychological resilience in patients hospitalized in the oncology ward. This study seeks answers to the following questions; Does su jok seed therapy affect the pain levels of cancer patients? Does su jok seed therapy affect the anxiety levels of cancer patients? Does su jok seed therapy affect the Psychological resilience levels of cancer patients? There will be an experimental and control group in the study and the effectiveness of sujok application will be examined.\n\nA total of 8 sessions of su jok seed therapy will be applied to the experimental group, twice a week for a month. No intervention will be made to the control group.\n\nIndividuals over 18 years old, without communication problems and diagnosed with cancer will be included in the sample.",[436,461],"Cancer Pain",[439,440,463,29,464],"anxiety","Psychological resilience",{"date":446,"type":36},{"date":446,"type":21},{"date":448,"type":21},{"name":42,"class":43},""]