[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"reliability\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:reliability":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,43,69,90,113],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100618314","inter--and-intra-observer-reliability-of-the-iowa-level-of-assistance-scale-and-the-effect-of-staff-retraining-100618314",false,"NCT07330011","Inter- and Intra-Observer Reliability of the Iowa Level of Assistance Scale and the Effect of Staff Retraining","Inter- and Intra-observer Reliability of the Iowa Level of Assistance (ILoA) Scale for Measuring Postoperative Functional Recovery in Orthopedic Patients: an Observational Study","ILOA","Inclusion Criteria:\n\n* For Observers (Physiotherapists):\n\nAll physiotherapists working at the main Istituto Ortopedico Rizzoli (IOR) site in Bologna or at the two satellite sites in Argenta and Bagheria.\n\nPhysiotherapists must have the role of observers in the study. All physiotherapists affiliated with the SAITeR service who have previously received initial training in the use of the ILoA scale; newly hired staff must have completed the specific training pathway.\n\nFor Patients:\n\nPatients admitted to IOR Bologna or Argenta for whom administration of the ILoA scale is part of routine clinical practice.\n\nPatients undergoing primary hip or knee arthroplasty for osteoarthritis. Patients undergoing revision hip or knee arthroplasty. Patients undergoing hip arthroplasty or osteosynthesis for femoral fracture.\n\nExclusion Criteria:\n\n* Refusal or inability to provide informed consent (for both physiotherapists and patients).","ALL","18 Years",{"count":20,"type":21},42,"ESTIMATED","OBSERVATIONAL","The aim of this study is to evaluate, in routine clinical practice, the inter- and intra-observer reliability of the Iowa Level of Assistance (ILoA) scale, which is regularly used to assess functional recovery in orthopedic patients. A secondary objective is to investigate the impact of a structured retraining program for healthcare staff on the use of the ILoA scale and to determine whether this intervention influences the reliability indices of the scale.",[25,26,27],"Joint Replacement","Functional Recovery","Reliability",[29],"ILOA scale","RECRUITING","2026-01-08",{"date":33,"type":34},"2026-01-09","ACTUAL",{"date":36,"type":34},"2025-11-15",{"date":38,"type":21},"2026-09",{"name":40,"class":41},"Istituto Ortopedico Rizzoli","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":17,"minAge":18,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":4},"100602351","angle-specific-torque-profile-analysis-in-the-wrist-joint-100602351","NCT07122375","Angle-Specific Torque Profile Analysis in the Wrist Joint","Reliability and Normative Results of Angle-Specific Torque Profile Analysis in the Wrist Joint","Inclusion Criteria:\n\n* Healthy young adult participants\n\nExclusion Criteria:\n\n* Participants who were unable to complete the target range of motion\n* Participants with missing data",true,"35 Years",{"count":53,"type":21},50,"The wrist joint performs various tasks at multiple angles during daily activities, both in flexion and extension positions. Among the parameters that facilitate these tasks, strength-particularly in relation to coordination and motor control-plays a key role. Therefore, identifying potential strength deficits is important for maintaining the continuity of daily functional tasks. In the literature, a wide range of methods exist for evaluating strength, from manual tests to advanced technological devices (references). One such method, isokinetic dynamometry, is considered among the most reliable due to its ability to provide objective and standardized measurements across different types of muscle contractions (isometric, isotonic, and isokinetic). Isokinetic dynamometers yield various data including peak torque, average torque, total work, fatigue index, and torque slope. Researchers frequently interpret findings based on peak or average torque values generated during isokinetic contractions. These torque measures provide an overall representation of strength during a given movement.\n\nIn wrist movements, rather than a single muscle, muscle groups are responsible for executing motion. However, when only peak or average torque at a single joint angle is assessed, the presence or absence of weakness in the movement can be detected, but it offers limited information. If weakness exists, identifying the specific joint angle at which it occurs can provide more direct insights into which muscles may be impaired. Furthermore, angle-specific profiling allows for characterization of muscle behavior throughout the movement, offering valuable information about potential kinematic disruptions. Having normative data on these profiles enables the detection of deviations from typical patterns across the full range of motion, which can be beneficial for both diagnosis and treatment planning.\n\nHowever, to derive such benefits, it is critical that the data be obtained using reliable methods. Reliability refers to the degree to which an instrument or technique yields consistent results across repeated measurements, and is a prerequisite for usability. Statistical Parametric Mapping (SPM) is an increasingly popular method that enables angle-specific torque analysis, providing clinically and scientifically meaningful information on muscle strength. Angle-specific mapping is considered the \"gold standard\" because it presents torque values across the entire joint range, eliminating the need for interpolation between angles. For example, during daily activities, the wrist joint commonly operates within a range from 40° extension to 38° flexion. Therefore, measuring strength at only one joint angle may not be sufficient to reflect the potential limitations experienced in everyday tasks.\n\nDespite its advantages, no reliability study involving SPM analysis has been found for the wrist joint. Furthermore, there is currently no study providing normative data for SPM-based analysis in the wrist. The aim of this study is to examine the reliability of angle-specific torque profile analysis during wrist flexion and extension movements and to provide normative data for healthy young adults.",[56,27,57,58],"Wrist","Torque","Isokinetic","NOT_YET_RECRUITING","2025-08-12",{"date":62,"type":34},"2025-08-14",{"date":64,"type":21},"2025-09-01",{"date":66,"type":21},"2025-12-01",{"name":68,"class":41},"Gazi University",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":50,"sex":17,"minAge":18,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":78,"conditions":79,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":4},"100579911","test-retest-reliability-of-myocene-100579911","NCT06830447","Test-retest Reliability of Myocene","Test-retest Reliability of Low-frequency Fatigue Assessed Using Myocene","Inclusion Criteria:\n\n* active individuals\n\nExclusion Criteria:\n\n* injured participants\n* unhealthy volunteers","40 Years",{"count":53,"type":21},"The test retest reliability of Myocene will be tested.",[27,80],"Fatigue","2025-02-11",{"date":83,"type":34},"2025-02-17",{"date":85,"type":21},"2025-03",{"date":87,"type":21},"2025-05",{"name":89,"class":41},"University of Maia",{"id":91,"slug":92,"hasResults":11,"nctId":93,"briefTitle":94,"officialTitle":95,"acronym":4,"eligibilityCriteria":96,"healthyVolunteers":11,"sex":17,"minAge":97,"maxAge":98,"enrollmentInfo":99,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":100,"conditions":101,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":42},"100566482","craniocervical-dysfunction-index-in-patients-with-temporomandibular-joint-dysfunction-100566482","NCT06655753","Craniocervical Dysfunction Index in Patients With Temporomandibular Joint Dysfunction","Turkish Validity and Reliability of the Craniocervical Dysfunction Index in Patients Temporomandibular Joint Dysfunction","Inclusion Criteria:\n\n* Between the ages of 20-60 years\n* Clinical diagnosis of non-specific neck pain\n* Being able to communicate in Turkish\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Over 60 years of age\n* Those with impairments in cervical mobility that affected the postural assessment","20 Years","60 Years",{"count":53,"type":21},"The aims of this study were to perform cultural adaptation of the Craniocervical Dysfunction Index in patients with Temporomandibular Joint Dysfunction, reliability and validity of the index Turkish speaking adults.",[102,103,27,104],"Temporomandibular Joint Dysfunction","Craniocervical Dysfunction","Validity","2025-02-07",{"date":81,"type":34},{"date":108,"type":21},"2025-03-01",{"date":110,"type":21},"2025-10-01",{"name":112,"class":41},"Alanya Alaaddin Keykubat University",{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":118,"acronym":4,"eligibilityCriteria":119,"healthyVolunteers":50,"sex":17,"minAge":18,"maxAge":120,"enrollmentInfo":121,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":123,"conditions":124,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":42},"100520282","turkish-version-of-digital-eye-strain-questionnaire-desq-100520282","NCT06054542","Turkish Version of Digital Eye Strain Questionnaire (DESQ)","Validity and Reliability of the Turkish Version of Digital Eye Strain Questionnaire (DESQ)","Inclusion Criteria:\n\n* Between the ages of 18-65 years\n* People who spend two or more continuous hours a day on their digital devices (computer, tablet, smartphone) or use more than one device\n\nExclusion Criteria:\n\n* History of ophthalmic surgery or active ocular disease\n* Participants who did not understand the instructions or did not sign a consent form were excluded","65 Years",{"count":122,"type":21},130,"The aims of this study were to perform cultural adaptation of the DESQ and provide information regarding the factor structure, reliability and validity of the instrument in Turkish speaking adults.",[125,27,104,126,127],"Cultural Adaptation","Adults","Eye Strain","2024-10-11",{"date":130,"type":34},"2024-10-15",{"date":132,"type":34},"2023-10-30",{"date":134,"type":21},"2024-12",{"name":112,"class":41}]