[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"delayed-onset-muscle-soreness-doms\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:delayed-onset-muscle-soreness-doms":70},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"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":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100649443","real-world-evidence-of-cannabinoid-for-observed-pain-relief-100649443",false,"NCT07733791","Real-world Evidence of Cannabinoid for Observed Pain Relief","Topical Use of Cannabinoids (CBD:THC 3:1) as Adjunctive Therapy for Chronic Muscle Pain in Athletes: A Comparative Prospective Observational Study","RECOVER","Inclusion Criteria:\n\n* Predominantly articular, bone, or non-muscular pain (e.g., fractures, degenerative arthropathies)\n* Presence of open skin lesions, infections, or active dermatoses at the topical application site\n* Current use of WADA-prohibited substances that may interfere with outcome assessment\n* Athletes in official competition during the study period using THC-containing formulations (due to WADA in-competition prohibition)\n* Severe acute musculoskeletal injury (complete muscle rupture, fracture) within the last 30 days\n* Cognitive or technological inability to use the follow-up platform\n\nExclusion Criteria:\n\n* Predominantly articular, bone, or non-muscular pain (e.g., fractures, degenerative arthropathies)\n* Presence of open skin lesions, infections, or active dermatoses at the topical application site\n* Current use of WADA-prohibited substances that may interfere with outcome assessment\n* Athletes in official competition during the study period using THC-containing formulations (due to WADA in-competition prohibition)\n* Severe acute musculoskeletal injury (complete muscle rupture, fracture) within the last 30 days\n* Cognitive or technological inability to use the follow-up platform","ALL","18 Years",{"count":20,"type":21},60,"ESTIMATED","90 Days","OBSERVATIONAL","Chronic muscle pain is one of the most prevalent clinical challenges in sports medicine, significantly affecting training capacity, competitive performance, and quality of life in athletes.\n\nThe endocannabinoid system has emerged as a promising therapeutic target for pain modulation in the sports context.\n\nThis prospective, comparative, non-randomized observational study aims to evaluate whether adjuvant topical application of a cannabinoid balm (CBD:THC 3:1 - Papa \\& Barkley) provides additional reduction in chronic muscle pain intensity in athletes, compared to systemic CBD oil alone, over 90 days of follow-up in a real-world clinical practice setting.\n\nSixty adult athletes (amateur or professional) with established chronic muscle pain (≥3 months) who receive clinical indication for cannabinoid therapy will be followed in two observational cohorts: Cohort A (n=30), receiving only systemic CBD oil (60 mg\u002Fday oral\u002Fsublingual), and Cohort B, (n=30) receiving systemic CBD oil plus the topical cannabinoid balm (CBD:THC 3:1, applied twice daily to the affected muscle area).\n\nTreatment allocation is based exclusively on the clinical decision of the principal investigator, reflecting routine medical practice. The primary outcome is the change in Brief Pain Inventory (BPI) scores from baseline (D0) to end of follow-up (D90). Secondary outcomes include pain intensity (NRS), sleep quality (PSQI), quality of life (SF-36), perceived muscle recovery (TQR scale), functional capacity (LEFS\u002FUEFI), rescue analgesic use, and safety\u002Ftolerability of the topical formulation.\n\nThe study aims to generate real-world evidence on the effectiveness and safety of adjuvant topical cannabinoid therapy in athletes with chronic muscle pain in the Brazilian clinical practice setting.",[26,27],"Chronic Musculoskeletal Pain","Delayed Onset Muscle Soreness (DOMS)",[29,30],"Topical Cannabinoids","Systemic Cannabidiol","NOT_YET_RECRUITING","2026-07-29",{"date":34,"type":35},"2026-07-30","ACTUAL",{"date":37,"type":21},"2027-01-01",{"date":39,"type":21},"2027-07-01",{"name":41,"class":42},"Associação Pan-Americana Multidisciplinar de Endocanabinologia","OTHER",{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":17,"minAge":18,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":69},"100609816","effects-of-a-5-week-probiotic-supplementation-intervention-on-markers-of-delayed-onset-muscle-soreness-100609816","NCT07219498","Effects of a 5-Week Probiotic Supplementation Intervention on Markers of Delayed Onset Muscle Soreness","Inclusion Criteria:\n\n* complete a minimum of 150 minutes a week of at least moderate intensity exercise in either an endurance-based or resistance-based training style based on a self-reported physical activity over the past month\n* good general health with no injuries or health conditions that would affect physical activity\n* willing to abstain from consistent NSAID use and other probiotic supplements over the course of this study\n\nExclusion Criteria:\n\n* known musculoskeletal injuries or physical limitations that could interfere with performing the designated physical activity required\n* underlying conditions that could place them at an increased risk during exercise such as cardiovascular, respiratory, or metabolic diseases\n* currently take a probiotic supplement, are prescribed and taking an antibiotic during the intervention, or report using NSAIDs or steroids within the recovery time window\n* report using an NSAID more than twice a week on a regular basis",true,"30 Years",{"count":52,"type":21},24,"INTERVENTIONAL",[55],"NA","The purpose of this study is to evaluate how probiotic supplementation (PS) influences post-exercise recovery in healthy, physically active young adults. Researchers aim to determine if the Lactobacillus casei probiotic strain reduces symptoms of delayed onset muscle soreness (DOMS) based on perceived muscle soreness, pressure pain threshold, and power output following exercise induced muscle damage (EIMD).",[58,27],"Exercise Induced Muscle Damage","RECRUITING","2026-04-30",{"date":62,"type":35},"2026-05-04",{"date":64,"type":35},"2026-02-05",{"date":66,"type":21},"2026-12-31",{"name":68,"class":42},"University of Minnesota",1,"Delayed Onset Muscle Soreness, DOMS"]