[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Morehouse School of Medicine\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":161},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,59,87,113,137],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":35,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":47,"lastUpdatePostDateStruct":48,"startDateStruct":51,"completionDateStruct":53,"leadSponsor":55,"locationsCount":58},"100626901","families-implementing-good-health-traditions-for-life-100626901",false,"NCT07441655","Families Implementing Good Health Traditions for Life","FIGHT for Life","Inclusion Criteria:\n\n1. Family 1.a.) Black Parent\u002FGuardian: age 18 years or older residing in the same household with child (i.e., biological or have legal guardianship for child) 1.b.) Child: age 8-15 years old\n2. Parent\u002FGuardian have HbA1c level 5.7-6.4% (prediabetes)\n3. Parent\u002FGuardian willing to commit to participation in a 20-month research study and have no plans to move from the area over the next 20-months\n4. Parent\u002Fchild are ambulatory and able to participate in physical activity\n\nExclusion Criteria:\n\n1. Individuals with severe psychological disorders that may prevent\u002Finterfere with study participation\n2. Physical impairments that may prevent participation in moderate intensity physical activity;\n3. Previous diagnosis of diabetes\n4. History of congestive heart failure, renal failure, or recent (\\\u003C12 months) cardiovascular events such as myocardial infarction or stroke;\n5. Person taking medications that may affect endpoint analyses\n6. Persons with co-morbid contraindications to physical activity or dietary changes.\n7. Currently pregnant or planning to become pregnant in the next year.","ALL","18 Years",{"count":19,"type":20},70,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study will provide evidence for the utility of using a community-engaged research approach to implement a tailored, family-oriented adaptation of the Diabetes Prevention Program that will have positive effects on risk factors associated with type 2 diabetes morbidity and mortality among Black families in a Southwest Georgia community.",[26,27,28,29,30,31,32,33,34],"Diabetes","Chronic Disease","Type 2 Diabetes","Healthy Lifestyle","Nutrition, Healthy","Sedentary Behavior","Family","Family Research","Family and Household",[36,37,38,39,40,41,42,43,44,45],"diabetes","rural","type 2 diabetes","nutrition","physical activity","diabetes prevention","family research","family and household","chronic disease","sedentary behavior","RECRUITING","2026-06-18",{"date":49,"type":50},"2026-06-23","ACTUAL",{"date":52,"type":50},"2026-02-04",{"date":54,"type":20},"2028-04-30",{"name":56,"class":57},"Morehouse School of Medicine","OTHER",1,{"id":60,"slug":61,"hasResults":11,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":65,"eligibilityCriteria":66,"healthyVolunteers":67,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":68,"targetDuration":4,"studyType":21,"phases":70,"briefSummary":72,"conditions":73,"keywords":76,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":58},"100609470","phase-4-cleansing-options-in-out-patient-setting-to-improve-tolerance-coop-sit-trial-100609470","NCT07215000","Cleansing Options in Out-Patient Setting to Improve Tolerance (COOP SIT) Trial","Cleansing Options in Outpatient Setting to Improve Tolerance (COOP SIT) Trial","COOP SIT","Inclusion Criteria:\n\n* Adults over age of 18 years undergoing outpatient colonoscopy for various indications, ability to consent in English or Spanish. Patients will still be allowed to join if there is a history of colorectal cancer or previous surgery\n\nExclusion Criteria:\n\n* Patient is less than 18 years of age, any pregnant or nursing women, unable to consent, or patient is incarcerated.",true,{"count":69,"type":20},300,[71],"PHASE4","The purpose of this research is to compare patient preferences for two bowel preparation options: low-volume tablets (Suflave\u002FSutab) versus the standard colon preparation using Golytely (polyethylene glycol). The study aims to enroll approximately 300 patients, who will be randomly assigned to one of the two preparation methods in a 2:1 ratio prior to their scheduled colonoscopy appointments. Surveys will be conducted both before and after the procedures.\n\nThis project will be conducted over a 12-month period and seeks to compare patient experience of both preparation methods in an outpatient setting. The study will evaluate the rate of preparation completion, patient satisfaction, tolerance of the solutions, and the endoscopic adequacy of each method.\n\nEligible participants are patients aged 18 or older with upcoming colonoscopy appointments who can provide informed consent in English or Spanish. There is no health risks associated with this study, as both bowel preparation methods are FDA-approved and commonly used in clinical practice.",[74,75],"Colorectal Cancer Screening","Bowel Cleansing for Colonoscopy",[77,78],"Colorectal cancer screening","Bowel cleansing for colonoscopy","2025-10-08",{"date":81,"type":50},"2025-10-09",{"date":83,"type":50},"2025-10-01",{"date":85,"type":20},"2027-06",{"name":56,"class":57},{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":92,"acronym":4,"eligibilityCriteria":93,"healthyVolunteers":67,"sex":94,"minAge":95,"maxAge":96,"enrollmentInfo":97,"targetDuration":4,"studyType":21,"phases":99,"briefSummary":100,"conditions":101,"keywords":103,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":58},"100533704","comparing-effectiveness-of-physician-assisted-versus-self-assisted-pap-smear-collection-100533704","NCT06229275","Comparing Effectiveness of Physician-assisted Versus Self-assisted Pap Smear Collection","A Study to Evaluate the Effectiveness of the Rover Cervex-Brush Device vs. the Personal Pap Smear Device™ for Collection of Cervical Cells for Detecting Cervical Dysplasia or Neoplasia","Inclusion Criteria:\n\n* Adult women, aged 21-65 years old.\n* Do not have any medical or psychiatric condition affecting the ability to give voluntary informed consent.\n* Be able to read and understand English\n\nExclusion Criteria:\n\n* Participants currently on menses\n* Inability to provide Informed Consent\n* Previous total hysterectomy\n* History of radiation treatment for cervical cancer\n* Pregnancy\n* Medical condition that interferes with conduct of study, in investigator's opinion\n* Evidence of active cervical infection requiring treatment\n* Known bleeding diathesis","FEMALE","21 Years","65 Years",{"count":98,"type":20},200,[23],"This purpose of this research study is to determine the effectiveness of the Personal Pap Smear Device™ to collect adequate cervical cell samples for cytology examination when compared with the Rover Cervex-Brush (Cervix-Examination Brush).",[102],"Cervical Cancer Screening",[104],"pap smear collection","2025-07-16",{"date":107,"type":50},"2025-07-20",{"date":109,"type":50},"2024-07-25",{"date":111,"type":20},"2026-03-30",{"name":56,"class":57},{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":117,"acronym":118,"eligibilityCriteria":119,"healthyVolunteers":67,"sex":16,"minAge":17,"maxAge":120,"enrollmentInfo":121,"targetDuration":4,"studyType":21,"phases":123,"briefSummary":125,"conditions":126,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":136},"100515096","phase-2-involving-communities-in-addressing-the-maternal-health-crisis-making-an-impact-100515096","NCT05987059","Involving Communities in Addressing the Maternal Health Crisis: Making an IMPACT","Project IMPACT","Inclusion Criteria:\n\n* Self-identify as Black\u002F African-American\n* Fluent English-Speaker\n* Not pregnant at the time of enrollment\n* Own a phone\n* Receive services at the community-based site\n\nExclusion Criteria:\n\n\\-","44 Years",{"count":122,"type":20},850,[124],"PHASE2","With support from the National Heart, Lung, and Blood Institute, The Center for Maternal Health Equity at Morehouse School of Medicine is conducting a research study to test the implementation of Pre-Pregnancy Counseling in community-based settings.",[127],"Preconception Health","2025-06-12",{"date":130,"type":50},"2025-06-15",{"date":132,"type":50},"2024-01-01",{"date":134,"type":20},"2028-12",{"name":56,"class":57},2,{"id":138,"slug":139,"hasResults":11,"nctId":140,"briefTitle":141,"officialTitle":142,"acronym":143,"eligibilityCriteria":144,"healthyVolunteers":67,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":145,"targetDuration":147,"studyType":148,"phases":4,"briefSummary":149,"conditions":150,"keywords":4,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":153,"lastUpdatePostDateStruct":154,"startDateStruct":156,"completionDateStruct":158,"leadSponsor":160,"locationsCount":58},"100424283","morehouse-total-cancer-care-protocol-100424283","NCT04804878","Morehouse Total Cancer Care Protocol","Morehouse Total Cancer Care Protocol: A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer","MSMTCC","Inclusion Criteria:\n\n1. 18 years of age and older.\n2. Diagnosed with cancer, or at risk for cancer. This includes anyone in the general population, but our primary focus will be on patients with a cancer diagnosis.\n3. Able to understand and sign the TCCP Informed Consent and Research Authorization form directly or through an authorized representative. The Informed Consent and Research Authorization will be available in both English and Spanish languages\n\nExclusion Criteria:\n\nNone\n\n\\-",{"count":146,"type":20},5000,"5 Years","OBSERVATIONAL","The overall objective of the Morehouse Total Cancer Care study is to develop an improved standard of cancer care by facilitating new biomarker and drug target discovery, informatics solutions, clinical trials, and \"personalized medicine\" for our community oncology partners (i.e., community hospital systems, and other cancer care providers). To bring new translational research to the community, Morehouse School of Medicine has initiated the Total Cancer Care Program (TCCP). The TCCP establishes a unique collection of blood, tissue, other biological samples and their associated data (survey data, medical records data, cancer registry data, and other related data) from thousands of African American cancer patients, survivors, or those at risk of having cancer. This is not a treatment trial, but a longitudinal study designed to create a centralized cancer biorepository for precision medicine.",[151,152],"Cancer","Cancer Risk","2021-03-16",{"date":155,"type":50},"2021-03-18",{"date":157,"type":50},"2018-04-05",{"date":159,"type":20},"2037-04",{"name":56,"class":57},""]