[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100591740":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":29,"centralContacts":33,"locations":42,"responsibleParty":58,"collaborators":25,"id":61,"slug":62,"hasResults":63,"nctId":64,"briefTitle":65,"officialTitle":66,"acronym":67,"eligibilityCriteria":68,"healthyVolunteers":63,"sex":69,"minAge":70,"maxAge":25,"enrollmentInfo":71,"targetDuration":25,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":85,"overallStatus":44,"whyStopped":25,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},{"fullName":5,"class":6},"Neuroscience Research Australia","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Pain education and clinical hypnosis delivered via a mobile app","EXPERIMENTAL","Pain education and clinical hypnosis for self-managing back pain, delivered via a mobile app.",[13],"Behavioral: Pain education and clinical hypnosis delivered via a mobile app",{"label":15,"type":16,"description":17,"interventionNames":18},"Guideline-informed factsheet","ACTIVE_COMPARATOR","A guideline-informed factsheet for back pain, delivered via a webpage.",[19],"Behavioral: Guideline-informed factsheet",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Pain education and clinical hypnosis will be delivered via a mobile app. The 8-week intervention includes daily sessions on pain education and clinical hypnosis for managing back pain (5 minutes of education, 15 minutes of listening to hypnotherapy audio and engaging in physical\u002Fsocial activities for 5 minutes). The first six weeks will be semi-standardised, with participants following a set program with the option to repeat sessions. The last two weeks will be flexible, allowing participants to choose a specific program or self-paced continuation of the intervention. Adherence will be monitored by tracking the number of days participants complete sessions, as recorded by the mobile app.",[9],null,{"type":22,"name":15,"description":27,"armGroupLabels":28,"otherNames":25},"A single guideline-informed factsheet for back pain delivered via a webpage. Participants will be informed that the factsheet intends to provide reassurance for their back pain and encourage reflections on treatments and self-management options.",[15],[30],{"name":31,"affiliation":5,"role":32},"James H McAuley, PhD","PRINCIPAL_INVESTIGATOR",[34,38],{"name":31,"role":35,"phone":36,"phoneExt":25,"email":37},"CONTACT","+61293991266","j.mcauley@neura.edu.au",{"name":39,"role":35,"phone":40,"phoneExt":25,"email":41},"Rodrigo RN Rizzo, PhD","(02) 9399 1000","r.rizzo@neura.edu.au",[43],{"facility":5,"status":44,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":56},"RECRUITING","Randwick","New South Wales","2031","Australia","AU",{"type":51,"coordinates":52},"Point",[53,54],151.24895,-33.91439,{"lat":54,"lon":53},[57],{"name":31,"role":35,"phone":36,"phoneExt":25,"email":37},{"type":32,"investigatorFullName":59,"investigatorTitle":60,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"James McAuley","Principal Investigator","100591740","digitally-delivered-treatments-to-reduce-chronic-low-back-pain-100591740",false,"NCT06984354","Digitally Delivered Treatments to Reduce Chronic Low Back Pain","NOTUS Trial: A Randomised Controlled Trial of Two Digitally Delivered Treatment Options for Chronic Back Pain","NOTUS","Inclusion Criteria:\n\n* Experiencing non-specific chronic low back pain (LBP), defined as pain between the 12th rib and the buttock crease.\n* LBP with or without leg pain (in case of leg pain, LBP is worse than leg pain).\n* Currently consulting with a general practitioner for their non-specific chronic LBP across Australia.\n* Mean pain intensity score on the Numeric Rating Scale ≥ 3\u002F10 in the past week.\n* A score of at least moderate on question 8 of the physical functioning component of the SF-36 questionnaire.\n* Access to a mobile device with minimal requirements to download the study app (300MB).\n* An internet connection to access the mobile app functionalities.\n* Able to understand English via reading and audio materials.\n\nExclusion Criteria:\n\n* Known or suspected specific spinal (e.g., radiculopathy, fracture) or specific non-spinal non- (e.g., tumour, infection) pathology.\n* Less than six months post-spinal surgery.\n* Scheduled for major surgery during the program or the follow-up period.\n* Known or suspected serious psychiatric condition not being treated by a health professional that would impact adherence to the trial activities.\n* Known or suspected sight or hearing problems that would limit access to the intervention components (reading and listening using headphones).","ALL","18 Years",{"count":72,"type":73},720,"ESTIMATED","INTERVENTIONAL",[76],"NA","This study aims to evaluate the effectiveness of pain education and clinical hypnosis delivered via a mobile app compared to a guideline-informed factsheet for reducing pain and disability in people experiencing chronic low back pain attending general practice.",[79,80,81,82,83,84],"Low Back Pain","Chronic Pain (Back \u002F Neck)","General Practice (GP), Primary Care Settings","Digital Health","Hypnosis, Chronic Pain Management","Patient Education",[86,82,87,88,89],"Back Pain","Hypnosis","Pain Education","Chronic Pain","2025-07-16",{"date":92,"type":93},"2025-07-20","ACTUAL",{"date":95,"type":93},"2025-06-02",{"date":97,"type":73},"2028-05-26",{"name":5,"class":6},1]