[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Muğla Sıtkı Koçman University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":367},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,44,72,99,133,160,192,219,243,289,317,343],{"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":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100635281","early-rehabilitation-after-total-hip-arthroplasty-100635281",false,"NCT07550647","Early Rehabilitation After Total Hip Arthroplasty","Effect of Early Rehabilitation on Functional Recovery After Total Hip Arthroplasty: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients scheduled for unilateral total hip arthroplasty due to osteoarthritis or developmental dysplasia of the hip (DDH)\n* Aged between 50 and 75 years\n* Willing and able to participate in all follow-up assessments\n* Able to comply with assessment procedures\n* Able to meet the requirements of telerehabilitation\n* Undergoing surgery with a standardized surgical protocol\n\nExclusion Criteria:\n\n* Previous history of total hip arthroplasty on either side\n* Planned revision total hip arthroplasty\n* Severe osteoarthritis in the contralateral hip\n* Presence of severe acute metabolic, neuromuscular, or cardiovascular disease\n* History of active malignancy\n* Presence of respiratory infection\n* Concomitant orthopedic conditions (e.g., lower extremity fractures, severe hip\u002Fknee deformities, lumbar or sacroiliac dysfunction)\n* Body mass index \\>35\n* Occurrence of postoperative complications (e.g., prosthetic infection, thromboembolic events, or conditions requiring reoperation)","ALL","50 Years","75 Years",{"count":20,"type":21},52,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to investigate the effects of an early postoperative rehabilitation program combined with neuromuscular electrical stimulation (NMES) and telerehabilitation on functional recovery in patients undergoing total hip arthroplasty (THA).\n\nIn the early postoperative period, patients commonly experience muscle weakness, impaired gait, and functional limitations that may delay recovery. Early rehabilitation has been shown to improve functional outcomes, while NMES may enhance muscle activation, particularly in hip abductor muscles. Additionally, telerehabilitation may support continuity of care following discharge by enabling supervised home-based exercise.\n\nIn this prospective study, participants will be assigned to either an intervention group receiving early physiotherapy combined with NMES and telerehabilitation, or a control group receiving standard postoperative care. Functional outcomes, gait parameters, quality of life, and muscle-related changes will be evaluated at predefined time points.",[27],"Total Hip Arthroplasty (THA)",[29,30],"Rehabilitation","Total Hip Arthtoplasty","RECRUITING","2026-04-19",{"date":34,"type":35},"2026-04-24","ACTUAL",{"date":37,"type":21},"2026-04",{"date":39,"type":21},"2027-10",{"name":41,"class":42},"Muğla Sıtkı Koçman University","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":43},"100616678","pain-diary-use-after-laparoscopic-cholecystectomy-100616678","NCT07308730","Pain Diary Use After Laparoscopic Cholecystectomy","Randomized Controlled Trial on the Use of Pain Diary in Assessing Early Postoperative Pain Following Laparoscopic Cholecystectomy","PDP-LC","Inclusion Criteria:\n\n1. Admitted for elective laparoscopic cholecystectomy\n2. Scheduled for first-time laparoscopic cholecystectomy\n3. Aged 18 years or older\n4. Able to speak, read, and understand Turkish\n5. Literate\n6. Communicative and cooperative\n7. ASA score of 1, 2, or 3\n8. Expected to stay at least 24 hours in the hospital post-surgery\n9. Capable of understanding study instructions\n10. Willing to participate voluntarily\n\nExclusion Criteria:\n\n1. Prolonged stay in the recovery unit due to extended effects of general anesthesia\n2. Admission to intensive care unit postoperatively\n3. Having chronic pain and receiving treatment for it\n4. Being a cancer patient\n5. Having a writing disability\n6. Inability to communicate\n7. Having cognitive, affective, verbal, visual, or auditory impairments\n8. Diagnosed psychiatric disorders such as anxiety or depression and using related medications\n9. Choosing to withdraw from the study after giving consent","18 Years",{"count":54,"type":21},142,[24],"This randomized controlled study aims to evaluate the effectiveness of using a pain diary in the assessment of early postoperative pain in patients undergoing laparoscopic cholecystectomy. Patients will be randomly assigned to a pain diary group or a control group receiving routine pain assessment. Postoperative pain intensity will be measured at predefined time points using standardized pain assessment tools. The study seeks to improve patient participation in postoperative pain evaluation without introducing additional pharmacological interventions.",[58,59],"Cholelithiasis","Postoperative Pain",[59,61,62,63],"Daily Pain Assessment","Laparoscopic Cholecystectomy","Pain Diary","2025-12-31",{"date":66,"type":35},"2026-01-06",{"date":68,"type":35},"2025-11-15",{"date":70,"type":21},"2027-01-30",{"name":41,"class":42},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":80,"enrollmentInfo":81,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":84,"conditions":85,"keywords":89,"overallStatus":91,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":96,"leadSponsor":98,"locationsCount":4},"100617787","determining-the-effect-of-education-given-to-patients-undergoing-outpatient-anal-fistula-surgery-100617787","NCT07323160","Determining the Effect of Education Given to Patients Undergoing Outpatient Anal Fistula Surgery","Determining the Effect of Discharge Education Provided Using the Teaching-back Method on Readmission Rates and Patient Satisfaction in Patients Undergoing Same-day Anal Fistula Surgery","anal fistula","Inclusion Criteria:\n\n* Having a day surgery planned, Being admitted to the Proctology Unit for anal fistula surgery, Being undergoing elective anal fistula surgery for the first time, Being planned to have a surgical procedure performed with local anesthesia, Being over 18 years of age, Being able to read and understand Turkish, Being able to read and understand the research instructions, Being literate, Agreeing to participate in the research.\n\nExclusion Criteria:\n\n* Having surgery planned with general anesthesia, Requiring general anesthesia during the surgical procedure, Being hospitalized for more than 24 hours, Having a recurrent anal fistula, Having another anorectal disease besides the anal fistula, such as advanced Crohn's disease or colorectal cancer, Having complications within 24 hours of surgery and rescheduling surgery, Having visual, auditory, or cognitive problems, Having agreed to participate in the study but wishing to withdraw during follow-up.","90 Years",{"count":82,"type":21},76,[24],"It is emphasized that discharge education should shift from traditional healthcare provider-centered, one-way education to patient-centered education based on patient-care provider interaction to ensure patients' active participation in their own care, adherence to the recommended treatment plan, and maintenance of surgical success after outpatient anal fistula surgery. In this context, it is suggested that an effective education method such as teach-back can be used in clinical settings to teach patients complex health information and facilitate their understanding of discharge education. While studies exist in the literature evaluating the impact of health literacy after general surgery, no studies have been found specifically evaluating health literacy and discharge education for anal fistula surgery. Furthermore, it is emphasized that further research is needed to improve the quality of postoperative care after anal fistula surgery and to better understand the factors contributing to unplanned hospital returns. Based on this need, this study is a randomized controlled trial with a pretest and posttest approach aimed at determining the effect of teach-back-based discharge education on hospital readmission and patient satisfaction in outpatient anal fistula surgery patients. The study sample was calculated as a total of 68 people, 34 in each group, based on a power analysis performed with the GPower 3.1. 9.7 program, using a type 1 error of 0.05, a type 2 error of 0.20, and an effect size of 0.70 to determine the difference in measurements between the groups. Considering the possible attrition in the study, the sample size was increased by 10%, and a total of 76 people, 38 in each group, were planned to be included in the study. Following Ethics Committee approval and institutional permissions, the study data will be collected using the Individual Identification Form, Health Literacy Scale, Anal Fistula Surgery Discharge Education Knowledge Test, Discharge Satisfaction Scale, and Post-Discharge Follow-up Form, from patients scheduled for and undergoing outpatient anal fistula surgery at Muğla Training and Research Hospital between November 15, 2025, and January 30, 2027. The research will be conducted in three phases: the development of the education brochure and knowledge test, and the preoperative and postoperative phases. The \"Anal Fistula Surgery Discharge Education Knowledge Test\" was developed to assess patients' knowledge of anal fistula and its care. The \"Anal Fistula Surgery Discharge Education Patient Booklet\" was developed by the researchers using literature review and consultation with a General Surgery Specialist specializing in anal fistulas to provide specific training on anal fistula surgery and postoperative care. These were then sent to specialists for expert opinion. All patients presenting to the General Surgery Outpatient Clinic for anal fistula surgery who meet the inclusion criteria will be interviewed face-to-face before surgery to be informed about the study. Patients who agree to participate will be asked to sign a consent form. Because outpatient surgeries involve admission and discharge within 24 hours, and patients arrive at the Proctology Unit on the day of surgery, all patients will be summoned to the General Surgery Outpatient Clinic the day before surgery and will complete the \"Individual Identification Form,\" \"Health Literacy Scale,\" and \"Anal Fistula Surgery Discharge Education Knowledge Test.\" Patients will be assigned to the intervention (discharge education via teach-back) and control groups using a block randomization table based on their order of admission to the Proctology Unit for the surgical procedure. Patients in the intervention group will receive discharge education via teach-back using the \"Anal Fistula Surgery Discharge Education Patient Booklet.\" Education will continue until the patient accurately recounts the information to the principal investigator and is confident that the patient has understood the instruction correctly. The control group will receive standard patient education in the clinic and will not receive any intervention. Postoperatively, all patients in both groups will complete the \"Anal Fistula Surgery Discharge Education Knowledge Test\" post-test and the Discharge Education Satisfaction Scale before being discharged from the unit. Patients in both groups will be contacted weekly for 30 days to monitor their progress. Because the study will provide training, blinding of the assessments will not be possible.",[86,87,88],"Anal Fistula","Patient Discharge Education","Outpatient Anal Surgery",[90],"Anal fistula, Day surgery, Discharge teaching, Patient satisfaction, Readmission","NOT_YET_RECRUITING","2025-12-23",{"date":94,"type":35},"2026-01-07",{"date":64,"type":21},{"date":97,"type":21},"2027-05-15",{"name":41,"class":42},{"id":100,"slug":101,"hasResults":11,"nctId":102,"briefTitle":103,"officialTitle":104,"acronym":105,"eligibilityCriteria":106,"healthyVolunteers":11,"sex":16,"minAge":107,"maxAge":108,"enrollmentInfo":109,"targetDuration":4,"studyType":111,"phases":4,"briefSummary":112,"conditions":113,"keywords":118,"overallStatus":91,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":132},"100607084","comparison-of-the-silverman-andersen-score-and-the-downes-score-100607084","NCT07183956","Comparison of the Silverman-Andersen Score and the Downes Score","Comparison of the Silverman-Andersen Score and the Downes Score in Assessing the Severity of Respiratory Distress and Predicting Noninvasive Ventilation Failure in Neonates","CSASDS","Inclusion Criteria:\n\n* Preterm infants born at \\>28 weeks of gestation or term infants born at ≥37 weeks of gestation.\n* Development of respiratory distress within the first 6 hours after birth, defined as the presence of at least two of the following: Respiratory rate ≥60\u002Fmin, Subcostal\u002Fintercostal retractions, Grunting.\n* Persistence of respiratory distress for more than 6 hours.\n* Age within the first 12 hours of life.\n* Silverman-Andersen score ≥3.\n* Receiving NIPPV support.\n\nExclusion Criteria:\n\n* Major congenital malformations.\n* Airway or pulmonary anomalies.\n* Cardiovascular or respiratory instability due to sepsis.\n* Cyanotic congenital heart disease.\n* Severe intraventricular hemorrhage.\n* Contraindications for NIPPV therapy (e.g., congenital nasal anomalies, congenital diaphragmatic hernia, abdominal wall defects).\n* Requirement of intubation or chest compressions in the delivery room.\n* Requirement of intubation within the first hour of life.\n* Death within the first 24 hours of life.\n* Gestational age ≤28 weeks.\n* Diagnosis of air leak syndrome (pneumothorax) prior to initiation of NIPPV therapy.","2 Hours","12 Hours",{"count":110,"type":21},220,"OBSERVATIONAL","This study aimed to compare the Silverman-Andersen score and the Downes score in predicting noninvasive ventilation (NIPPV) failure in preterm and term infants who received NIPPV support due to postnatal respiratory distress, as well as to evaluate the agreement of these scoring systems with other methods used to assess the severity of respiratory distress.\n\nThe present study was designed as a prospective, multicenter, observational study conducted with neonates undergoing noninvasive ventilation.",[114,115,116,117],"Respiratory Distress Neonatal","Noninvasive Ventilation","Intubation","Scoring Systems",[119,120,121,122,123],"Silverman-Andersen score","Downes score","Newborn","Respiratory distress","Noninvasive ventilation","2025-09-13",{"date":126,"type":35},"2025-09-19",{"date":128,"type":21},"2025-09-15",{"date":130,"type":21},"2027-02-15",{"name":41,"class":42},4,{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":139,"eligibilityCriteria":140,"healthyVolunteers":141,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":142,"targetDuration":144,"studyType":111,"phases":4,"briefSummary":145,"conditions":146,"keywords":148,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":43},"100604693","screening-for-alpha-1-antitrypsin-deficiency-in-patients-with-airway-obstruction-100604693","NCT07152834","Screening for Alpha-1 Antitrypsin Deficiency in Patients With Airway Obstruction","Evaluation of the Relationship Between Dyspnoea and Functional Airway Obstruction in Alpha-1 Antitrypsin Deficiency: A Prospective, Case-Control, Analytical Study","AATD-SAO","Inclusion Criteria:\n\n* Achieve a post-bronchodilator FEV1\u002FFVC ratio of 70 or above in the respiratory function test.\n* Be able to speak and understand Turkish.\n* Have the mental and cognitive capacity to understand the questions asked.\n\nExclusion Criteria:\n\n* Renal dysfunction; acute inflammation; rheumatological, haematological, or liver diseases; COPD; asthma; bronchiectasis; and a history of malignancy.\n* Pregnant women and users of oral contraceptives.",true,{"count":143,"type":21},734,"1 Day","Brief Summary:\n\nThis study aims to find out if a genetic condition called Alpha-1 Antitrypsin Deficiency (AATD) is more common in people who have shortness of breath and signs of airway obstruction on their breathing tests.\n\nAlpha-1 antitrypsin (AAT) is a protein that protects the lungs from damage. AATD is an inherited condition where the body does not make enough of this protein, which can lead to lung diseases like emphysema, especially in smokers.\n\nInvestigators hypothesize that low AAT levels or related genetic mutations may be a contributing factor to airway obstruction in patients complaining of shortness of breath.\n\nTo test this, investigators will recruit patients from our outpatient clinic who are being evaluated for shortness of breath and are having a standard breathing test (spirometry). Investigators will measure their AAT levels and test for the most common genetic mutations that cause AATD using a small blood sample. Investigators will then compare the AAT levels and genetic results between different groups of patients, such as smokers and non-smokers with and without airway obstruction. Investigators will also see if the severity of a patient's shortness of breath is related to their AAT levels.\n\nThe goal is to improve the detection of AATD in this patient population, which could lead to better diagnoses and specific treatments for those who have this condition.",[147],"Alpha 1-antitrypsin Deficiency (AATD)",[149,150,151],"Alpha 1-Antitrypsin Deficiency","Airway Obstruction","PRISm","2025-09-03",{"date":154,"type":35},"2025-09-10",{"date":156,"type":35},"2025-08-06",{"date":158,"type":21},"2026-01-05",{"name":41,"class":42},{"id":161,"slug":162,"hasResults":11,"nctId":163,"briefTitle":164,"officialTitle":165,"acronym":4,"eligibilityCriteria":166,"healthyVolunteers":11,"sex":16,"minAge":167,"maxAge":168,"enrollmentInfo":169,"targetDuration":4,"studyType":22,"phases":171,"briefSummary":172,"conditions":173,"keywords":177,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":190,"locationsCount":191},"100591192","remote-ischemic-preconditioning-in-type-2-diabetic-patients-undergoing-cabg-100591192","NCT06977230","Remote Ischemic Preconditioning in Type 2 Diabetic Patients Undergoing CABG","The Effect of Remote Ischemic Preconditioning on Myocardial Protection in Patients With Type 2 Diabetes Mellitus Undergoing Coronary Artery Bypass Graft Surgery: A Randomized Controlled Double-Blind Study","Inclusion Criteria:\n\n* Diagnosed with type 2 diabetes mellitus and receiving medical treatment\n* Scheduled for isolated elective coronary artery bypass graft (CABG) surgery\n* American Society of Anesthesiologists (ASA) physical status class III or IV\n* Age between 40 and 85 years\n\nExclusion Criteria:\n\nEmergency CABG surgery Reoperation (revision surgery) Left ventricular ejection fraction (LVEF) \\\u003C 40% History of cardiac arrest or cardiogenic shock Pregnancy Clinically significant peripheral arterial disease affecting the upper limbs Hepatic dysfunction (bilirubin \\> 20 μmol\u002FL or INR \\> 2.0) Renal failure (eGFR \\\u003C 20 mL\u002Fmin\u002F1.73 m²) Ongoing treatment with glibenclamide or nicorandil (agents known to interfere with ischemic preconditioning mechanisms) Asthma","45 Years","85 Years",{"count":170,"type":21},60,[24],"This randomized, double-blind, prospective clinical trial aims to investigate the effect of remote ischemic preconditioning (RIPC) on myocardial protection in patients with type 2 diabetes mellitus undergoing elective coronary artery bypass graft (CABG) surgery. Perioperative myocardial injury remains a significant concern during CABG, particularly in high-risk patients such as those with diabetes. RIPC is a low-cost, non-invasive intervention that may reduce myocardial damage by enhancing ischemic tolerance through intermittent limb ischemia.\n\nSixty patients aged 40-85 years with type 2 diabetes scheduled for isolated CABG will be randomized to either receive RIPC or standard care. RIPC will be applied through five cycles of upper limb cuff inflation and deflation prior to sternotomy. High-sensitivity troponin T levels will be measured at 24, 48, and 72 hours postoperatively to assess myocardial injury. Secondary outcomes include acute kidney injury (KDIGO classification), maximum vasoactive-inotropic score (VIS) during the first 72 postoperative hours, ICU and hospital length of stay. This study will provide insight into the cardioprotective role of RIPC in diabetic patients undergoing cardiac surgery.",[174,175,176],"Diabetes Mellitus","Coronary Artery Bypass","Remote Ischaemic Conditioning",[178,179,175,180,181,182,183],"High sensitive Troponin T","Diabetes mellitus Type 2","Myocardial Ischemia","Remote Ischemic Conditioning","Acute Kidney Injury","Cardioprotection","2025-06-15",{"date":186,"type":35},"2025-06-18",{"date":188,"type":35},"2025-05-26",{"date":128,"type":21},{"name":41,"class":42},2,{"id":193,"slug":194,"hasResults":11,"nctId":195,"briefTitle":196,"officialTitle":197,"acronym":4,"eligibilityCriteria":198,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":199,"targetDuration":144,"studyType":111,"phases":4,"briefSummary":201,"conditions":202,"keywords":209,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":211,"lastUpdatePostDateStruct":212,"startDateStruct":214,"completionDateStruct":216,"leadSponsor":218,"locationsCount":43},"100583583","cough-and-hemorrhoids-100583583","NCT06878209","Cough and Hemorrhoids","Is Cough a Predisposing Factor for Hemorrhoids? A Prospective, Analytical Study","Inclusion Criteria:\n\n1. Being 18 years of age or older\n2. Speaking and understanding Turkish\n3. To be mentally and cognitively capable of understanding the questions asked\n4. To agree to participate in the research\n5. individuals diagnosed with hemorrhoidal disease\n\nExclusion Criteria:\n\n1. Those with existing proctologic disease other than hemorrhoidal disease and pelvic floor disease\n2. Patients with previous surgery for hemorrhoidal disease\n3. Patients with hemorrhoidal disease caused by portal hypertension\n4. Patients during pregnancy and diagnosed with postpartum hemorrhoidal disease\n5. those with benign prostatic hyperplasia or neurogenic bladder that may cause increased intra-abdominal pressure",{"count":200,"type":21},134,"The aim of the study is to investigate the relationship between hemorrhoids and cough by assessing the symptoms, duration, and severity of cough in patients who will present to the general surgery outpatient clinic of Muğla Education and Research Hospital (MERH) with symptoms such as bleeding, pain, itching, fecal leakage, prolapse, and mucus discharge. These patients will be diagnosed with hemorrhoidal disease through rectal examination to detect anal pathology and will be graded according to mucosal prolapse. Our study will aim to determine whether cough is a predisposing factor for hemorrhoids by evaluating the presence, duration, and frequency of cough symptoms in patients with hemorrhoids. The study will be designed as a cross-sectional, analytical, and descriptive study. Between March 2025 and June 2025, patients with newly diagnosed hemorrhoids who will present to the MEAH General Surgery Outpatient Clinic will undergo physical examinations and will be assessed for cough symptoms. Evaluations will include height and weight measurements, the Leicester Cough Questionnaire, the Cough Visual Analog Scale (VAS) questionnaire, duration of cough (categorized as acute if shorter than 4 weeks, or chronic if longer than 4 weeks), timing of cough (day, night, or all day), comorbidities (such as COPD, asthma, chronic bronchitis, interstitial lung disease, idiopathic pulmonary fibrosis, and others), and smoking history (active, former, or never smoked). The primary endpoint will be to compare the relationship between the severity of hemorrhoids and the duration and frequency of cough in patients with both conditions. The secondary endpoint will be to compare the grade of hemorrhoids with comorbid chest diseases in these patients. The tertiary endpoint will be to compare the degree of hemorrhoids with the smoking history of patients who have both hemorrhoids and cough.",[203,204,205,206,207,208],"Hemorrhoid","Cough","Cough Duration","Cough Frequency","Cough Severity","Hemorrhoids, Internal",[210],"cough, hemorrhoid","2025-05-08",{"date":213,"type":35},"2025-05-11",{"date":215,"type":35},"2025-03-14",{"date":217,"type":21},"2025-10-14",{"name":41,"class":42},{"id":220,"slug":221,"hasResults":11,"nctId":222,"briefTitle":223,"officialTitle":224,"acronym":4,"eligibilityCriteria":225,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":226,"enrollmentInfo":227,"targetDuration":4,"studyType":22,"phases":229,"briefSummary":230,"conditions":231,"keywords":233,"overallStatus":91,"whyStopped":4,"lastUpdateSubmitDate":236,"lastUpdatePostDateStruct":237,"startDateStruct":238,"completionDateStruct":240,"leadSponsor":242,"locationsCount":43},"100570219","psychoeducation-based-on-acceptance-and-commitment-therapy-100570219","NCT06704399","Psychoeducation Based on Acceptance and Commitment Therapy","Investigation of the Effect of Acceptance and Commitment Therapy-Based Psychoeducation on Rumination and Self-Compassion in Patients Diagnosed With Panic Disorder: Randomized Controlled Study","Inclusion Criteria:\n\n* Patients diagnosed with Panic Disorder followed in Muğla Training and\n* Research Hospital Psychiatry Polyclinics,\n* Those between the ages of 18-65 who agree to participate in the research,\n* Those who were in a euthymic mood during the interview, according to physician control,\n* Those who speak Turkish,\n* Those who are literate,\n* Those who have a computer and internet access for the program to be conducted online if deemed necessary during the research process,\n* Not having undergone such training within the last year is within the scope of the inclusion criteria.\n\nExclusion Criteria:\n\n* Having a diagnosis of a psychiatric disease in addition to panic disorder,\n* Having an attack period during the training period,\n* Individuals with cognitive (diagnosed by a physician) and physical disability (hearing, speaking, etc.) are included in the exclusion criteria from the study.","65 Years",{"count":228,"type":21},50,[24],"The aim of this study is to manage individual psychoeducation in acceptance and commitment therapy for problems with panic disorder and to evaluate the effect of this program on rumination and self-resilience.",[232],"Panic Disorder",[234,235],"rumination","self-compassion","2025-05-07",{"date":211,"type":35},{"date":239,"type":21},"2025-09-30",{"date":241,"type":21},"2027-06-30",{"name":41,"class":42},{"id":244,"slug":245,"hasResults":11,"nctId":246,"briefTitle":247,"officialTitle":248,"acronym":4,"eligibilityCriteria":249,"healthyVolunteers":11,"sex":16,"minAge":250,"maxAge":251,"enrollmentInfo":252,"targetDuration":4,"studyType":22,"phases":254,"briefSummary":255,"conditions":256,"keywords":268,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":282,"lastUpdatePostDateStruct":283,"startDateStruct":284,"completionDateStruct":286,"leadSponsor":288,"locationsCount":43},"100520408","the-effect-of-motor-image-training-on-balance-performance-in-geriatric-individuals-100520408","NCT06056180","The Effect of Motor Image Training on Balance Performance in Geriatric Individuals","Investigation of the Effects of Motor Imagery Training Given With Action Observation on Balance Performance in Geriatric Individuals","Inclusion Criteria:\n\n1. To be between 60-80 years old\n2. Having the ability to speak, read, understand and write Turkish\n3. To have the cognitive skills to understand and apply the trainings to be applied in the study (with ≥ 24 points from the Mini Mental State Test)\n4. Being able to do activities of daily living independently\n5. Being able to walk independently (without using a walking aid and at least 10 meters)\n6. Having a body mass index of \\\u003C35 kg\u002Fm2 (not being severely obese or morbidly obese)\n\nExclusion Criteria:\n\n1. Having visual, hearing and sensory impairment\n2. To have had a trauma, lesion or surgery that may affect balance and musculoskeletal system in the last 6 months\n3. Having a history of 2 ≥ falls in the last 6 months\n4. Having any chronic lower extremity pain\n5. Having an acute or chronic illness that may cause problems with balance and falling\n6. Being diagnosed with sensory, vestibular and cerebellar ataxia\n7. Being on any medication that may cause problems with balance, focus, attention and falling.\n8. Exercising regularly, which may affect performance results\n9. To stop participating in the study for any reason","60 Years","80 Years",{"count":253,"type":21},46,[24],"The goal of this study \\[type of study: clinical trial\\] is to was planned to investigate the effect of motor imagery training given to geriatric individuals with action observation on their balance performance and to compare these two methods.\n\nThe main questions it aims to answer are:\n\n1. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving static balance than virtual reality-based balance training given alone?\n2. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving dynamic balance than virtual reality-based balance training given alone?\n3. Is virtual reality-based balance training given together with motor imagery for six weeks in geriatric individuals more effective in increasing balance confidence than virtual reality-based balance training given alone?\n\n46 geriatric individuals will be randomized into 2 groups. Along with action observation, motor imagery training and virtual reality-based balance training will be given to the study group. On the other hand, only virtual reality-based balance training will be given to the control group. All assessments will be repeated before and after the trainings. The trainings will be applied 2 days a week for 6 weeks. Each training session; 25 minutes for the control group and 45 minutes for the study group.",[257,258,259,260,261,262,263,264,265,266,267],"Imagery (Psychotherapy)","Postural Control","Postural Balance","Virtual Reality Therapy","Surface Electromyography","Geriatric Assessment","Physical Therapy Techniques","Physical Therapy","Healthy Ageing","Healthy Aging","Falling",[269,270,271,272,273,274,275,276,277,278,279,280,281],"visual motor imagery","kinesthetic motor imagery","postural control","virtual reality therapy","interactive video games","balance platform with pressure sensor","surface electromyography","balance confidence","fall risk","mobility","cognitive processing speed","smartphone gyroscope sensor dataset","action observation","2025-05-05",{"date":211,"type":35},{"date":285,"type":35},"2023-11-01",{"date":287,"type":21},"2025-12",{"name":41,"class":42},{"id":290,"slug":291,"hasResults":11,"nctId":292,"briefTitle":293,"officialTitle":294,"acronym":295,"eligibilityCriteria":296,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":297,"targetDuration":4,"studyType":22,"phases":299,"briefSummary":300,"conditions":301,"keywords":304,"overallStatus":91,"whyStopped":4,"lastUpdateSubmitDate":309,"lastUpdatePostDateStruct":310,"startDateStruct":312,"completionDateStruct":314,"leadSponsor":316,"locationsCount":43},"100588233","laughter-yoga-intervention-in-patients-on-haemodialysis-100588233","NCT06938737","Laughter Yoga Intervention in Patients on Haemodialysis","Effects of Laughter Yoga on Happiness, Mental Well-being and Blood Pressure in Hemodialysis Patients: A Randomized Controlled Trial","laughter yoga","Inclusion Criteria:\n\n1. Those receiving hemodialysis treatment at Fethiye Can Dialysis Center with a diagnosis of CKD\n2. 18 years of age and older\n3. Ability to read and understand\n4. Those receiving hemodialysis treatment for six months or longer\n5. Interdialytic fluid intake not more than 5% of total weight\n6. Able to communicate in Turkish\n7. No hearing or vision loss\n8. Patients who volunteer to participate in the study\n\nExclusion Criteria:\n\n1. Those with interdialytic fluid intake greater than 5% of total weight\n2. Those with respiratory system diseases that negatively affect the practice of laughter yoga (COPD, asthma, bronchiectasis, lung infections, etc.)\n3. Those with hearing and vision loss\n4. Those who want to leave the study despite completing the survey questions appropriately\n5. Those who do not agree to participate in the study\n6. Those aged 18 and under\n7. Those who start treatment at another dialysis center\n8. Those who change their renal replacement therapy type -",{"count":298,"type":21},72,[24],"This study was planned as a randomized controlled experimental type and pre-test-post-test design in order to examine the effects of laughter yoga applied to hemodialysis patients on the happiness and mental well-being levels of the patients and on blood pressure.\n\nThe universe of the study will be patients receiving hemodialysis treatment at Fethiye Özel Can Dialysis Center (N=184) and the sample will be a total of 72 patients, consisting of the experimental group (n=36) and the control group (n=36).\n\nAfter obtaining the permission of the ethics committee and institution, the data will be collected face to face by the researchers before and after the laughter yoga to be applied to hemodialysis patients receiving treatment at Fethiye Özel Can Dialysis Center and who agreed to participate in the study. In the collection of data; Introductory Information Form (TBF), Warwick-Edinburgh Mentai Well-Being Scale (WEMİOÖ), Oxford Happiness Scale (OMÖ) and blood pressure measurements of the patients will be used. IBM SPSS 25.0 package program will be used to evaluate the data.",[302,303],"Haemodialysis Patients","Laughter Yoga",[305,295,306,307,308],"Haemodialysis","Happiness","Mental Well-being","blood pressure","2025-04-14",{"date":311,"type":35},"2025-04-22",{"date":313,"type":21},"2025-04-28",{"date":315,"type":21},"2025-06-20",{"name":41,"class":42},{"id":318,"slug":319,"hasResults":11,"nctId":320,"briefTitle":321,"officialTitle":322,"acronym":4,"eligibilityCriteria":323,"healthyVolunteers":141,"sex":16,"minAge":52,"maxAge":324,"enrollmentInfo":325,"targetDuration":4,"studyType":22,"phases":327,"briefSummary":328,"conditions":329,"keywords":331,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":335,"lastUpdatePostDateStruct":336,"startDateStruct":338,"completionDateStruct":340,"leadSponsor":342,"locationsCount":43},"100569685","comparison-of-the-effectiveness-of-different-exercise-types-in-individuals-with-chronic-neck-pain-100569685","NCT06697457","Comparison of the Effectiveness of Different Exercise Types in Individuals with Chronic Neck Pain","Comparison of the Effectiveness of Dynamic Isometric, Static Isometric and Craniocervical Flexor Exercise Training in Individuals with Chronic Neck Pain","Inclusion Criteria:\n\n* Being between the ages of 18 and 55,\n* Scoring 15\u002F50 or less on the Neck Disability Index,\n* Having a history of chronic neck pain for at least 3 months,\n* Having a pain level of 5\u002F10 or more,\n* Showing signs of cervical movement control dysfunction,\n* Having cervical muscle tenderness during physical examination.\n\nExclusion Criteria:\n\n* Being diagnosed with a vascular disease,\n* Being diagnosed with a vestibular disease,\n* Being diagnosed with hypertension,\n* Being diagnosed with fibromyalgia or rheumatoid arthritis,\n* Having had spine surgery in the last 12 months,\n* Having received an exercise program or standard physiotherapy program involving the cervical region in the last 12 months,\n* Having congenital or acquired kyphosis, scoliosis, etc. having postural deformity,\n* Having specific neck pain such as cancer,\n* Having fractures, instability, inflammatory diseases, history of neck trauma, infections, neurological deficit, having spinal diseases such as radiculopathy, spondylosis.","55 Years",{"count":326,"type":21},48,[24],"The aim of this study is to compare the effectiveness of craniocervical flexion, static and dynamic isometric exercise training applied with a conventional physiotherapy program in individuals with chronic neck pain.",[330],"Chronic Neck Pain",[332,333,334],"neck pain","chronic","exercise","2024-11-18",{"date":337,"type":35},"2024-11-20",{"date":339,"type":35},"2024-06-24",{"date":341,"type":21},"2025-02",{"name":41,"class":42},{"id":344,"slug":345,"hasResults":11,"nctId":346,"briefTitle":347,"officialTitle":348,"acronym":4,"eligibilityCriteria":349,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":350,"enrollmentInfo":351,"targetDuration":144,"studyType":111,"phases":4,"briefSummary":353,"conditions":354,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":359,"lastUpdatePostDateStruct":360,"startDateStruct":362,"completionDateStruct":364,"leadSponsor":366,"locationsCount":43},"100545632","subacromial-impingement-syndrome-functional-tests-correlation-with-ultrasound-parameters-100545632","NCT06384430","Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters","Subacromial Impingement Syndrome: The Relationship Between Shoulder Functional Tests and Ultrasound Parameters","Inclusion Criteria:\n\n1. Being between 18-70 years old\n2. Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)\n\nExclusion Criteria:\n\n1. Under 18, over 70 years of age\n2. Those diagnosed with rheumatologic diseases\n3. Those with symptomatic shoulder osteoarthritis\n4. Those with shoulder instability\n5. Shoulder pain in active, passive cervical spine movements\n6. Previous shoulder surgery\n7. Findings of adhesive capsulitis (\\>50% restriction of passive range of motion in 2 planes or detection of a full-thickness rotator cuff tear on ultrasound)\n8. Physiotherapy or intra-articular injection in the last 3 months\n9. Diagnosis of type 2 diabetes or hypothyroidism","70 Years",{"count":352,"type":21},70,"In this study, among the patients who applied to the Physical Medicine and Rehabilitation outpatient clinic of Muğla Training and Research Hospital and were diagnosed with subacromial impingement by anamnesis and clinical tests, inclusion criteria) and exclusion criteria will be included in the study. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated. 4 years of musculoskeletal ultrasound experience will be recorded by a radiologist using ultrasound (Siemens® V8, LA2-14A probe) in modified Crass position (positioning with the palm of the examined side on the posterior iliac wing) by measuring subacromial bursa thickness, supraspinatus tendon thickness, acromiohumeral distance, supraspinatus tendon thickness\u002Facromiohumeral distance ratio. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated.",[355,356,357,358],"Subacromial Impingement Syndrome","Shoulder Tendinitis","Shoulder Bursitis","Shoulder Pain","2024-09-23",{"date":361,"type":35},"2024-09-25",{"date":363,"type":35},"2024-04-01",{"date":365,"type":21},"2024-10-31",{"name":41,"class":42},""]