[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100647866":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":15,"centralContacts":20,"locations":25,"responsibleParty":45,"collaborators":10,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":10,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":55,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":10,"studyType":61,"phases":10,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":70,"whyStopped":10,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"National Institutes of Health Clinical Center (CC)","NIH",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"Healthy Volunteers",null,"Individuals screened under this protocol who are determined to be in good health and without a pain history that would classify them as a participant with pain. These participants may be considered for future NCCIH studies as healthy controls.",{"label":13,"type":10,"description":14,"interventionNames":10},"Participants With Pain","Individuals screened under this protocol who have a current or prior pain history or pain symptoms identified through medical history, examination, questionnaires, or sensory testing. These participants may be considered for future NCCIH studies of pain and related processes.",[16],{"name":17,"affiliation":18,"role":19},"Miroslav Backonja, M.D.","National Center for Complementary and Integrative Health (NCCIH)","PRINCIPAL_INVESTIGATOR",[21],{"name":17,"role":22,"phone":23,"phoneExt":10,"email":24},"CONTACT","(301) 402-5679","misha.backonja@nih.gov",[26],{"facility":27,"status":10,"city":28,"state":29,"zip":30,"country":31,"countryCode":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"National Institutes of Health Clinical Center","Bethesda","Maryland","20892","United States","US",{"type":34,"coordinates":35},"Point",[36,37],-77.10026,38.98067,{"lat":37,"lon":36},[40],{"name":41,"role":22,"phone":42,"phoneExt":43,"email":44},"NIH Clinical Center Office of Patient Recruitment (OPR)","800-411-1222","TTY dial 711","ccopr@nih.gov",{"type":46,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100647866","screening-protocol-100647866",false,"NCT07712874","Screening Protocol","Screening Evaluation of Volunteers for Studies of Pain","* INCLUSION CRITERIA:\n\nTo be eligible to participate in this study, an individual must meet all of the following criteria:\n\n* Stated interest in, and availability for, participating in NCCIH studies and willingness to comply with the procedures of this protocol.\n* At least 12 years of age\n* No identified acute health concerns (i.e. symptomatic uncontrolled diabetes mellitus, congestive heart failure, liver cirrhosis, ongoing cancer (excluding skin basal cell carcinoma and squamous cell carcinoma) as evidenced by screening medical history\n* Ability to understand and able to provide written informed consent form.\n\nEXCLUSION CRITERIA:\n\nAn individual who meets any of the following criteria will be excluded from participation in this study:\n\n* Have active medical or psychiatric health issues that create additional and substantial adverse risks related to study procedures. Medical examples are the acute complications of medical disease, such as asymptomatic hypertensive urgency, diabetic ketoacidosis, symptomatic hyperthyroidism, and unstable angina. Psychiatric examples are the acute complications of psychiatric disease, such as acute mania, paranoid delusions, or having active panic attacks.\n* Ongoing substance uses disorder or illicit substance use\n* Pregnancy\n\nAdditional exclusion from optional QST procedures:\n\nHas a major medical condition or medical history that in a clinician's assessment could affect heat sensitivity, pain thresholds, or ability to comply with study procedures. This may include cardiovascular, autonomic, or neurological conditions (including stroke and blindness or deafness, a history of brain damage, or psychosis).",true,"ALL","12 Years","100 Years",{"count":59,"type":60},10000,"ESTIMATED","OBSERVATIONAL","This study is a screening evaluation for volunteers who are interested in participating in National Center for Complementary and Integrative Health (NCCIH) research studies about pain and related processes, such as emotion, mood, and decision-making. Screening may include review of medical history, physical exam, vital signs, questionnaires, blood and urine tests, and optional sensory testing to better understand pain and related symptoms. The purpose is to identify and characterize healthy volunteers and people with pain who may be eligible for future NCCIH research studies. This screening study does not test a treatment and has no formal hypothesis.",[64],"Pain",[66,9,67,68,69],"Pain screening","Quantitative Sensory Testing","Ecological Momentary Assessment","Patient-Reported Outcomes","NOT_YET_RECRUITING","2026-08-20",{"date":73,"type":74},"2026-08-21","ACTUAL",{"date":76,"type":60},"2026-08-26",{"date":78,"type":60},"2050-07-02",{"name":18,"class":6},1]