[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Mustafa Kemal University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":319},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,53,88,116,143,173,207,232,264,290],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100596464","body-awareness-therapy-in-high-stressed-young-adults-effects-on-function-balance-sleep-and-mood-100596464",false,"NCT07045792","Body Awareness Therapy in High Stressed Young Adults: Effects on Function, Balance, Sleep and Mood","Investigating the Effects of Body Awareness Therapy on Functional Capacity, Balance, Sleep Quality and Psychological State in Young Adults With High Stress Levels: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Be between 20 and 30 years old\n* Be literate\n* Score 10 or above on the stress subscale of the Depression Anxiety Stress Scale -21\n* Be willing to participate in the study voluntarily\n\nExclusion Criteria:\n\n* Individuals with orthopedic, neurological, rheumatological, psychiatric, mental, or any systemic chronic diseases\n* Those with cardiac problems that may prevent exercise\n* Those suspected of being pregnant\n* Individuals with malignancy\n* Individuals with active infection\n* Those who do not regularly attend the treatment program",true,"ALL","20 Years","30 Years",{"count":21,"type":22},30,"ESTIMATED","INTERVENTIONAL",[25],"NA","Body Awareness Therapy (BAT) is a holistic approach to human movement that considers the physical, physiological, psychological, and existential aspects of human existence. This planned randomized controlled study will be conducted on young adults with high stress levels. One group will be subjected to BAT and the other group will be the control group. The BAT exercises will be performed in supine, sitting and standing positions. In the BAT group, the exercises will be performed as a group exercise, not individually. After the initial evaluations in both the BAT and control groups, a re-evaluation will be performed at the end of 8 weeks. Functional capacity will be assessed with the 6-minute walk test, static balance with the single-leg balance test (eyes open-eyes closed), dynamic balance with the Y-balance test, psychological status with the Depression-Anxiety-Stress Scale-21 (DASS-21), and sleep quality with the Pittsburgh Sleep Quality Scale. BAT will be performed 2 days per week for 8 weeks and will be continued progressively. This study will examine the effects of BaT on functional capacity, balance, sleep quality, and psychological state in young adults with high stress levels.",[28,29,30,31],"Stress","Psychological Factors","Sleep","Postural Balance",[33,34,35,36,37,38,39,31],"Body Awareness Therapy","Stress Levels","Psychological Stress","Balance","Sleep Quality","Functional Capacity","Physical Therapy","RECRUITING","2026-06-29",{"date":43,"type":44},"2026-07-01","ACTUAL",{"date":46,"type":44},"2025-05-30",{"date":48,"type":22},"2026-06-28",{"name":50,"class":51},"Mustafa Kemal University","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":16,"sex":17,"minAge":60,"maxAge":61,"enrollmentInfo":62,"targetDuration":4,"studyType":23,"phases":64,"briefSummary":65,"conditions":66,"keywords":70,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":52},"100621819","outcomes-of-pulpotomy-and-root-canal-treatment-in-teeth-with-symptomatic-irreversible-pulpitis-100621819","NCT07375576","Outcomes of Pulpotomy and Root Canal Treatment in Teeth With Symptomatic Irreversible Pulpitis","Evaluation of the Outcomes of Total Pulpotomy, Radicular Pulpotomy, and Root Canal Treatment in Teeth With Extremely Deep Caries and Symptomatic Irreversible Pulpitis","Inclusion Criteria:\n\n* Healthy patients of both sexes, aged between 15 and 45 years, with no systemic diseases, will be screened for inclusion in the study. Strict eligibility criteria will be applied.\n\nThe patients included in the study must have restorable, extremely deep carious lesions in the mandibular first and second molars, and first and second premolars; healthy periodontal status (periodontal pocket ≤ 3 mm); and a clinical diagnosis of symptomatic irreversible pulpitis (history of spontaneous pain, pain persisting after removal of the stimulus, exaggerated and prolonged response to cold testing, and a positive response to the electric pulp test).\n\nExclusion Criteria:\n\n* Teeth with cracks or cusp fractures, subgingival caries, or periapical radiolucency will not be included in the study.\n\nInformed consent will be obtained from all included patients.","18 Years","45 Years",{"count":63,"type":22},99,[25],"The aim of this study is to evaluate the clinical effectiveness of total pulpotomy (TP), radicular pulpotomy (RP), and root canal treatment (RCT) in mandibular premolar and\u002For molar teeth diagnosed with symptomatic irreversible pulpitis, with respect to postoperative pain control and treatment success.Materials and Methods:A total of 99 mandibular premolar and molar teeth will be included in this study. The teeth will be randomly allocated into three groups (n = 33 per group): total pulpotomy, radicular pulpotomy, and root canal treatment.Root canal treatment will be performed using standardized endodontic protocols.Total pulpotomy will be carried out to the level of the canal orifices, followed by hemostasis achieved with 2.5% sodium hypochlorite (NaOCl). A 3-mm-thick layer of mineral trioxide aggregate (MTA) will be placed as the pulpotomy material.Radicular pulpotomy will be performed by removing the pulp tissue a few millimeters apical to the canal orifices. Hemostasis will be achieved using 2.5% NaOCl, and a 3-mm-thick layer of MTA will be placed as the pulpotomy agent.All treated teeth will be restored with glass ionomer cement, followed by a composite resin restoration.Postoperative pain intensity will be assessed using a visual analog scale (VAS) at the following time points: preoperatively, and at 12 hours, 24 hours, 48 hours, and 7 days postoperatively. Clinical and radiographic evaluations will be performed at 3, 6, and 12 months to assess treatment success and periapical health.",[67,68,69],"Post-operative Pain","Pulpitis - Irreversible","Success Rate",[71,72,73,74,75,76,77,78,79],"irreversibl pulpitis","total pulpotomy","radicular pulpotomy","vital pulp therapy (VPT)","root canal treatment (RCT)","pain assessment","vas scale","clinical follow - up","radiographic evaluation","2026-06-04",{"date":82,"type":44},"2026-06-05",{"date":84,"type":44},"2025-12-01",{"date":86,"type":22},"2027-08-01",{"name":50,"class":51},{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":4,"eligibilityCriteria":94,"healthyVolunteers":16,"sex":17,"minAge":60,"maxAge":95,"enrollmentInfo":96,"targetDuration":4,"studyType":23,"phases":98,"briefSummary":99,"conditions":100,"keywords":103,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":52},"100611210","the-effect-of-different-intracanal-medicaments-on-periapical-lesion-healing-100611210","NCT07237620","The Effect of Different Intracanal Medicaments on Periapical Lesion Healing","Comparison of Calcium Hydroxide and Diclofenac Sodium as Intracanal Medicaments on Periapical Healing: A Fractal Analysis Study","Inclusion Criteria:\n\nThe study is planned to include patients aged 18-60 years who are systemically healthy (ASA I-II), present with apical periodontitis after primary root canal treatment, and have single-rooted, root-filled mandibular teeth with a periapical index (PAI) score of ≥3.\n\nEndodontic treatment failure is to be evaluated based on clinical and radiographic examinations. The duration of the initial endodontic treatment is to be at least four years or longer and\u002For the teeth are to exhibit clinical symptoms and signs. Previous root canal fillings are to be assessed for obturation quality and classified as satisfactory if they meet the following criteria: no visible voids, good condensation, and termination within 1-2 mm of the radiographic apex. If one or more of these criteria are not fulfilled, the obturation is to be classified as poor quality.\n\nThe presence of post-treatment apical periodontitis, poor obturation quality, and\u002For persistent or newly developed symptoms (such as spontaneous pain, tenderness to palpation or percussion) and\u002For sinus tract formation are to be considered as indications for retreatment.\n\nExclusion Criteria:\n\nPatients with a history of psychiatric disorders, allergic reactions, or pregnancy, and those who have taken analgesics within seven days prior to treatment or antibiotics within the previous three months, are to be excluded from the study.\n\nTeeth presenting with a periodontal pocket depth greater than 4 mm, severe coronal destruction preventing rubber dam placement, vertical root fracture, internal or external resorption, ankylosis, overfilling, open apex, or that have undergone surgical or nonsurgical retreatment after primary therapy are to be excluded. Teeth with perforation or fractured instruments are also to be excluded.","60 Years",{"count":97,"type":22},60,[25],"This study is planned to evaluate the effects of two different intracanal medicaments-calcium hydroxide and diclofenac sodium-on periapical healing following endodontic retreatment. Fifty-four patients will be included and randomly assigned into two groups according to the type of medicament used. All procedures will be performed by a single experienced endodontist under standardized clinical conditions. Periapical lesion healing will be assessed radiographically at baseline and after 12 months using fractal analysis to quantitatively evaluate bone regeneration. The primary outcome will be the change in the fractal dimension values between the initial and follow-up radiographs.",[101,102],"Periapical Lesion Healing","Apical Periodontitis",[102,104,105,106,107,108],"intracanal medicaments","Diclofenac sodium","Calcium hydroxide","Fractal analysis","Endodontic retreatment",{"date":110,"type":44},"2026-06-08",{"date":112,"type":44},"2025-09-15",{"date":114,"type":22},"2027-04-01",{"name":50,"class":51},{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":123,"enrollmentInfo":124,"targetDuration":4,"studyType":23,"phases":126,"briefSummary":127,"conditions":128,"keywords":130,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":52},"100618212","basic-body-awareness-therapy-in-individuals-with-migraine-100618212","NCT07328685","Basic Body Awareness Therapy in Individuals With Migraine","Examining the Effectiveness of Basic Body Awareness Therapy in Individuals With Migraine","Inclusion Criteria:\n\n* Diagnosed with migraine,\n* Experiencing at least 3 migraine attacks per month,\n* Between the ages of 18 and 55 and who volunteer to participate in the study.\n\nExclusion Criteria:\n\n* History of secondary headaches,\n* Being pregnant,\n* Having any other neurological disease besides migraine,\n* Having other secondary headaches in addition to migraine,\n* History of malignancy,\n* Regularly practicing meditation, yoga, or mindfulness-based practices.","55 Years",{"count":125,"type":22},40,[25],"One biopsychosocial approach proven effective in headache treatment is basic body awareness therapy. This study was planned to evaluate the effectiveness of basic body awareness training and lifestyle recommendations in individuals diagnosed with migraine. Functional status will be assessed using the Migraine-Related Disability Assessment Scale (MIDAS), sleep quality using the Jenkins Sleep Scale (JUS), and quality of life using the Headache Impact Test. Assessment of functional status, sleep quality, and quality of life will be performed before treatment and after treatment (at the end of week 8).",[129],"Migraine",[131,132,133,134],"migraine","functional status","sleep","quality of life","2026-05-20",{"date":137,"type":44},"2026-05-22",{"date":139,"type":44},"2026-01-02",{"date":141,"type":22},"2026-08-01",{"name":50,"class":51},{"id":144,"slug":145,"hasResults":11,"nctId":146,"briefTitle":147,"officialTitle":148,"acronym":149,"eligibilityCriteria":150,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":151,"enrollmentInfo":152,"targetDuration":154,"studyType":155,"phases":4,"briefSummary":156,"conditions":157,"keywords":159,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":52},"100635572","ios-parameters-and-pap-titration-pressure-in-obstructive-sleep-apnea-100635572","NCT07554430","IOS Parameters and PAP Titration Pressure in Obstructive Sleep Apnea","Impulse Oscillometry for Prediction of PAP Titration Pressure in Obstructive Sleep Apnea (IOS-PAP Study)","IOS-PAP","Inclusion Criteria:\n\n* Adults aged 18 to 80 years\n* Diagnosed with obstructive sleep apnea (OSA) by overnight polysomnography (PSG)\n* Apnea-hypopnea index (AHI) ≥ 15\n* Undergoing positive airway pressure (PAP) titration (CPAP or BPAP)\n* Able to perform impulse oscillometry (IOS) test\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Central sleep apnea\n* Neuromuscular disease or restrictive lung disease\n* Recent upper airway infection (\\\u003C 2 weeks)\n* Incomplete PSG or IOS data\n* Inability to cooperate with testing procedures","80 Years",{"count":153,"type":22},92,"4 Weeks","OBSERVATIONAL","This prospective observational study aims to investigate whether impulse oscillometry (IOS)-a non-invasive lung function test-can help predict the specific pressure settings needed for positive airway pressure (PAP) therapy in patients with obstructive sleep apnea (OSA).\n\nCurrently, finding the optimal therapeutic pressure for OSA patients typically requires a titration process during sleep. This study explores if IOS parameters, which measure airway resistance and elasticity through small pressure oscillations during normal breathing, correlate with the final titration pressures (CPAP, EPAP, IPAP, and ΔP) determined by polysomnography.\n\nAdult patients diagnosed with moderate-to-severe OSA (Apnea-Hypopnea Index ≥ 15) will undergo standard diagnostic sleep testing followed by IOS testing using the Vyaire Vyntus BodyBox® system. The researchers will evaluate whether these respiratory measurements can accurately predict required airway pressures and if they can help clinicians distinguish between patients who need Continuous Positive Airway Pressure (CPAP) versus Bilevel Positive Airway Pressure (BPAP) therapy.",[158],"Obstructive Sleep Apnea (OSA)",[160,161,162,163],"obstructive sleep apnea","positive airway pressure","cpap","bpap","NOT_YET_RECRUITING","2026-04-21",{"date":167,"type":44},"2026-04-28",{"date":169,"type":22},"2026-05-01",{"date":171,"type":22},"2027-01-02",{"name":50,"class":51},{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":178,"acronym":4,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":4,"enrollmentInfo":180,"targetDuration":4,"studyType":23,"phases":182,"briefSummary":183,"conditions":184,"keywords":188,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":202,"completionDateStruct":204,"leadSponsor":206,"locationsCount":52},"100616578","effect-of-narrative-education-on-glycemic-control-in-adults-with-type-2-diabetes-in-primary-care-100616578","NCT07307430","Effect of Narrative Education on Glycemic Control in Adults With Type 2 Diabetes in Primary Care","Effect of a Structured Narrative Education Program on Glycemic Control in Adults With Type 2 Diabetes in Primary Care: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Diagnosis of type 2 diabetes mellitus for at least 1 year\n* HbA1c ≥ 7.0% measured within the last 3 months prior to enrollment\n* Followed in the study family health center and reachable by telephone\n* Able to read and write (or able to complete questionnaires with investigator assistance)\n* Provides written informed consent\n\nExclusion Criteria:\n\n* Type 1 diabetes, gestational diabetes, or secondary diabetes\n* Acute infection or hospitalization within the last 2 weeks\n* Major surgery or blood transfusion within the last 3 months\n* Active malignancy or current systemic steroid\u002Fimmunosuppressive therapy\n* Significant cognitive impairment preventing participation\n* Current participation in another structured diabetes education program",{"count":181,"type":22},226,[25],"Type 2 diabetes is common in primary care, and daily self-care behaviors are essential for achieving blood sugar targets. This randomized, two-arm clinical trial will evaluate whether a structured narrative education program added to usual diabetes care improves glycemic control compared with usual care alone in adults with type 2 diabetes. Eligible participants (age ≥18 years) with suboptimal glycemic control (HbA1c ≥7.0% in the last 3 months) will be randomized 1:1 to either standard care or standard care plus narrative education. The narrative education program will be delivered by a family physician over 3 months and includes two individual face-to-face sessions (approximately 20-30 minutes) at Day 0 and Day 15 and four brief telephone reinforcement calls (approximately 3-5 minutes) on Days 30, 45, 60, and 75.\n\nThe primary outcome is the absolute change in HbA1c from baseline (Day 0) to Day 90. Secondary outcomes include changes in diabetes self-care activities (SDSCA-TR), diabetes-related distress (PAID-5-TR), and body mass index (BMI) from Day 0 to Day 90.",[185,186,187],"Type 2 Diabetes Mellitus (T2DM)","Diabetes Self-management","Diabetes Education",[189,190,191,192,193,194,195,196,197,198],"Primary care","Narrative education","Diabetes self-management","HbA1c","Randomized controlled trial","Self-care behaviors","SDSCA","PAID-5","Family medicine","Behavioral intervention","2025-12-26",{"date":201,"type":44},"2025-12-31",{"date":203,"type":22},"2026-02-15",{"date":205,"type":22},"2026-11-15",{"name":50,"class":51},{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":211,"acronym":4,"eligibilityCriteria":212,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":213,"enrollmentInfo":214,"targetDuration":4,"studyType":23,"phases":216,"briefSummary":217,"conditions":218,"keywords":220,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":224,"lastUpdatePostDateStruct":225,"startDateStruct":227,"completionDateStruct":229,"leadSponsor":231,"locationsCount":52},"100602793","evaluation-of-the-effects-of-the-low-level-laser-therapy-as-an-adjunct-to-nonsurgical-treatment-in-patients-with-periimplantitis-100602793","NCT07128134","Evaluation of the Effects of the Low-level Laser Therapy as an Adjunct to Nonsurgical Treatment in Patients With Periimplantitis","Inclusion Criteria:\n\n* The patient must be willing to participate in the study.\n* At least one implant with a pocket depth ≥ 6 mm and radiographic bone loss ≥ 3 mm diagnosed with peri-implantitis.\n* Individuals aged 18-65.\n* Patients who can understand and maintain oral hygiene education.\n\nExclusion Criteria:\n\n* Individuals with any systemic disease that affects periodontal healing (diabetes, cancer, HIV\u002FAIDS, acute infections, liver or kidney dysfunction\u002Finsufficiency, autoimmune disorders: rheumatoid arthritis, systemic lupus erythematosus, Hashimoto's thyroiditis)\n* Female patients who are pregnant or breastfeeding\n* Patients who have undergone periodontal treatment within the last six months\n* Patients who have used antibiotics and regular anti-inflammatory medications within the last six months\n* Use of medications that affect periodontal tissues (cyclosporine, phenytoin, sodium valproate, etc.).","65 Years",{"count":215,"type":22},72,[25],"The main objective of this study is to evaluate the clinical efficacy of low-level laser therapy (LLLT) in addition to non-surgical periodontal treatment in patients with peri-implantitis. The study aims to investigate the anti-inflammatory and regenerative effects of low-level laser therapy on peri-implant soft and hard tissues and to reveal its contribution to treatment success.\n\nIn this context, the specific objectives of the study are as follows:\n\n1. To evaluate the effects of LLLT added to non-surgical mechanical treatment on clinical parameters such as plaque index, probing depth, bleeding index, and clinical attachment level.\n2. To examine the contributions of laser therapy to tissue healing by analyzing biochemical markers in peri-implant sulcular fluid over time.",[219],"Periimplantitis",[221,222,223],"Peri-implantitis","Laser therapy","Non-surgical treatment","2025-08-15",{"date":226,"type":44},"2025-08-17",{"date":228,"type":22},"2025-08-20",{"date":230,"type":22},"2026-06-30",{"name":50,"class":51},{"id":233,"slug":234,"hasResults":11,"nctId":235,"briefTitle":236,"officialTitle":237,"acronym":4,"eligibilityCriteria":238,"healthyVolunteers":16,"sex":17,"minAge":60,"maxAge":4,"enrollmentInfo":239,"targetDuration":4,"studyType":155,"phases":4,"briefSummary":240,"conditions":241,"keywords":248,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":257,"startDateStruct":259,"completionDateStruct":261,"leadSponsor":262,"locationsCount":263},"100579141","comparison-of-the-effectiveness-of-high-fidelity-simulation-and-low-fidelity-simulation-in-active-external-bleeding-control-management-of-caregivers-of-elderly-individuals-100579141","NCT06820437","Comparison of the Effectiveness of High Fidelity Simulation and Low Fidelity Simulation in Active External Bleeding Control Management of Caregivers of Elderly Individuals","Comparison of the Effectiveness of High-Fidelity Simulation and Low-Fidelity Simulation in the Management of Active External Bleeding Control by Caregivers of Elderly Individuals","Inclusion Criteria:\n\n* Not having received the theoretical first assessment and first aid training in external bleeding\n* No cognitive and communication problems that can actively participate in the study\n* Not being a health professional\n* Not being a paid caregiver\n\nExclusion Criteria:\n\n* The participant declares that he\u002Fshe wants to leave at any stage of the study\n* Not participating in any of the simulation phases\n* Not participating in the implementation of the data collection tools to be applied",{"count":21,"type":22},"The elderly population is increasing worldwide. Due to the increase in the elderly population, emergencies related to ageing are also encountered more frequently. One of these emergencies is trauma in the elderly. Traumas are frequently seen in elderly individuals due to physiological deficiencies related to aging as well as environmental factors. External bleeding caused by trauma is also encountered. If first aid to stop active external bleeding is not administered in a timely and correct manner, death due to bleeding can occur. Nowadays, elderly individuals live either with their families, alone, or in institutions. In the event of external bleeding, either the individual themselves, caregiving family members, or staff at the institution should be able to perform first aid to stop the bleeding.\n\nElderly individuals may not be able to perform first aid due to cognitive and neurological deficiencies. The ability of caregivers to provide first aid can be life-saving. If caregivers of elderly individuals are trained in first aid for external bleeding, they can quickly and correctly administer first aid to stop the bleeding. First aid training often consists of didactic education and demonstrations. A training strategy that ensures knowledge retention and skill acquisition is simulation training. This study aims to evaluate and compare the effectiveness of high-fidelity simulation and low-fidelity (Visually Enhanced Mental Simulation - VEMS) simulation in the skills of caregivers for elderly individuals in managing active external bleeding control.\n\nThe population of the study will consist of non-health professional caregivers of elderly individuals living in Antakya district of Hatay province. The sample size, calculated using the G Power program, has been determined to include 30 caregivers of elderly individuals. The study consists of four main work packages. In the first stage, the simulation environment will be prepared, and in the second stage, a preliminary application of the project will be conducted. In the third stage, the implementation of the research and the completion of checklists will be ensured. For this, volunteer caregivers of elderly individuals will be identified. After theoretical training is given to the participants, they will be assigned to intervention group 1 (VEMS) and intervention group 2 (high-fidelity simulation) using simple randomization. Following a pre-assessment with low-fidelity simulation, participants will undergo simulation training according to their intervention groups. Subsequently, a final assessment will be conducted using the same lowfidelity simulation. In the final stage, data analysis and interpretation of the findings will be carried out. The collected data will be analyzed statistically, and the significance level will be accepted as p\\\u003C0.05. With this study, insight will be provided into the effectiveness of VEMS and high-fidelity simulation in first aid training for active external bleeding for caregivers of elderly individuals. On the other hand, it is planned that the project results will be published in at least one article in journals indexed in the SSCI Expanded.",[242,243,244,245,246,247],"Simulation Training","High Fidelity Simulation Training","First Aid","Informal Caregivers","Elderly","Bleeding",[249,250,251,252,253,254,255],"Elderly caregivers","external bleeding","elderly","first aid training","simulation","visually enhanced mental simulation","high fidelity simulation","2025-02-05",{"date":258,"type":44},"2025-02-11",{"date":260,"type":22},"2025-02-20",{"date":228,"type":22},{"name":50,"class":51},2,{"id":265,"slug":266,"hasResults":11,"nctId":267,"briefTitle":268,"officialTitle":269,"acronym":4,"eligibilityCriteria":270,"healthyVolunteers":16,"sex":17,"minAge":60,"maxAge":4,"enrollmentInfo":271,"targetDuration":4,"studyType":23,"phases":273,"briefSummary":274,"conditions":275,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":282,"lastUpdatePostDateStruct":283,"startDateStruct":285,"completionDateStruct":287,"leadSponsor":289,"locationsCount":52},"100548046","effect-of-4-7-8-breathng-technque-on-shoulder-pan-and-respratory-functon-tests-after-laparoscopc-cholesectectomy-100548046","NCT06415890","Effect of 4-7-8 Breathıng Technıque on Shoulder Paın and Respıratory Functıon Tests After Laparoscopıc Cholesectectomy","The Effect of Usıng The 4-7-8 Breathıng Technıque on Postoperatıve Shoulder Paın and Respıratory Functıon Tests After Laparoscopıc Cholecystectomy","Inclusion Criteria:\n\n* Undergoing elective laparoscopic cholecystectomy,\n* Admitted to the clinic at least 2 hours before the surgical procedure,\n* Open to communication and cooperation,\n* Written and verbal permission to participate in the study was obtained,\n* Conscious, oriented and cooperative,\n* No cognitive and mental problems,\n* Speaks and understands Turkish,\n* American Society of Anesthesiologists (ASA) classification scores of I and II,\n* Hospitalized at least one night after surgical intervention,\n* Patients aged 18 years and older will be included in the study.\n\nExclusion Criteria:\n\n* Undergoing emergency laparoscopic cholecystectomy,\n* Open cholecystectomy,\n* Not admitted to the clinic at least 2 hours before the surgical procedure,\n* Not open to communication and cooperation,\n* Written and verbal permission to participate in the research could not be obtained,\n* Unconscious, disoriented and uncooperative,\n* Cognitively and mentally impaired,\n* Speaking Turkish but not understanding it,\n* Discharged on the same day after surgical intervention,\n* ASA score III and above,\n* Patients aged 18 years and younger will not be included in the study.",{"count":272,"type":22},98,[25],"This study was planned as a randomized controlled clinical trial to determine the effect of 4-7-8 breathing technique on shoulder pain and pulmonary function tests after laporoscopic cholecystectomy. A sample of 96 patients will be randomly assigned to the study and control groups. The study group will be administered the 4-7-8 breathing technique after LK, while the control group will be given routine care of the ward. Shoulder pain and pulmonary function tests will be measured in the first 24 hours and at discharge. The data obtained will be analyzed by appropriate statistical methods.",[276,277,278,279,280,281],"Laparoscopic Cholecystectomy","Breathing Exercise","Pulmonary Function Test","Shoulder Pain","Surgical Nursing","4-7-8 Breathing Technique","2024-09-07",{"date":284,"type":44},"2024-09-19",{"date":286,"type":44},"2024-08-25",{"date":288,"type":22},"2025-07-15",{"name":50,"class":51},{"id":291,"slug":292,"hasResults":11,"nctId":293,"briefTitle":294,"officialTitle":295,"acronym":4,"eligibilityCriteria":296,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":213,"enrollmentInfo":297,"targetDuration":4,"studyType":23,"phases":299,"briefSummary":300,"conditions":301,"keywords":305,"overallStatus":164,"whyStopped":4,"lastUpdateSubmitDate":311,"lastUpdatePostDateStruct":312,"startDateStruct":314,"completionDateStruct":316,"leadSponsor":318,"locationsCount":52},"100513759","comparison-of-the-effectiveness-heavy-slow-resistance-and-eccentric-training-in-rotator-cuff-tendinopathy-100513759","NCT05969652","Comparison of the Effectiveness Heavy Slow Resistance and Eccentric Training in Rotator Cuff Tendinopathy","Comparison of the Effectiveness of Supervised Heavy Slow Resistance Training and Eccentric Exercise Training in Patients With Rotator Cuff Tendinopathy: A Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n* Describing subacromial pain\n* Rotator cuff tendinopathy (subacromial impingement syndrome, biceps tendinitis and rotator cuff I. and II. stage diagnosis)\n* Continuation of diagnostic symptoms for at least 30 days\n\nExclusion Criteria:\n\n* Prior shoulder surgery\n* Sign of cervical radiculopathy\n* Shoulder instability or history of upper extremity fracture\n* Full-thickness rotator cuff tear\n* Adhesive capsulitis\n* Humeroscapular periarthritis (osteoarthritis, inflammatory arthropathies, etc.)\n* Neoplasm\u002Fmalignant status\n* Other independent from shoulder problem being on regular analgesic therapy for ongoing painful conditions\n* Subacromial corticosteroids in the last 2 months having received an injection or participating in a shoulder rehabilitation program",{"count":298,"type":22},20,[25],"Rotator cuff tendinopathy, also called subbracromial impingement syndrome, is one of the most important causes of anterior shoulder pain. Although exercise training is known as an effective intervention method in the treatment of rotator cuff\u002Fsubacromial impingement problems, there is no definite consensus on which type of exercise is more effective. The aim of this study is to analyze and compare the effects of the Heavy Slow Resistance (HSR) training and eccentric exercise training on pain, function, supraspinatus tendon structure, muscle strength, range of motion, subjective perception of improvement and treatment satisfaction in individuals with subacromial shoulder pain associated with rotator cuff tendinopathy.",[302,303,304],"Rotator Cuff Tendinopathy","Subacromial Impingement Syndrome","Bicep Tendinitis",[306,307,308,309,310],"Exercise therapy","Rehabilitation","Resistance training","Shoulder pain","Subacromial impingement syndrome","2024-06-26",{"date":313,"type":44},"2024-06-27",{"date":315,"type":22},"2026-01-31",{"date":317,"type":22},"2026-12-31",{"name":50,"class":51},""]