[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100586923":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":34,"centralContacts":12,"locations":38,"responsibleParty":59,"collaborators":12,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":12,"eligibilityCriteria":66,"healthyVolunteers":67,"sex":68,"minAge":69,"maxAge":70,"enrollmentInfo":71,"targetDuration":12,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":80,"overallStatus":41,"whyStopped":12,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"University of Nottingham","OTHER",[8,13,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","NO_INTERVENTION","Participants continue with their usual exercise regime.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Runner Group","EXPERIMENTAL","Particpants follow an 8 week intervention including aerobic elements (running), a schedule of gradually intensitfing strengthening exercises and flexibility exercises.",[18],"Behavioral: Runner group",{"label":20,"type":15,"description":21,"interventionNames":22},"Swim\u002FCycle group","Particpants follow an 8 week intervention including aerobic elements (swim\u002Fcycle), a schedule of gradually intensitfing strengthening exercises and flexibility exercises.",[23],"Behavioral: Swim\u002FCycle Group",[25,30],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":12},"BEHAVIORAL","Runner group","The intervention groups undertake 8 weeks of a combined exercise programme including aerobic elements (running), a schedule of gradually intensifying strengthening exercises and flexibility exercises",[14],{"type":26,"name":31,"description":32,"armGroupLabels":33,"otherNames":12},"Swim\u002FCycle Group","The intervention groups undertake 8 weeks of a combined exercise programme including aerobic elements (swim\u002Fcycle), a schedule of gradually intensitfing strengthening exercises and flexibility exercises",[20],[35],{"name":36,"affiliation":5,"role":37},"Kimberley Edwards","PRINCIPAL_INVESTIGATOR",[39],{"facility":40,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"University of Nottingham, Queen's Medical Centre","RECRUITING","Nottingham","Notts","NG7 2UH","United Kingdom","UK",{"type":48,"coordinates":49},"Point",[50,51],-1.15047,52.9536,{"lat":51,"lon":50},[54],{"name":55,"role":56,"phone":57,"phoneExt":12,"email":58},"Professor Sport Exercise and Nutrition Education","CONTACT","+44 1157486500","kimberley.edwards@nottingham.ac.uk",{"type":37,"investigatorFullName":36,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"100586923","a-combined-exercise-programme-involving-strengthening-flexibility-and-aerobic-exercise-for-lower-back-pain-100586923",false,"NCT06921694","A Combined Exercise Programme Involving Strengthening, Flexibility and Aerobic Exercise for Lower Back Pain","A Combined Exercise Programme Involving Strengthening, Flexibility and Aerobic Exercise for Lower Back Pain: a Randomised-controlled Study","Inclusion Criteria:\n\n* Aged 18-45 years\n* Participant is willing and able to give informed consent for participation in the study\n* Suffering from chronic NSLBP (more than 3 months, localised below the costal margin and above the gluteal folds)\n* Suffers from pain or functional limitations as a result of their LBP (minimum VAS (back) score of 3\u002F10 or ODI score of at least 5\u002F50 or RMD score of at least 5\u002F24 (note, unlike ODI, RMD does not describe specific cuts offs for different levels of disability)\n* Able to exercise\n\nExclusion Criteria:\n\n* Radiating pain to leg \u002F sciatica \u002F acute radiculopathy\n* Specific diagnosis\u002Fcondition for LBP (e.g. herniated disk, degenerative disk disease, spondylolysis, spinal stenosis, spinal tumour, facet joint damage)\n* History of osteoporosis , arthritis, scoliosis, or kyphosis.\n* Current spinal infection, cancer or a current fracture (any bone).\n* History of spinal\u002Fback surgery\n* Unable to participate in physical activity and exercise\n* Pregnant or breast feeding\n* History of substance abuse\n* History of psychiatric illness (eg. depression, dementia, schizophrenia) for which currently taking medication\n* History or current neurological condition (e.g. epilepsy)\n* Not in possession or have access to adapted equipment (phone, computer, functioning WIFI)\n* Unable to understand and communicate in English\n* Having taken part in a research study in the last 3 months involving invasive procedures or an inconvenience allowance",true,"ALL","18 Years","45 Years",{"count":72,"type":73},88,"ESTIMATED","INTERVENTIONAL",[76],"NA","This randomised controlled trial will evaluate the effectiveness of different exercise modalities for individuals with low back pain. Participants will be allocated to one of three groups: a control arm (usual exercise), a running-based intervention, or a swimming\u002Fcycling-based intervention. Outcomes related to pain and function will be measured at baseline, 8 weeks, and 12 months.",[79],"Low Back Pain, Chronic",[81,82],"chronic non specific low back pain","exercise intervention","2025-12-04",{"date":85,"type":86},"2025-12-12","ACTUAL",{"date":88,"type":86},"2025-04-01",{"date":90,"type":73},"2026-09-30",{"name":5,"class":6},1]