[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Cambridge Health Alliance\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":232},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,41,69,93,128,162,185,211],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100559501","improving-mental-health-treatment-for-individuals-in-crisis-interacting-with-the-criminal-legal-system-100559501",false,"NCT06564948","Improving Mental Health Treatment for Individuals in Crisis Interacting With the Criminal-Legal System","Inclusion Criteria:\n\n1. Treatment as Usual (TAU) arm\n\n   1. Cambridge Health Alliance (CHA) patients from the cities other than Cambridge considered to be in the \"catchment area\" of CHA (Everett, Chelsea, Somerville, Medford, Malden, and Winthrop)\n   2. Ages 18-100\n   3. Identified as having police involvement between 2009 and 2025. Treatment as Usual patients will be identified using \"targeted limited chart review methods\" used in our prior studies, \"scraping\" clinical notes in the Electronic Health Records for criminal legal involvement. Initial Identification terms, \"police\", \"arrest\", \"court\", \"summons\", \"jail\", and \"crime\" will be used to identify candidates for police involvement, downloading the sentence in which the keyword appeared and the sentence before and after. Next, an iterative process of editing of the search terms will be conducted to remove patients with negation of the keyword (\"did not commit a crime\"), and other sentence characteristics that generate false positives (\"cardiac arrest\"). Samples of the resulting dataset will be taken, accuracy assessed by examining the surrounding sentences, leading to further iterations and repetition of the process until a high level of accuracy is achieved.\n2. FSJS arm\n\n   1. Cambridge Health Alliance patients from Cambridge\n   2. Ages 18-100\n   3. Individuals who have come into contact with the Cambridge Police Department (as identified in the FSJS data) between 2009 and 2025.\n3. FSJS+Navigator arm\n\n   1. Recruited during the study period in the CHA ED\n   2. Ages 18-100\n   3. Individuals who are brought into the Emergency Department under police supervision (excluding individuals currently incarcerated)\n\n      * involuntarily brought to the Emergency Department for psychiatric evaluation because they are considered to be a risk to themselves or others (MA Law 123(12)); or\n      * the subject of a police call for service for a mental health issue who are willingly admitted to the Emergency Department\n\nExclusion Criteria\n\n1. Treatment as Usual (TAU) arm\n\n   1. Cambridge Health Alliance patients residing in the City Cambridge are excluded from the TAU arm\n   2. Under the age of 18\n   3. Individuals with no identified criminal legal system contact during the study time period (no criminal legal involvement found in the targeted limited chart review method).\n   4. Any individual incarcerated at the Middlesex Jail\u002FPrison that has not been released by the end of the period of data collection (December 31, 2025).\n2. FSJS arm\n\n   1. Cambridge Health Alliance patients outside of Cambridge will be excluded from the FSJS arm\n   2. Under the age of 18\n   3. Any individual incarcerated at the Middlesex Jail\u002FPrison that has not been released by the end of the period of data collection (December 31, 2025)\n3. FSJS+Navigator arm\n\n   1. Under the age of 18\n   2. Any individual who becomes incarcerated during the course of the study\n   3. Individuals who enter the Emergency Department not under police supervision\n\n      * For example, individuals will be excluded who voluntarily come to the ED seeking psychiatric care because they feel they may be a risk to themselves or others\n      * Individuals brought to the ED from a jail or court ordered to the ED as an alternative to jail or prison","ALL","18 Years","100 Years",{"count":19,"type":20},1040,"ESTIMATED","INTERVENTIONAL",[23],"NA","The proposed Center will leverage burgeoning real-time data linkage capabilities among health systems, Medicaid payors, and criminal legal (e.g., jail booking data, jail release data) systems, to identify individuals coming in and out of jail for suicide assessment and prevention, and to better coordinate care across these disparate systems. This Center will advance the fields of suicide prevention and criminal legal system-based mental health by solving a well-known, central problem in both fields: the inability to track and intervene with individuals moving in and out of both and often multiple systems. The goal is near-term reductions in the U.S. suicide rate.",[26,27],"Suicide Risk","Psychiatric Disorders","RECRUITING","2026-06-02",{"date":31,"type":32},"2026-06-04","ACTUAL",{"date":34,"type":32},"2025-02-01",{"date":36,"type":20},"2027-09-30",{"name":38,"class":39},"Cambridge Health Alliance","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":15,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":56,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":40},"100632683","exploring-the-effects-of-brief-mindfulness-training-with-vagal-nerve-stimulation-on-alcohol-cue-reactivity-among-young-adult-heavy-drinkers-100632683","NCT07516873","Exploring the Effects of Brief Mindfulness Training With Vagal Nerve Stimulation on Alcohol Cue Reactivity Among Young Adult Heavy Drinkers","Exploring the Feasibility and Acceptability of Brief Mindfulness Training With Vagal Nerve Stimulation for Reducing Alcohol Consumption Among Young Adults","Inclusion Criteria:\n\n* Currently living in Massachusetts.\n* Aged 21-29 years old.\n* Consume either more than 14 standard drinks of alcohol per week OR at least 5 standard drinks in one day per week (in past 30 days).\n* Have sufficient English fluency to understand procedures and questionnaires.\n* Have the capacity and ability to provide informed consent.\n* Scores at least 15 points on the PACS at screening. Participants who score between 10 and 14 pts will undergo additional doctoral-level review to assess eligibility.\n\nExclusion Criteria:\n\n* Current or past diagnosis of a substance use disorder based on the Quick Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) Module C (Substance Use Disorders).\n* Active prescription for sedative\u002Fhypnotics, opioids, or anesthetic medications.\n* Active prescription for medications used to treat alcohol use disorder (AUD), e.g., naltrexone, disulfiram, acamprosate, etc.\n* Active psychosis or schizophrenia-spectrum disorder diagnosis.\n* Bipolar I disorder history or severe level of mania.\n* Severe symptoms of PTSD.\n* Acute suicidality or self-injurious behavior.\n* Cognitive inability as demonstrated by the inability to complete an informed consent assessment with \\>90% accuracy after 2 attempts.\n* Current participation in another experimental intervention research study.\n* Current daily mindfulness practice \\>10 minutes per day.\n* Participation in an 8-week intensive Mindfulness-Based Intervention or residential meditation retreat in past 3 years.\n* Expected medical hospitalization in the next 2 months; or are currently pregnant.\n* Expected incarceration in the next 2 months.\n* Presence of electronic implants, such as heart pacemakers, defibrillators, or pumps.\n* Presence of a cardiac rhythm disorder.\n* History of seizures.\n* Presence of skin disorders or malignant diseases in the area in or around the left ear.\n* Lack of alcohol craving as assessed by the PACS during screening (score of \\\u003C 10 points).","21 Years","29 Years",{"count":51,"type":20},50,[23],"The present study will assess the acceptability and feasibility of a brief intervention designed to help young heavy drinkers reduce their alcohol consumption. All participants will complete a brief (1-week) mindfulness intervention, and participants will be randomized to receive either active or inactive Respiratory-gated Auricular Vagal Afferent Nerve Stimulation (RAVANS) during two in-person laboratory visits. Heart rate variability data and self-report survey data will be collected to assess the impact of the intervention on autonomic regulation, alcohol consumption, and additional clinical measures.",[55],"Heavy Drinking",[55,57,58,59,60],"Mindfulness","Vagus Nerve Stimulation","Alcohol Cue Reactivity","Heart Rate Variability","2026-05-08",{"date":63,"type":32},"2026-05-12",{"date":65,"type":32},"2026-03-06",{"date":67,"type":20},"2026-08",{"name":38,"class":39},{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":76,"sex":15,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":4,"studyType":21,"phases":81,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":40},"100632402","the-effectiveness-and-acceptability-of-formal-versus-informal-mindful-self-compassion-for-adolescents-100632402","NCT07513220","The Effectiveness and Acceptability of Formal Versus Informal Mindful Self-Compassion for Adolescents","Formal Versus Informal Mindful Self-Compassion Programming for Adolescents","Inclusion Criteria:\n\n* Be 14-19 years of age for the duration of the study;\n* If 14-17 years of age: have a parent with sufficient literacy skills to understand the consent process and have the ability to provide written informed consent, and have sufficient English fluency and literacy skills themselves to understand the assent process, procedures, and questionnaires and have the ability to provide written assent;\n* If 18-19 years of age: have sufficient English fluency and literacy skills themselves to understand the consent process, procedures, and questionnaires and have the ability to provide written informed consent;\n* Have access to the internet and an electronic device with adequate data capacity to complete questionnaires online and attend online videoconference groups;\n* Be available and willing to attend the scheduled online videoconference groups for 4 weeks and complete the online assessments.\n\nExclusion Criteria:\n\n* Current or past-year treatment with mindfulness-based psychotherapy (e.g., MBCT, DBT, or ACT);\n* Current or past-year participation in a mindfulness- or compassion-based program;\n* A routine of, on average, 10 minutes of mindfulness practice per day over the past 30 days (greater than or equal to 300 minutes);\n* Simultaneous participation in another experimental research study;\n* Current or past-year diagnosis of: schizophrenia spectrum or other psychotic disorder, bipolar 1 disorder, or severe substance\u002Falcohol use disorder;\n* Current or past-month suicidal ideation;\n* Hospitalization for reasons related to mental health within the past 6 months;\n* Recent modifications to psychiatric medication(s) (within the last 30 days or within the last 90 days for antidepressants (e.g., SSRI, SNRI, etc.);\n* Inability to complete consent\u002Fassent process or baseline assessment.",true,"14 Years","19 Years",{"count":80,"type":20},135,[23],"The goal of this clinical trial is to learn if two types of mindful self-compassion programs work to improve coping in adolescents. The investigators will also learn about adolescents' liking of, and the other potential mental health and academic benefits of, these programs. The main questions this clinical trial aims to answer are:\n\n* Do two types of mindful self-compassion programs improve coping in adolescents?\n* Do two types of mindful self-compassion programs improve mental health (e.g., stress, anxiety, depression) and academic outcomes (e.g., academic engagement) in adolescents?\n* How satisfactory are two types of mindful self-compassion programs for adolescents?\n\nTo do this, the investigators will compare adolescents who complete two types of mindful self-compassion programs to adolescents in a \"waitlist control\" condition (who complete no study tasks during the program period, but will have the opportunity to complete the program at the end of the study).\n\nParticipants will:\n\n* Complete a brief phone interview to confirm their eligibility (15 min)\n* Complete an online survey including questions about coping, mental health, and academic engagement (30 min)\n* Complete a live, online, four-week-long mindful self-compassion program OR no study tasks during this four-week period (if randomly assigned to a waitlist condition)\n* Complete an online survey 1 week after the 4-week period, including questions about coping, mental health, and academic engagement, as well as their liking of the program they completed (if applicable)\n* Complete an online survey 1 month after the 4-week period, including questions about coping, mental health, and academic engagement\n* (Waitlist condition only) Have the opportunity to complete one of the two mindful self-compassion programs after the study had ended",[84],"Coping","2026-04-15",{"date":87,"type":32},"2026-04-20",{"date":89,"type":32},"2026-04-13",{"date":91,"type":20},"2027-04-30",{"name":38,"class":39},{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":99,"eligibilityCriteria":100,"healthyVolunteers":11,"sex":101,"minAge":16,"maxAge":102,"enrollmentInfo":103,"targetDuration":4,"studyType":21,"phases":104,"briefSummary":105,"conditions":106,"keywords":108,"overallStatus":119,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":40},"100584563","frefghterft-lifestyle-coaching-interventions-for-obese-firefighters-firefit-100584563","NCT06890975","\"F!reF!ghterF!t\": Lifestyle Coaching Interventions for Obese Firefighters (FireFit)","\"F!reF!ghterF!t\": A Randomized Controlled Trial of Lifestyle Coaching Interventions for Obese Firefighters","FireFit","Inclusion Criteria:\n\n* Male firefighters aged 18-60 years\n* Currently active as volunteer or career firefighters\n* Body mass index (BMI) ≥30 kg\u002Fm² based on self-reported height and weight\n* Express interest in participating in a clinical study aimed at improving body composition (weight loss), metabolic status, and quality of life\n* Residing and\u002For working in Massachusetts, Rhode Island, or Southern New Hampshire (Boston metro area)\n\nExclusion Criteria:\n\n* Female sex\\*\n* BMI \\\u003C30 kg\u002Fm² based on self-reported height and weight\n* Active psychosis\n* History or diagnosis (during the RCT) of any of the following:\n\nMajor cardiovascular disease event (e.g., myocardial infarction, cardiac arrest, cerebrovascular accident) Cancer (excluding non-melanoma skin cancer) Abnormal liver function (aminotransferase, bilirubin, or alkaline phosphatase ≥3× the upper limit of normal) Renal dysfunction (estimated glomerular filtration rate ≤30 mL\u002Fmin\u002F1.73 m²)\n\n* Current or recent (within 6 months) use of testosterone treatment or anti-obesity\u002Fobesogenic medications\n* Unwillingness to adhere to potential intervention assignments\n\n  * Because this is an exploratory study, the number of subjects is limited, and men make up roughly 85% of the US fire service, the current proposal is limited to men. In future studies, we will include women firefighters.","MALE","60 Years",{"count":51,"type":20},[23],"Our goal is to explore the effectiveness of 9- month lifestyle medicine based coaching intervention (individual and group coaching) versus control (usual care\u002F written health instructions). The primary study outcomes will be mean changes in body composition metrics . Secondary outcomes will be the prevalence of metabolic abnormities, progression\u002Fregression of Metabolic Syndrome, push-up \\& sit\u002Fstand capacity, self-reported physical activity, and quality of life\u002Fdiet\u002Fsleep measures.",[107],"Obesity and Obesity-related Medical Conditions",[109,110,111,112,113,114,115,116,117,118],"obesity","firefighters","diabetes mellitus","coaching","healthy lifestyle","lifestyle medicine","metabolic syndrome","quality of life","mental health","physical fitness","NOT_YET_RECRUITING","2026-02-19",{"date":122,"type":32},"2026-02-23",{"date":124,"type":20},"2026-04-21",{"date":126,"type":20},"2026-12",{"name":38,"class":39},{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":132,"acronym":4,"eligibilityCriteria":133,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":102,"enrollmentInfo":134,"targetDuration":4,"studyType":21,"phases":136,"briefSummary":137,"conditions":138,"keywords":145,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":40},"100592056","pilot-study-of-bottarga-supplementation-a-little-known-sustainable-blue-food-100592056","NCT06988462","Pilot Study of \"Bottarga\" Supplementation: A Little-known, Sustainable \"Blue\" Food","* Adults aged 18-60 years\n* Residents of Massachusetts\n* Presence of at least one metabolic abnormality (low HDL cholesterol, elevated LDL cholesterol, elevated triglycerides, obesity, or HbA1c ≥ 5.7%) or a diagnosis of diabetes\n* Not pregnant\n* Willing to consume a nutritional supplement and comply with study procedures\n\nExclusion Criteria:\n\n* Use of any medications for diabetes (except metformin), dyslipidemia (except statins), or immunosuppression\n* Current use of any supplements containing n-3 fatty acids\n* Current use of illicit drugs (other than marijuana)\n* Use of hormone therapy (except oral contraceptives)\n* Known allergies to fish, seafood, or any fish-derived products, including bottarga\n* Pregnancy\n* Clinical evidence or history of hepatic or renal insufficiency\n* Immunodeficiency conditions\n* History of non-skin cancer\n* Participation in other clinical research studies",{"count":135,"type":20},20,[23],"This pilot study aims to explore the potential benefits of consuming Greek bottarga (grey mullet fish roe) in individuals with at least one metabolic abnormality (low HDL cholesterol, high LDL cholesterol, high triglycerides, obesity, or HbA1c ≥ 5.7%) or a diagnosis of diabetes.\n\nBefore initiating the crossover randomized controlled trial (RCT), the investigators will conduct a preliminary dose-testing study in five adults with at least one metabolic abnormality. Participants will undergo clinical assessments before and after the dietary intervention to evaluate changes in metabolic health markers. Following this phase, the investigators will proceed with a randomized, controlled crossover trial involving 20 eligible adult participants. This main study phase will compare the metabolic effects of daily bottarga supplementation with those of a calorically matched dairy product over an 8-week intervention period, with a 2-week washout period between interventions.\n\nThe investigators anticipate that bottarga supplementation will improve lipid profiles, inflammation markers, and insulin resistance, thereby supporting the potential use of sustainable blue foods as part of a healthy diet.",[139,140,141,142,143,144],"Prediabetes","Diabetes","High Cholesterol\u002FHyperlipidemia","Obesity & Overweight","Triglycerides","HDL Cholesterol",[146,147,148,149,150,151,152,153,154],"Bottarga","pre diabetes","inflammation","sustainability","nutritional intervention","overweight","metabolic abnormalities","lipid profile","diabetes","2026-02-17",{"date":120,"type":32},{"date":158,"type":32},"2025-10-17",{"date":160,"type":20},"2026-12-01",{"name":38,"class":39},{"id":163,"slug":164,"hasResults":11,"nctId":165,"briefTitle":166,"officialTitle":167,"acronym":4,"eligibilityCriteria":168,"healthyVolunteers":11,"sex":15,"minAge":169,"maxAge":16,"enrollmentInfo":170,"targetDuration":4,"studyType":21,"phases":172,"briefSummary":173,"conditions":174,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":40},"100566990","family-connections-100566990","NCT06662357","Family Connections","Family Connections: A Community-Based Approach to Expanding Mental Health Access and Engagement for SED Youth","Inclusion Criteria:\n\n* 3 through 18 years (17½ years maximum at time of enrollment)\n* Referred by Primary Care Physician's (PCP) from one of the three Cambridge Health Alliance (CHA) primary care intervention sites to the Family Connections team for an integrated child mental health and\u002For substance use disorder clinical assessment.\n* Positive screen on CHA's standard pediatric mental health and substance use screening instruments, and\u002For parental concern about possible mental health\u002Fsubstance use needs, and\u002For PCP concern about possible mental health\u002Fsubstance use needs\n* Enrolled in MassHealth\n\nExclusion Criteria:\n\n* Subjects over 17.5 years (SAMHSA data collection required at 6 and 12 months after enrollment which must occur before age 18 years.)\n* Youth who are not enrolled in MassHealth\n* CHA patients with PCP located at CHA primary care site other than the identified intervention sites","3 Years",{"count":171,"type":20},300,[23],"The Family Connections study, is intended to disrupt disparities in mental health treatment access for children at-risk for childhood trauma (ACEs) and\u002For serious emotional disturbance (SED). \"Family Connections\" will use mobile clinical and family support teams to improve mental health outcomes. This clinical innovation, nested in an integrated system-of-care will be piloted for children, ages 3-18 yrs., with SED who receive primary care through Cambridge Health Alliance.",[175,176],"Emotional Disturbance","Behavior Disorders in Children","2025-06-25",{"date":179,"type":32},"2025-06-26",{"date":181,"type":32},"2025-01-30",{"date":183,"type":20},"2028-09-29",{"name":38,"class":39},{"id":186,"slug":187,"hasResults":11,"nctId":188,"briefTitle":189,"officialTitle":190,"acronym":191,"eligibilityCriteria":192,"healthyVolunteers":11,"sex":15,"minAge":193,"maxAge":194,"enrollmentInfo":195,"targetDuration":4,"studyType":21,"phases":197,"briefSummary":198,"conditions":199,"keywords":4,"overallStatus":119,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":205,"startDateStruct":206,"completionDateStruct":208,"leadSponsor":210,"locationsCount":4},"100548330","screening-and-support-for-youth-sasy-100548330","NCT06419595","Screening and Support for Youth (SASY)","Screening and Support for Youth","SASY","Inclusion Criteria:\n\n* 12 to 17 year old teens\n\nExclusion Criteria:\n\n* younger than 12 or older than 17","12 Years","17 Years",{"count":196,"type":20},220,[23],"To adapt the Screening and Support for Youth (SASY) intervention and approach to recruitment for racial, ethnic and linguistic diverse youth aged 12-17 in the Denver Health catchment area",[200,201,202,203],"Adolescent Health","Minority Health","Mental Health","Community Health Services","2025-06-23",{"date":179,"type":32},{"date":207,"type":20},"2026-11-01",{"date":209,"type":20},"2028-03-31",{"name":38,"class":39},{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":4,"eligibilityCriteria":217,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":218,"targetDuration":4,"studyType":21,"phases":220,"briefSummary":221,"conditions":222,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":224,"lastUpdatePostDateStruct":225,"startDateStruct":227,"completionDateStruct":229,"leadSponsor":231,"locationsCount":40},"100555733","our-whole-lives-gemini-virtual-integrative-medical-group-visits-for-managing-chronic-pain-100555733","NCT06515925","Our Whole Lives Gemini: Virtual Integrative Medical Group Visits for Managing Chronic Pain","Phase II: GEMINI: Virtual Integrative Medical Group Visits for Managing Chronic Pain","Inclusion Criteria:\n\n* English-speaking adults\n* Over the age of 18\n* Experiencing chronic musculoskeletal pain. (Pain may have more than one source; Pain must be non-malignant; Participant must have an average pain intensity of ≥ 4 (1 out of 10) in the past 7 days; Participant must meet the chronic criteria of a pain problem that has persisted at least 3 months, and has resulted in pain on at least half the days in the past 6 months)\n\nExclusion Criteria:\n\n* Inability to understand English at a level necessary for informed consent and understanding participation instructions, and participating in the group;\n* Serious underlying systemic or co-morbid conditions or life event that precludes physical or cognitive ability to participate in the study.\n* Severe depression\n* Current mania or psychosis;\n* Active heroin or cocaine use in the past 3 months\n* Heavy alcohol use\n* Known or planned pregnancy",{"count":219,"type":20},212,[23],"The goal of this research study is to test the efficacy of a non-prescription medicine, web-based platform solution for patients with chronic pain, to improve pain self-management and related outcomes. The main question investigators aim to answer is; would the use of this web-based intervention plus an online group visit compared to control result in better pain-related outcomes and improved pain impact?",[223],"Chronic Pain","2025-03-12",{"date":226,"type":32},"2025-03-13",{"date":228,"type":32},"2024-08-01",{"date":230,"type":20},"2025-11-30",{"name":38,"class":39},""]