[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100572010":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":29,"centralContacts":33,"locations":38,"responsibleParty":56,"collaborators":25,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":64,"eligibilityCriteria":65,"healthyVolunteers":66,"sex":67,"minAge":68,"maxAge":69,"enrollmentInfo":70,"targetDuration":25,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":81,"overallStatus":41,"whyStopped":25,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"University of Graz","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group (No BioStrength Training)","ACTIVE_COMPARATOR","Participants in the Active Comparator group will undergo a conventional strength training program using standard gym machines. Training sessions will occur 3 times per week for 12 weeks. The goal is to compare the outcomes of BioStrength training with traditional strength training.",[13],"Device: Conventional training",{"label":15,"type":16,"description":17,"interventionNames":18},"BioStrength training","EXPERIMENTAL","Participants in the Intervention Group will undergo BioStrength training using Technogym equipment. The intervention will last for 12 weeks, with sessions conducted 3 times per week",[19],"Device: BioStrength Intervention",[21,26],{"type":22,"name":23,"description":17,"armGroupLabels":24,"otherNames":25},"DEVICE","BioStrength Intervention",[15],null,{"type":22,"name":27,"description":11,"armGroupLabels":28,"otherNames":25},"Conventional training",[9],[30],{"name":31,"affiliation":5,"role":32},"Martin Atia","PRINCIPAL_INVESTIGATOR",[34],{"name":31,"role":35,"phone":36,"phoneExt":25,"email":37},"CONTACT","+436642524153","m.atia@edu.uni-graz.at",[39],{"facility":40,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"CF Leibnitz","RECRUITING","Leibnitz, Styria","Styria","8430","Austria","AT",{"type":48,"coordinates":49},"Point",[50,51],15.53836,46.78161,{"lat":51,"lon":50},[54],{"name":31,"role":35,"phone":55,"phoneExt":25,"email":37},"06642524153",{"type":57,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR","100572010","effect-of-biostrength-training-on-muscle-strength-and-satisfaction-in-adults-aged-30-65-100572010",false,"NCT06727695","Effect of BioStrength Training on Muscle Strength and Satisfaction in Adults Aged 30-65","A Comparative Study of Training Effectiveness: Technogyms Biostrength Devices Vs. Conventional Strength Training Devices: a Randomized Controlled Trial","BIO-STR","Inclusion Criteria:\n\n* • Age between 30 and 65 years\n\n  * Healthy individuals without significant medical conditions\n  * Less than 6 months of prior strength training experience\n  * Willing and able to participate in a 12-week training program\n  * Capable of performing strength training exercises such as leg press and chest press\n  * Able to provide written informed consent\n\nExclusion Criteria:\n\n* • History of coronary heart disease\n\n  * History of stroke\n  * Need for changes in antihypertensive treatment within 3 months prior to study start\n  * Arthritis\n  * Pregnancy or less than three months postpartum\n  * Pain and movement restrictions\n  * Use of medications that affect muscle strength or performance (e.g., anabolic steroids, beta-2 agonists, glucocorticoids, statins, benzodiazepines, ACE inhibitors, angiotensin-II receptor blockers, diuretics)\n  * Any medical condition preventing participation in planned endurance and strength training",true,"ALL","30 Years","65 Years",{"count":71,"type":72},42,"ESTIMATED","INTERVENTIONAL",[75],"NA","This study aims to evaluate the effectiveness of Technogyms BioStrength equipment compared to traditional strength training equipment over a 12-week intervention period. The study will determine whether BioStrength machines produce more effective results in terms of muscle strength and body composition. Participants will be allocated to either the BioStrength group or the traditional training group using a minimisation technique to balance important prognostic factors such as handgrip strength, age and gender between the groups. Key measurements include maximum strength tests (10RM) for leg press and chest press, handgrip strength using a dynamometer, and body composition using bioimpedance analysis. Circumference measurements will also be taken. The study will assess whether BioStrength equipment provides superior results in muscle strength, body composition and training efficiency compared to conventional gym equipment.",[78,79,80],"Muscle Strength","Body Composition","Physical Fitness",[82,83,84,85,86,87,88,89,90,91],"Strength training","Muscle strength","Body composition","Customer satisfaction","BioStrength","Technogym","Resistance training","Fitness equipment","Handgrip strength","Randomized controlled trial","2024-12-05",{"date":94,"type":95},"2024-12-11","ACTUAL",{"date":97,"type":95},"2024-10-08",{"date":99,"type":72},"2025-10-01",{"name":5,"class":6},1]