[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Universitat de les Illes Balears\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":101},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,72],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100593897","muscle-injury-rtp-design-in-football-effects-of-backward-design-vs-forward-design-100593897",false,"NCT07012408","Muscle Injury RTP Design in Football; Effects of Backward Design vs Forward Design.","Muscle Injury Return To Play Design in Football; Effects of Backward Design Versus Forward Design . A Randomized Controlled Trial","MIRTPD","Inclusion Criteria:\n\n* Male soccer players.\n* Diagnosed with a muscle injury via magnetic resonance imaging (MRI) during the three year study period.\n* They will all belong to the same club.\n* Age will be between 18 and 40 years old.\n\nExclusion Criteria:\n\n* Patients (Muscle injuries) that do not cause players to miss training or competitions.\n* Patients voluntarily decide not to participate in the study or abandon the RTP process due to transfers or other exceptional causes.","MALE","18 Years","40 Years",{"count":21,"type":22},74,"ESTIMATED","INTERVENTIONAL",[25],"NA","Introduction\n\n\"Return-to-play\" (RTP) is an English term that corresponds to \"return to competition\". It is important to understand that this return is a constant, dynamic, and personalized decision-making process . The main objective of RTP is not to predict the exact moment of an athlete's return; rather, it is to prevent new injuries. For this, adequate decision-making is necessary. There are several important steps in the process, including correct diagnosis, strict control of workloads, and intelligent management of modifiers intrinsic to the sport that can lead to anxiety and stress\n\nHow are the pieces of the RTP puzzle arranged and managed?\n\nHow are RTP processes evaluated today?\n\nHow should RTP be understood? Should it be understood statically, as a checklist, or as a constant decision-making process involving the player?\n\nMain objective: Evaluate the design of the RTP process for muscle injuries in sports.\n\nSpecific objectives:\n\n* To compare two RTP designs and evaluate how their design influences the anxiety experienced by the player.\n* Identify variables that may be altered when choosing a regressive or progressive RTP design, such as sleep quality and cortisol level.\n* To establish direction in the design of the RTP process.\n* Create complete clinical guidelines on muscle injuries in sports with a focus on RTP design.\n\nMaterial and Methods\n\nDefinition of the Study Subjects\n\nThe subjects of the study will be all players belonging to the first or B team who suffer a muscle injury diagnosed by magnetic resonance imaging. At the time of injury, they will be randomly assigned to either the control group (following a regressive RTP design) or the intervention group (following a progressive RTP design). Masking will be double-blind. The sample size will be N=74.\n\nThe secondary variables will be recorded in the database after diagnosis by MRI. Subsequently, the primary variables will be measured and recorded at the beginning, middle, and end of the RTP period.\n\nIt is estimated that approximately half of the necessary sample size has been reached: about 37 subjects with muscle injury. The first statistical analysis will then be carried out to observe the preliminary results.\n\nAfter three years, once the analysis has been completed, the results and conclusions will be written up for publication in a journal.",[28,29],"Muscle Injuries","Football Players",[31,32,33],"Return to play","Design","effects","NOT_YET_RECRUITING","2025-06-14",{"date":37,"type":38},"2025-06-18","ACTUAL",{"date":40,"type":22},"2025-09-01",{"date":42,"type":22},"2028-09-01",{"name":44,"class":45},"Universitat de les Illes Balears","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":55,"minAge":18,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":23,"phases":59,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":46},"100577148","therapeutic-exercise-through-exergames-on-mobile-devices-for-cervical-rehabilitation-100577148","NCT06794528","Therapeutic Exercise Through Exergames on Mobile Devices for Cervical Rehabilitation","A Randomized Two-Arm Clinical Trial, Fixed-Assignment Study on Adherence to Therapeutic Exercise in Cervical Rehabilitation Using A Serious Game In Mobile Devices","RehbeCa","Inclusion Criteria:\n\n* Persons of legal age with cervicalgia.\n* Have a smart mobile device (smartphone or tablet) on which to download the App.\n\nExclusion Criteria:\n\n* Acute musculoskeletal pathological processes or exacerbation (less than 15 days of evolution). Includes presentation of symptoms such as paraesthesia, radiating pain, loss of strength in the upper limb.\n* Episodes of severe pain more than 15 days of evolution.\n* Accident with cervical or dorsal injury within the last month.\n* Refusing to sign the informed consent.\n* Not having a device suitable for installation or lack of experience in the use of smart mobile devices.\n* Baseline NDI score of less than 5.\n* Presence of red flags:\n\n  * Suspicion of fracture: advanced age, previous trauma, osteoporosis.\n  * Suspicion of neurological involvement: loss of sensation in extremities, loss of strength or muscle mass.\n  * Suspicion of infection: fever, night sweats.\n  * Suspicion of cancer: Previous history of cancer, no improvement in one month of treatment, weight loss, headache, vomiting.\n  * Suspicion of systemic disease: headache, fever, malaise, general headache, fever, malaise, unilateral skin rash (herpes).","ALL","70 Years",{"count":58,"type":22},60,[25],"The objective of this study is to determine whether performing cervical therapeutic exercises using a serious game through a mobile application enhances treatment adherence compared to performing the same exercises at home following standard practice.",[62],"Neck Pain","RECRUITING","2025-01-26",{"date":66,"type":38},"2025-01-28",{"date":68,"type":38},"2025-01-16",{"date":70,"type":22},"2025-05",{"name":44,"class":45},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":55,"minAge":18,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":23,"phases":82,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},"100575395","phase-2-multicenter-study-protocol-research-on-evaluation-and-detection-of-surgical-wound-complications-with-ai-based-recognition-redscar-trial-100575395","NCT06771726","Multicenter Study Protocol: Research on Evaluation and Detection of Surgical Wound Complications with AI-based Recognition. (REDSCAR-trial)","Multicenter Study Protocol: Research on Evaluation and Detec-tion of Surgical Wound Complications with AI-based Recogni-tion. (REDSCAR-trial)","REDSCAR","Inclusion Criteria:\n\n* Participants must have signed an informed consent.\n* Participants must be over 18 years of age.\n* Participants must have undergone either urgent or scheduled surgery performed via laparotomy or laparoscopy.\n* Participants need access to a smartphone capable of downloading the app with android OS.\n* Either the participant or a close family member must be able to operate the app effectively.\n* Participants must be able to attend follow-up consultations at the surgical outpatient clinic after discharge, one week post-surgery, or earlier if the app flags a potential infection.\n\nExclusion Criteria:\n\n* Patients who lack access to a smartphone or are unable to properly use the app.\n* Patients unfamiliar with mobile devices or unable to comprehend the app's functionality or questions.\n* Patients who did not provide informed consent.\n* Patients who are unable to comply with the follow-up requirements.",{"count":81,"type":22},168,[83,84],"PHASE2","PHASE3","The increasing use of telemedicine in surgical care has demonstrated significant poten-tial for improving patient outcomes and optimizing healthcare resources. This study investigates the efficacy of the RedScar© app in telematic detection and monitoring of surgical site infections (SSIs), a major cause of healthcare-associated infections (HAIs) with significant economic and health impacts. RedScar© leverages a patient's smartphone to provide automated infection risk assessments without requiring clini-cian input, offering a potential solution for remote postoperative care. In a pilot study, RedScar© demonstrated 100% sensitivity and 83.13% specificity in detecting SSIs, with high patient satisfaction regarding its comfort, cost-effectiveness, and ability to reduce absenteeism. This multicenter prospective study aims to validate these findings, com-paring app-based detection with in-person evaluations. Primary objectives include as-sessing the sensitivity and specificity of RedScar© using receiver operating character-istic (ROC) analysis, while secondary objectives include evaluating patient satisfaction and standardizing telematic follow-up across centers. The study will include 168 pa-tients undergoing abdominal surgery, with follow-up assessments conducted remotely via the app and in-person at specified intervals. Data will be analysed using descrip-tive and statistical methods to assess diagnostic accuracy and patient satisfaction. This research seeks to further develop RedScar© as a reliable, scalable tool for enhancing postoperative care, reducing healthcare costs, and improving patient experiences in surgical recovery.",[87],"Surgical Wound Infection",[89,90,91,92],"surgical wound infection","Telemedicine","smartphone application","artificial intelligence",{"date":94,"type":38},"2025-01-20",{"date":96,"type":38},"2024-01-01",{"date":98,"type":22},"2025-12",{"name":44,"class":45},5,""]