[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of Yalova\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":379},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,14,0,[8,49,79,106,128,155,182,209,239,263,288,310,336,356],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100053389","training-on-the-heimlich-maneuver-for-mothers-of-children-with-disabilities-100053389",false,"NCT07699341","Training on the Heimlich Maneuver for Mothers of Children With Disabilities","For a Safe Breath: Training on the Heimlich Maneuver for Mothers of Children With Disabilities in Cases of Foreign Body Obstruction","Inclusion Criteria:\n\n1. Be a mother of a child with a disability, aged 1-8, who is enrolled in a rehabilitation center.\n2. Be 18 years of age or older.\n3. Be able to read and understand the research protocol, provide written informed consent, and agree to participate.\n4. Be physically able to participate in the training (standing\u002Fmodel-based exercises).\n\nExclusion Criteria:\n\n1. Must have previously received professional Heimlich maneuver\u002Ffirst aid training (those who have taken a course within the last 2 years).\n2. Those who are unable to participate in hands-on training due to physical limitations (e.g., severe heart disease, mobility issues).\n3. Individuals determined to be unsuitable for training or assessments due to psychiatric or neurological conditions.\n4. Children with severe respiratory system disorders (e.g., tracheostomy, severe bronchopulmonary dysplasia),\n5. Children who have undergone heart surgery or have a serious cardiac anomaly,\n6. Children with severe orthopedic or neurological disabilities for whom performing the Heimlich maneuver may be risky,\n7. Children with congenital anomalies of the trachea or upper respiratory tract (e.g., tracheoesophageal fistula),\n8. Children requiring mechanical ventilator support or continuous oxygen therapy.\n9. Withdrawing from participation during the study or failing to attend any of the training\u002Ftesting sessions.",true,"FEMALE","18 Years",{"count":20,"type":21},70,"ESTIMATED","INTERVENTIONAL",[24],"NA","Foreign body obstruction is one of the most common causes of medical emergencies, particularly in childhood, and can lead to fatal outcomes if not treated promptly and correctly. Therefore, this study aims to examine the effect of hands-on Heimlich maneuver training for mothers of children with disabilities on the mothers' knowledge, skills, self-efficacy, and anxiety levels. Conducted as a randomized controlled trial, the study is planned to include 70 mothers (experimental group: 35, control group: 35) of children aged 1-8 years attending a private rehabilitation center in the Besni district of Adıyaman. Data collection tools will consist of a demographic information form, a Heimlich maneuver knowledge and skill test, and self-efficacy and anxiety scales. A pilot study will be conducted to evaluate the validity and reliability of the data collection tools, test their comprehensibility for the mothers, and identify potential problems that may arise during implementation. Prior to the start of the training, the knowledge levels of all mothers will be assessed via a questionnaire. The Heimlich maneuver training provided to mothers in the experimental group will be delivered hands-on using a pediatric Heimlich mannequin. One month after the training, a post-test will be administered to the mothers. Mothers in the control group will be informed about the study during the initial interview and will take a pre-test. One month after the training, the mothers will take the post-test. Mothers in the control group will be informed about the study during the initial interview and will take the pre-test. The post-test will be administered one month later, after which the mothers in this group will also receive maneuver training. The mothers' pre-test and post-test scores will be compared both within and between groups.",[27,28,29],"Disabilities Multiple","Obstruction Airway","Foreign Body Aspiration",[31,32,33,34,35],"Breath","Foreign Body Obstruction","Disabilities","Children","Heimlich Maneuver","RECRUITING","2026-07-09",{"date":39,"type":40},"2026-07-13","ACTUAL",{"date":42,"type":40},"2016-06-01",{"date":44,"type":21},"2026-11-30",{"name":46,"class":47},"University of Yalova","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":16,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":48},"100644518","blended-learning-for-psychosocial-nursing-diagnoses-100644518","NCT07670351","Blended Learning for Psychosocial Nursing Diagnoses","The Effect of Blended Learning Approach on Psychosocial Nursing Diagnoses in Nursing Students: A Randomized Controlled Study","Inclusion Criteria:\n\n* Being enrolled as a nursing student at the institution where the research is conducted\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n\\- Refusing to participate in the study","ALL",{"count":58,"type":21},52,[24],"The nursing process is a systematic approach forming the basis of professional nursing care. Literature indicates that nursing students experience the most difficulty in determining nursing diagnoses, often focusing predominantly on physical needs while neglecting psychosocial, social, and spiritual dimensions. This situation limits the effective implementation of holistic care. The purpose of this study is to evaluate the effect of a case-based blended learning approach developed for nursing students on their knowledge levels and skills in differentiating, correlating, and accurately expressing psychosocial nursing diagnoses. It is anticipated that the findings obtained will contribute to enriching the content of nursing curricula and improving instructional methods.",[62,63,64],"Nursing Diagnosis","Psychosocial Diagnoses","Psychosocial Care",[66,67,68,69,70],"Blended Learning","Nursing Students","Psychosocial Nursing Diagnoses","Interactive Video","Nursing Process","2026-06-24",{"date":73,"type":40},"2026-06-26",{"date":75,"type":40},"2026-06-09",{"date":77,"type":21},"2027-02",{"name":46,"class":47},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":16,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":89,"conditions":90,"keywords":95,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":4},"100644131","burden-of-care-and-health-literacy-of-caregivers-in-the-emergency-department-100644131","NCT07666373","Burden of Care and Health Literacy of Caregivers in the Emergency Department","The Relationship Between Caregiver Burden and Health Literacy Among Caregivers of Patients With Chronic Diseases Presenting to the Emergency Department","The patient having visited the Yalova Training and Research Hospital Emergency Department.\n\nBeing at least 18 years of age. Being cognitively capable of answering the data collection tools (scales\u002Fquestionnaires).\n\nVolunteering to participate in the study and providing informed consent.\n\nExclusion Criteria:\n\nRefusal to participate in the research voluntarily. Not being the primary caregiver for the patient. Inability to communicate or complete the scales due to cognitive or language barriers.\n\n\\-",{"count":87,"type":21},350,"OBSERVATIONAL","This study aims to investigate the relationship between caregiver burden and health literacy among primary caregivers of patients with chronic diseases presenting to the emergency department. The study will be conducted in the Emergency Department of Yalova Training and Research Hospital and will include at least 300 caregivers. Data will be collected using a sociodemographic questionnaire, the Turkish Health Literacy Scale-32 (THLS-32), and the Zarit Burden Interview (ZBI). The findings are expected to contribute to a better understanding of caregivers' needs and to clarify the role of health literacy in caregiver burden among those providing care for individuals with chronic illnesses.",[91,92,93,94],"Caregiver Burden","Health Literacy","Chronic Disease","Emergency Service Utilization",[91,92,96,97],"Family Caregivers","Emergency Service","NOT_YET_RECRUITING","2026-06-18",{"date":71,"type":40},{"date":102,"type":21},"2026-07-01",{"date":104,"type":21},"2027-05-31",{"name":46,"class":47},{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":110,"acronym":111,"eligibilityCriteria":112,"healthyVolunteers":11,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":113,"targetDuration":115,"studyType":88,"phases":4,"briefSummary":116,"conditions":117,"keywords":119,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":4},"100644007","outpatient-cancer-patients-the-relationship-between-information-overload-symptom-severity-and-empowerment-level-100644007","NCT07667881","OUTPATIENT CANCER PATIENTS: THE RELATIONSHIP BETWEEN INFORMATION OVERLOAD, SYMPTOM SEVERITY, AND EMPOWERMENT LEVEL","CANCER PATIENT","Inclusion Criteria: Eligibility criteria include having a clinical diagnosis of cancer, having received at least one course of outpatient chemotherapy, and being 18 years of age or older.\n\n\\-\n\nExclusion Criteria: The criteria for eligibility include having a severe mental disorder that could affect the patient's perception and responses, it being the first day of treatment, and the patient being under 18 years of age.\n\n\\-",{"count":114,"type":21},300,"3 Months","Examining the relationship between information load, symptom severity, and empowerment level in outpatient cancer patients is of great importance for developing holistic care plans tailored to the individual needs of patients and for planning supportive interventions in oncology nursing.",[118],"Oncologic Disease",[120],"cancer, information overload, symptom management, patient empowerment, nursing",{"date":122,"type":40},"2026-06-25",{"date":124,"type":21},"2026-07",{"date":126,"type":21},"2026-09",{"name":46,"class":47},{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":16,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":135,"targetDuration":4,"studyType":22,"phases":137,"briefSummary":138,"conditions":139,"keywords":146,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":152,"leadSponsor":154,"locationsCount":48},"100639995","the-effect-of-ai-assisted-nursing-process-training-on-nursing-process-competence-perception-and-attitudes-towards-artificial-intelligence-in-nurses-a-randomized-controlled-study-100639995","NCT07618975","The Effect of AI-Assisted Nursing Process Training on Nursing Process Competence, Perception and Attitudes Towards Artificial Intelligence in Nurses: A Randomized Controlled Study","Hemşirelerde Yapay Zeka Destekli Hemşirelik Süreci Eğitiminin Hemşirelik Süreci Yetkinliğine, Yapay Zeka Algı ve Tutumuna Etkisi: Randomize Kontrollü Bir Çalışma","Inclusion Criteria:\n\n* Volunteering to participate in the study.\n* Working actively as a nurse in the specified institution (Yalova Training and Research Hospital).\n* Not having previously used artificial intelligence in the nursing process.\n\nExclusion Criteria:\n\n* Refusing to participate in the study.\n* Having previously used artificial intelligence in the nursing process. Submitting incomplete data collection forms.\n* Requesting to withdraw from the study.",{"count":136,"type":21},78,[24],"This study aims to determine how applied artificial intelligence (AI) training affects nurses' ability to manage the nursing process and their perceptions and attitudes toward AI technology\n\n* The nursing process is a scientific, six-stage approach used by nurses to identify patient needs and provide holistic care\n\nThe research is a randomized controlled trial involving 78 nurses at Yalova Education and Research Hospital\n\n. Participants will be split into two groups: Both groups will receive standard theoretical training on the nursing process\n\n. The intervention group will receive additional specialized training on using AI tools (such as ChatGPT and Deepseek) to help create nursing care plans through practical case studies\n\n. Nurses' skills and views will be measured using specific scales before the training and one month after the intervention to evaluate the training's effectiveness\n\n* This study is expected to provide valuable insights into how AI can support clinical decision-making and help healthcare providers adapt to new technologies\n* The research has been approved by the Yalova University Ethics Committee (Protocol 2026\u002F183) and will be conducted between May and December 2026",[140,141,142,70,143,144,145],"Nursing Process Competence","Artificial Intelligence Perception and Attitude","Nursing Education","Artificial Intelligence","Clinical Competence","Artificial Intelligence (AI)",[143,70,142,144,147],"Attitude of Health Personnel","2026-05-24",{"date":150,"type":40},"2026-06-01",{"date":150,"type":21},{"date":153,"type":21},"2026-12-31",{"name":46,"class":47},{"id":156,"slug":157,"hasResults":11,"nctId":158,"briefTitle":159,"officialTitle":160,"acronym":161,"eligibilityCriteria":162,"healthyVolunteers":11,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":163,"targetDuration":4,"studyType":22,"phases":165,"briefSummary":166,"conditions":167,"keywords":169,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":48},"100637292","lying-positions-in-intramuscular-injection-100637292","NCT07586605","Lying Positions in Intramuscular Injection","The Effect of Three Different Lying Positions on Pain, Comfort, and Satisfaction Levels in Intramuscular Injection: A Randomized Controlled Trial","Lying","Inclusion Criteria:\n\n* Being 18 years of age or older,\n* Having received an IM injection at least one week prior to the study,\n* Absence of scars, ecchymosis, or hematomas at the injection site,\n* Having a BMI between 18.5 and 24.9 kg\u002Fm²,\n* Absence of lower extremity paralysis,\n* Not receiving any oral or parenteral analgesic treatment prior to the injection.\n\nExclusion Criteria:\n\n* Failure of the patient to respond to the questions in the post-procedure data collection form.",{"count":164,"type":21},111,[24],"The aim of this study is to examine the effects of intramuscular (IM) injections administered in three different lying positions (supine, prone, and lateral) into the ventrogluteal site on patient pain, comfort, and procedural satisfaction. The study will be conducted as a randomized controlled experimental trial with three groups. In Experimental Group 1, patients will be placed in the supine position; in Experimental Group 2, the lateral position; and in Experimental Group 3, the prone position prior to the injection procedure, followed by an IM injection into the ventrogluteal site. Subsequent to the procedure, patients' pain, comfort, and procedural satisfaction levels will be assessed.",[168],"Ventrogluteal Injections",[170,171,172,173],"intramuscular injection","lying position","pain","patient satisfaction","2026-05-19",{"date":176,"type":40},"2026-05-22",{"date":178,"type":21},"2026-04-30",{"date":180,"type":21},"2026-08-30",{"name":46,"class":47},{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":187,"acronym":188,"eligibilityCriteria":189,"healthyVolunteers":16,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":190,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":191,"conditions":192,"keywords":195,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":201,"lastUpdatePostDateStruct":202,"startDateStruct":204,"completionDateStruct":206,"leadSponsor":208,"locationsCount":4},"100639651","nursing-competency-scale-in-pressure-injury-prevention-a-scale-development-study-100639651","NCT07590765","NURSING COMPETENCY SCALE IN PRESSURE INJURY PREVENTION: A SCALE DEVELOPMENT STUDY","Nursing Competency Scale in Pressure Injury Prevention: A Scale Development Study","NCSPIP","Inclusion Criteria:\n\n* Working as a nurse in the related institution\n* Voluntarily agreeing to participate in the study\n* Being 18 years of age or older\n\nExclusion Criteria:\n\n* Not working as a nurse in the related institution\n* Not voluntarily agreeing to participate in the study\n* Incomplete completion of the data collection forms",{"count":114,"type":21},"Pressure injuries remain an important patient safety problem and are associated with prolonged hospitalization, increased healthcare costs, pain, and reduced quality of care. Nurses play a key role in the prevention of pressure injuries through risk assessment, skin care, positioning, nutritional management, and evidence-based preventive interventions.\n\nThe purpose of this study is to develop and evaluate the psychometric properties of the Nursing Competency Scale in Pressure Injury Prevention. The scale is intended to assess nurses' competencies regarding pressure injury prevention in line with updated international guidelines. The study will be conducted with nurses working in a training and research hospital in Türkiye.\n\nThe scale development process will include item generation, expert evaluation for content validity, pilot testing, exploratory factor analysis, confirmatory factor analysis, criterion validity, internal consistency analysis, and test-retest reliability assessment.",[193,194],"Pressure Injury","Nursing Competency",[193,196,194,197,198,199,200],"Pressure Injury Prevention","Scale Development","Psychometric Evaluation","Nurses","Medical Device-Related Pressure Injury","2026-05-10",{"date":203,"type":40},"2026-05-15",{"date":205,"type":21},"2026-05-20",{"date":207,"type":21},"2027-01-30",{"name":46,"class":47},{"id":210,"slug":211,"hasResults":11,"nctId":212,"briefTitle":213,"officialTitle":214,"acronym":4,"eligibilityCriteria":215,"healthyVolunteers":11,"sex":56,"minAge":216,"maxAge":4,"enrollmentInfo":217,"targetDuration":4,"studyType":22,"phases":219,"briefSummary":220,"conditions":221,"keywords":225,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":231,"lastUpdatePostDateStruct":232,"startDateStruct":234,"completionDateStruct":236,"leadSponsor":238,"locationsCount":4},"100635130","rehabilitation-interventions-after-cardiac-surgery-in-older-adults-100635130","NCT07548684","Rehabilitation Interventions After Cardiac Surgery in Older Adults","Rehabilitation Interventions After Cardiac Surgery in Older Adults: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age ≥65 years\n* Undergoing cardiac surgery (e.g., coronary artery bypass grafting or valve surgery)\n* Conscious and able to cooperate\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Presence of neurological disorders (e.g., stroke, Parkinson's disease)\n* Lower extremity amputation or severe deformity\n* Impaired skin integrity in the application area\n* Contraindications to massage or kinesio taping\n* Refusal to participate","65 Years",{"count":218,"type":21},60,[24],"This randomized controlled trial aims to investigate the effects of foot massage and kinesio taping on functional performance and kinesiophobia in older adults following cardiac surgery. Early mobilization after cardiac surgery is essential for improving recovery outcomes; however, pain, fear of movement (kinesiophobia), and reduced functional capacity may delay rehabilitation in older patients.\n\nParticipants aged 65 years and older who have undergone cardiac surgery will be randomly assigned to either a foot massage group or a kinesio taping group. The foot massage group will receive daily bilateral foot massage for seven consecutive days, while the kinesio taping group will receive standardized kinesio taping applications to the foot and ankle region during the same period.\n\nFunctional performance, kinesiophobia, pain intensity, cognitive status, and delirium will be assessed using validated outcome measures, including the Timed Up and Go test, Tampa Scale for Kinesiophobia, Visual Analog Scale, Standardized Mini-Mental Test, and Nursing Delirium Screening Scale. Assessments will be conducted preoperatively and on the seventh postoperative day.\n\nThe study aims to determine whether non-pharmacological, easily applicable interventions such as foot massage and kinesio taping can enhance functional recovery, reduce fear of movement, and support early mobilization in older adults after cardiac surgery.",[222,223,224],"Cardiac Surgery","Postoperative Rehabilitation","Kinesiophobia",[226,227,222,228,229,224,223,230],"Foot Massage","Kinesio Taping","Older Adults","Functional Performance","Early Mobilization","2026-04-23",{"date":233,"type":40},"2026-04-24",{"date":235,"type":21},"2026-05-01",{"date":237,"type":21},"2027-02-01",{"name":46,"class":47},{"id":240,"slug":241,"hasResults":11,"nctId":242,"briefTitle":243,"officialTitle":243,"acronym":4,"eligibilityCriteria":244,"healthyVolunteers":11,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":245,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":247,"conditions":248,"keywords":252,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":257,"lastUpdatePostDateStruct":258,"startDateStruct":259,"completionDateStruct":260,"leadSponsor":262,"locationsCount":48},"100634227","individualized-care-perceptions-of-patients-receiving-outpatient-chemotherapy-a-qualitative-study-100634227","NCT07536945","Individualized Care Perceptions of Patients Receiving Outpatient Chemotherapy: A Qualitative Study","Inclusion Criteria:\n\n* Continuing treatment at the Outpatient Chemotherapy Unit of the relevant hospital.\n* Voluntarily agreeing to participate in the study.\n* Being over 18 years of age.\n* Being proficient in Turkish.\n* Exclusion Criteria:\n* Not receiving ongoing treatment at the Outpatient Chemotherapy Unit of the relevant hospital.\n* Declining to participate in the study voluntarily.\n* Unwillingness to answer questions or lack of cooperation during the interview.",{"count":246,"type":21},10,"The purpose of this observational study is to learn how people receiving chemotherapy in a clinic without staying overnight (outpatient) feel about the care they receive. The study focuses on individualized care, which means nursing care that is tailored specifically to each person's unique needs, values, and lifestyle.\n\nBackground:\n\nCancer treatment often involves chemotherapy (medicine used to kill cancer cells). While these treatments help fight the disease, they can also cause side effects like nausea or tiredness, which affect daily life. Nurses play a key role in helping people manage these effects. This research aims to understand how \"individualized care\" helps participants feel valued and supported during their treatment journey.\n\nThe study aims to answer these key questions:\n\nHow do participants describe their experiences with nursing care?\n\nWhat are the specific needs and expectations of these individuals for care that feels personal to them?\n\nHow does personalized care affect their ability to manage symptoms and follow their treatment plan?\n\nScope and Setting:\n\nThis study will take place at the Yalova Training and Research Hospital within the Outpatient Chemotherapy Unit. The research will be conducted between May 1, 2026, and April 1, 2027.\n\nMethod and Participants:\n\nThe researchers plan to interview 10 to 20 participants who are over 18 years old and receiving treatment at the clinic. The final number of participants will be decided when the researchers find that no new information or themes are being discovered in the interviews (a stage called \"data saturation\").\n\nParticipants will:\n\nTake part in a private, one-on-one interview with a researcher.\n\nAnswer open-ended questions about their thoughts and feelings regarding their nursing care.\n\nAllow the interview to be voice-recorded to ensure all information is captured accurately.\n\nSpend approximately 30 to 45 minutes sharing their personal experiences.\n\nPrivacy and Ethics:\n\nParticipant privacy is a top priority. All personal information and voice recordings will be kept strictly confidential. In the final report, fake names (aliases) will be used so that no one can be identified. Participants can choose to leave the study at any time. The study follows international ethical rules to protect the rights of every participant.",[249,250,251],"Cancer Patients","Care","Chemotherapy",[253,254,255,256],"Individualized Care","Outpatient Chemotherapy","Patient Perception","Nursing Care","2026-04-20",{"date":231,"type":40},{"date":235,"type":21},{"date":261,"type":21},"2027-04-01",{"name":46,"class":47},{"id":264,"slug":265,"hasResults":11,"nctId":266,"briefTitle":267,"officialTitle":268,"acronym":4,"eligibilityCriteria":269,"healthyVolunteers":16,"sex":56,"minAge":18,"maxAge":270,"enrollmentInfo":271,"targetDuration":4,"studyType":22,"phases":273,"briefSummary":274,"conditions":275,"keywords":277,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":281,"lastUpdatePostDateStruct":282,"startDateStruct":284,"completionDateStruct":286,"leadSponsor":287,"locationsCount":48},"100630520","comparison-of-the-effects-of-different-chest-techniques-on-university-students-with-smoking-addiction-100630520","NCT07488741","Comparison of the Effects of Different Chest Techniques on University Students With Smoking Addiction","Comparison of the Effects of Chest PNF Techniques and Chest Mobility Exercises on Respiratory Function, Chest Expansion, and Functional Capacity in University Students With Smoking Addiction: A Single-Blind Randomized Controlled Study","Inclusion Criteria:\n\n* Age of 18-24 years\n* Fagerström Nicotine Dependence Questionnaire score ≥4\n* Smoking for at least 2 years\n* Daily smoking ≥5 cigarettes and at least 90 pack-years. Stable condition (no acute respiratory infection in the last 4 weeks).\n* FEV1 ≥80%\n* Voluntary participation in the study\n* No orthopedic or neurological problems that would prevent participation in exercise\n\nExclusion Criteria:\n\n* Cardiac event or lung surgery in the last 6 months\n* Respiratory problems such as COPD, asthma\n* Orthopedic and neurological problems\n* Termination of volunteering","24 Years",{"count":272,"type":21},30,[24],"Smoking is a significant risk factor for heart, lung, and respiratory system diseases, and is particularly prevalent among young people and university students. In Turkey, tobacco use is high in the 15-24 age group, and smoking rates among university students are reported to be between 20% and 43%. Besides causing COPD and other respiratory diseases, smoking negatively impacts performance by increasing fatigue, dyspnea, and pain during exercise. It impairs lung function, reducing respiratory volumes such as FVC and FEV1. PNF and chest mobility exercises targeting the chest area can improve respiratory parameters by increasing respiratory muscle function and thoracic mobility. Recent studies show that chest PNF techniques have positive effects on lung function, chest expansion, and some physiological parameters, especially in smokers.",[276],"Smoking",[278,279,280],"Smokers","Exercise","Proprioceptive Neuromuscular Facilitation (PNF) Stretching","2026-03-22",{"date":283,"type":40},"2026-03-25",{"date":285,"type":40},"2026-03-09",{"date":153,"type":21},{"name":46,"class":47},{"id":289,"slug":290,"hasResults":11,"nctId":291,"briefTitle":292,"officialTitle":293,"acronym":4,"eligibilityCriteria":294,"healthyVolunteers":11,"sex":56,"minAge":18,"maxAge":4,"enrollmentInfo":295,"targetDuration":4,"studyType":22,"phases":297,"briefSummary":298,"conditions":299,"keywords":301,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":304,"lastUpdatePostDateStruct":305,"startDateStruct":307,"completionDateStruct":308,"leadSponsor":309,"locationsCount":48},"100624209","different-inspiratory-muscle-trainings-in-patients-with-copd-100624209","NCT07406659","Different Inspiratory Muscle Trainings in Patients With COPD","Early Effects of Different Inspiratory Muscle Training on Disease Clinical Course, Respiratory Parameters, Functional Capacity and Quality of Life in Patients With COPD","Inclusion Criteria:\n\nHaving a COPD diagnosis according to GOLD criteria Having not had an acute exacerbation within the last month Being able to walk independently Having no communication problems Voluntarily participating in the study\n\nExclusion Criteria:\n\nBeing in a COPD exacerbation Having an orthopedic or neurological disease that would prevent assessment and treatment Having uncontrolled hypertension and heart disease",{"count":296,"type":21},51,[24],"COPD is one of the most life-threatening pulmonary diseases. According to the World Health Organization, it is expected to rise to the third leading cause of death by 2030. Smoking is the most significant contributing factor. COPD reduces lung volumes and causes dyspnea. Over time, respiratory muscle weakness develops, leading to hypercapnia, dyspnea, nocturnal oxygen desaturation, and decreased exercise performance. Pulmonary rehabilitation is the most important component of COPD treatment. Respiratory muscle training should be a mandatory component of the pulmonary rehabilitation program. Combining inspiratory muscle training with functional exercises allows the focus to be on respiratory muscle functions beyond the task of breathing. The purpose of this study was to investigate the effects of Functional Inspiratory Muscle Training on the course of the disease.",[300],"Chronic Obstructive Pulmonary Disease",[300,302,303],"Respiratory Muscle Training","Lung Capacities","2026-03-11",{"date":306,"type":40},"2026-03-16",{"date":304,"type":40},{"date":153,"type":21},{"name":46,"class":47},{"id":311,"slug":312,"hasResults":11,"nctId":313,"briefTitle":314,"officialTitle":315,"acronym":4,"eligibilityCriteria":316,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":317,"targetDuration":4,"studyType":22,"phases":319,"briefSummary":320,"conditions":321,"keywords":323,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":328,"lastUpdatePostDateStruct":329,"startDateStruct":331,"completionDateStruct":333,"leadSponsor":335,"locationsCount":4},"100597612","effect-of-different-foot-baths-on-postpartum-insomnia-and-fatigue-100597612","NCT07060755","Effect of Different Foot Baths on Postpartum Insomnia and Fatigue","Effect of Foot Bath With Peppermint Oil on Postpartum Insomnia and Fatigue Compared to Foot Bath With Warm Water Alone in the Postpartum Period","Inclusion Criteria:\n\n* Giving birth at term (38-42 weeks of gestation)\n* Being within the first 24 hours postpartum\n* Participating in the study voluntarily\n* Being over 18 years of age\n\nExclusion Criteria:\n\n* Having a risky pregnancy diagnosis\n* Having complications during and after birth\n* Having a cardiovascular system disease diagnosis\n* Having an open wound in the foot area\n* Having any skin problems in the foot area (such as fungus)\n* Having communication problems",{"count":318,"type":21},90,[24],"The goal of this clinical trial is to assess if different footbaths works to decrease postpartum fatigue and insomnia. The main questions are:\n\nDoes peppermint oil footbaths decrease fatigue and insomnia in postpartum period? Does peppermint oil footbaths more effective than footbaths with warm water?\n\nResearchers will compare peppermint oil footbath, warm water footbath to no intervention.\n\nParticipants will:\n\nAnswer some scales and questionnaire. Do peppermint oil footbath or warm water footbath for 30 minutes each day postpartum during 2 weeks.",[322],"Postpartum",[324,325,326,327],"fatigue","insomnia","sleepiness","footbath","2025-08-11",{"date":330,"type":40},"2025-08-15",{"date":332,"type":21},"2025-09-01",{"date":334,"type":21},"2026-09-30",{"name":46,"class":47},{"id":337,"slug":338,"hasResults":11,"nctId":339,"briefTitle":340,"officialTitle":341,"acronym":4,"eligibilityCriteria":342,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":343,"targetDuration":4,"studyType":22,"phases":344,"briefSummary":345,"conditions":346,"keywords":348,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":328,"lastUpdatePostDateStruct":352,"startDateStruct":353,"completionDateStruct":354,"leadSponsor":355,"locationsCount":4},"100597613","the-effect-of-mandala-coloring-on-perinatal-grief-and-psychological-resilience-levels-in-women-experiencing-perinatal-loss-100597613","NCT07060768","The Effect of Mandala Coloring on Perinatal Grief and Psychological Resilience Levels in Women Experiencing Perinatal Loss","The Effect of Mandala Coloring on Perinatal Grief and Psychological Resilience Levels in Women Experiencing Perinatal Loss: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Experienced perinatal loss (neonatal death, fetal death, abortion) within the last six weeks\n\nExclusion Criteria:\n\n* Serious psychological problem that requires intervention with the recommendation of a psychiatrist, such as having a previous mental disorder or use of antidepressants.\n* Practicing alternative methods such as yoga, meditation, acupuncture",{"count":218,"type":21},[24],"The goal of this clinical trial is to evaluate if mandala colouring helps to decrease grief symptoms and increase resilience in women who experienced perinatal loss.\n\nThe main questions are:\n\nDoes mandala coloring decrease perinatal grief symptoms? Does mandala coloring increase resilience?\n\nResearchers will compare mandala coloring intervention with standard perinatal loss nursing care to evaluate if mandala coloring works to decrease grief symptoms.\n\nParticipants will:\n\nAnswer some questionnaires and scales, and do mandala coloring at least for 20 minutes for 10 days after perinatal loss experience.",[347],"Perinatal Loss",[349,350,351],"perinatal loss","resilience","perinatal grief",{"date":330,"type":40},{"date":332,"type":21},{"date":334,"type":21},{"name":46,"class":47},{"id":357,"slug":358,"hasResults":11,"nctId":359,"briefTitle":360,"officialTitle":361,"acronym":4,"eligibilityCriteria":362,"healthyVolunteers":16,"sex":56,"minAge":18,"maxAge":363,"enrollmentInfo":364,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":366,"conditions":367,"keywords":369,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":371,"lastUpdatePostDateStruct":372,"startDateStruct":374,"completionDateStruct":376,"leadSponsor":378,"locationsCount":4},"100588442","effect-of-smartphone-usage-100588442","NCT06941454","Effect of Smartphone Usage","Investigating the Effect of Smartphone Usage on Balance and Dual Task Performance in University Students","Inclusion Criteria:\n\n* Between the ages of 18-30\n* Have a smartphone usage period of the last 7 days\n\nExclusion Criteria:\n\n* Having a severe medical condition\n* Having any disease that may affect cognitive level\n* Having any disease that may affect balance\n* Being pregnant\n* Having an orthopedic or neurological surgery within the last year\n* Using a mobility assistive device\n* Not owning a smartphone","30 Years",{"count":365,"type":21},50,"Screen time is defined as the time spent on many electronic and technological devices such as laptops, tablets, televisions, game consoles, and smartphones. The largest portion of screen time is made up of smartphones, which are currently used at very high rates. The increase in screen time, which describes the time an individual spends in front of technological devices, can pave the way for various physical problems when not controlled. The most important of these problems caused by excessive screen use due to increased smartphone use is postural disorders. Based on this, the original value of this research is to examine and reveal the effects of smartphone use on balance and dual-task performance. Scientific data can be reached on the negative effects of increased screen use caused by smartphone use.",[368],"Healthy Volunteers",[370],"smartphone","2025-04-15",{"date":373,"type":40},"2025-04-23",{"date":375,"type":21},"2025-05-15",{"date":377,"type":21},"2026-02-15",{"name":46,"class":47},""]