[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Université du Québec à Chicoutimi\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":93},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,62],{"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":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":49,"whyStopped":4,"lastUpdateSubmitDate":50,"lastUpdatePostDateStruct":51,"startDateStruct":54,"completionDateStruct":56,"leadSponsor":58,"locationsCount":61},"100593162","nature-based-intervention-for-chronic-pain-in-older-people-100593162",false,"NCT07002853","Nature-based Intervention for Chronic Pain in Older People","Nature-based Intervention Program for Sustainable Health in Older People Living With Chronic Non-specific Lower Back Pain (PARC Project 2) - A Feasibility Trial","PARC-2","Inclusion Criteria:\n\n* Aged 65 years +\n* Having low back pain for 3 months or more\n* Being able to walk independently\n* Mental state \\>25\u002F30 in the MMSE questionnaire\n* Frailty score \\\u003C3\u002F5 (Fried criterias)\n\nExclusion Criteria:\n\n* Presenting other severe musculoskeletal, cardiovascular, or neurological conditions, or systemic diseases (e.g., cancer).","ALL","65 Years",{"count":20,"type":21},15,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn if a nature-based intervention program has positive effects on the physical and psychosocial health in a group of older participants with chronic non-specific lower back pain. The main questions it aims to answer are:\n\nWill the program improve:\n\n* The physical outcomes such as mobility, strength and balance?\n* The psychosocial health outcomes?\n\nParticipants will:\n\n* Be assessed before and after the program;\n* Participate in one session per week of the intervention.",[27,28,29],"Chronic Disease","Chronic Pain (Back \u002F Neck)","Older Adults (65 Years and Older)",[31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48],"Aging","Chronic pain","Non-specific low back pain","Nature-based interventions","Falls","Forest bathing","Shinrin-yoku","Social","Nature connectedness","Functionning","Physical activity","Mindfulness","Meditation","Rehabilitation","Postural control","Strength","Quality of life","Balance","RECRUITING","2025-05-24",{"date":52,"type":53},"2025-06-04","ACTUAL",{"date":55,"type":53},"2025-05-22",{"date":57,"type":21},"2026-12-01",{"name":59,"class":60},"Université du Québec à Chicoutimi","OTHER",1,{"id":63,"slug":64,"hasResults":11,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":4,"eligibilityCriteria":68,"healthyVolunteers":69,"sex":17,"minAge":70,"maxAge":4,"enrollmentInfo":71,"targetDuration":4,"studyType":22,"phases":73,"briefSummary":74,"conditions":75,"keywords":78,"overallStatus":49,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":61},"100577256","evaluation-and-treatment-of-adhesive-capsulitis-using-non-invasive-neurostimulation-devices-100577256","NCT06795932","Evaluation and Treatment of Adhesive Capsulitis Using Non-invasive Neurostimulation Devices","Prise En Charge Des Atteintes Proprioceptives Chez Une Population Avec Capsulite Rétractile","Inclusion Criteria:\n\n* 18 years old and over\n* Good general health\n* Adhesive capsulitis (experimental group) or\n* No shoulder pain (placebo group)\n\nExclusion Criteria:\n\n* Cognitive disorders;\n* Any neurological disease\u002Finjury affecting the upper limbs;\n* History or diagnosis of muscle, tendon, or capsular tear;\n* Shoulder surgery\u002Fprosthesis;\n* Pregnant woman;\n* Presence of metal in the skull or jaw;\n* History of epilepsy.",true,"18 Years",{"count":72,"type":21},30,[24],"The goal of this randomized controlled trial is to compare the integrity of somatosensory processing with transcranial magnetique stimulation (TMS) and corticospinal excitability of the affected shoulder in individuals with adhesive capsulitis versus healthy controls.\n\nThe secondary objective is to compare the clinical and neurophysiological effects of an intervention using tendon vibration (VIB) to induced kinesthetic illusions. This will involve comparing two groups: one receiving a real intervention versus a placebo intervention protocol, both coupled with standardized exercises in individuals with capsulitis. The hypotheses are that the proprioceptive processing and corticospinal excitability are impaired in the presence of capsulitis, and that the VIB + exercises intervention will result in greater improvements than the placebo VIB + exercises.\n\nTo goal is to establish the first empirical foundations for understanding adhesive capsulitis, using cutting-edge neurophysiological investigation technologies.\n\nTMS will be used to explore the presence of maladaptive plasticity in motor networks by assessing the excitability and integrity of the primary motor cortex (M1) and the corticospinal tract.\n\nRecruitement:\n\n30 healthy participants and 30 participants with a diagnosis of adhesive capsulitis will undergo 2 baselines assesments, 6 interventions with tendon vibration and 2 follow-up evaluation. Participants will be age- and sex-matched.\n\nBaseline and follw-up include:\n\n* Questionnaires : SPADI, QuickDASH, French version of the Mcgill Pain Questionnaire;\n* Active and passive range of motion;\n* Ultrasound for diagnosing capsulitis.\n\nComparison parameters:\n\n* active motor threshold (aMT)\n* Motor evoked potential (MEP) latency and amplitude\n* Standardized kinesthetic illusion procedure (SKIP) : direction of illusion, clearness, amplitude\u002Fspeed.\n\nInterventions :\n\n* 2 baselines including all questionnaires, ultrasound, active and passive range of motion, TMS procedure and SKIP;\n* 2 VIB interventions per week, for 3 weeks\n\n  * Real VIB : 80Hz of vibration to induce kinesthetic illusions,\n  * Placebo VIB : 40Hz of vibration that does not induce kinesthetic illusions\n* 2 follow-up including all questionnaires, ultrasound, active and passive range of motion, TMS procedure and SKIP.",[76,77],"Adhesive Capsulitis of the Shoulder","Frozen Shoulder",[79,80,81,82,83,84],"Adhesive Capsulitis","Frozen shoulder","Tendon Vibration","Transcranial Magnetique Stimulation","Proprioception","Kinesthetic illusions","2025-01-27",{"date":87,"type":53},"2025-01-28",{"date":89,"type":53},"2024-10-17",{"date":91,"type":21},"2027-04",{"name":59,"class":60},""]