[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of South Dakota\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":112},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,68,92],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100640548","a-mobile-web-app-intervention-to-promote-cervical-cancer-screening-100640548",false,"NCT07574190","A Mobile Web App Intervention to Promote Cervical Cancer Screening","A Mobile Web App Intervention to Promote Cervical Cancer Screening Among Indigenous Women","wPap","Inclusion Criteria:\n\n* Women who are self-identified AI women of the YST in SD\n* Women who are aged 25 to 65 years\n* Women who have not received any of the following cervical cancer screening tests: a Pap test within the past 3 years, primary HPV testing within the past 5 years, or HPV\u002FPap co-testing within the past 5 years.\n* Women who are willing to use their own mobile phone, iPad, tablets, and computers, or a mobile phone borrowed from the research team for the wPap intervention.\n\nExclusion Criteria:\n\n* Women younger than 25 years or older than 65 years\n* Women who are currently up to date with cervical cancer screening according to recommended guidelines (Pap test within the past 3 years, primary HPV testing within the past 5 years, or HPV\u002FPap co-testing within the past 5 years)\n* Women with a prior diagnosis of cervical cancer\n* Women who have had a total hysterectomy that included removal of the cervix, without a history of high-grade precancerous lesions\n* Women with a previous colposcopy examination indicating abnormal cytology that requires more frequent screening than every 3 years",true,"FEMALE","25 Years","65 Years",{"count":22,"type":23},120,"ESTIMATED","INTERVENTIONAL",[26],"NA","The overarching goal of this study is to increase cervical cancer (CC) screening rates among Indigenous women in the U.S. Specifically, the study aims to develop and evaluate a culturally tailored, multilevel, multimedia mobile web app intervention (wPap) for women of the Yankton Sioux Tribe (YST) living on the YST Reservation in South Dakota.\n\nThe wPap intervention will be tested in a randomized clinical trial (RCT) involving 120 YST women aged 25-65. Participants will be randomly assigned to either: (a) the wPap intervention group (n = 60), receiving personalized, culturally tailored multilevel multimedia messages through a mobile web app along with health navigator support, or (b) a waitlist control group (n = 60), receiving printed educational materials on cervical cancer and screening guidelines along with health navigator support. The intervention will last seven days, with assessments conducted at baseline, one week post-intervention, and six months post-intervention via surveys and telephone follow-up.\n\nThe study tests the following hypotheses:\n\n(H1) women in the wPap intervention group will achieve higher CC screening rates than the waitlist control group; (H2) the wPap group will demonstrate greater improvements in knowledge, attitudes\u002Fbeliefs, self-efficacy, and intention to undergo CC screening; and (H3) the wPap group will report higher satisfaction and acceptance of the intervention compared with the waitlist control group. Findings will inform the feasibility, acceptability, and efficacy of mobile web app interventions tailored to Indigenous communities to improve CC screening.",[29],"Cervical Cancer Screening","NOT_YET_RECRUITING","2026-05-19",{"date":33,"type":34},"2026-05-22","ACTUAL",{"date":36,"type":23},"2026-05",{"date":38,"type":23},"2026-11-15",{"name":40,"class":41},"University of South Dakota","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":17,"sex":49,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":24,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":42},"100576779","mindfulness-based-interventions-targeting-first-generation-college-student-retention-in-rural-environments-100576779","NCT06789731","Mindfulness-Based Interventions Targeting First-Generation College Student Retention in Rural Environments","Inclusion Criteria:\n\n18 years or older. Currently enrolled in four-year college in the United States. First-generation college student. Access to WiFi and a computer\u002Fsmartphone\u002Ftablet. English speaking.\n\nExclusion Criteria:\n\nNot currently enrolled in a four-year college. Not a first-generation college student. Non-English speaker. Not able to utilize WiFi or computer\u002Ftablet\u002Fsmartphone.","ALL","18 Years","64 Years",{"count":53,"type":23},53,[26],"The goal of this randomized control group is to learn about effective treatments for college students experiencing anxiety and\u002For depression. The main questions this clinical trial aims to answer are: 1) Can mindfulness-based treatments increase retention rates among first-generation college students? 1) Can mindfulness-based treatments decrease anxiety and\u002For depression among first-generation college students?\n\nParticipants will be randomly assigned to one of two intervention groups: mindfulness meditation or psychoeducation. Researchers will compare outcomes from each group to explore treatment differences.",[57,58],"Depression","Anxiety","RECRUITING","2026-01-26",{"date":62,"type":34},"2026-01-28",{"date":64,"type":34},"2025-01-01",{"date":66,"type":23},"2027-06",{"name":40,"class":41},{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":17,"sex":49,"minAge":50,"maxAge":51,"enrollmentInfo":74,"targetDuration":4,"studyType":24,"phases":76,"briefSummary":77,"conditions":78,"keywords":80,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":42},"100595341","instructional-influence-how-cueing-alters-foam-rolling-outcomes-100595341","NCT07031193","Instructional Influence: How Cueing Alters Foam Rolling Outcomes","Inclusion Criteria:\n\n* Fluent in English and primary language\n\nExclusion Criteria:\n\n* Current musculoskeletal injury of the lower limbs for which they are receiving medical care.\n* Recent surgery to the lower limbs that has not been fully released for full participation by a medical provider.\n* Use of any pain-relieving medications within the last 24 hours.\n* Any medical condition that limits their perception of pain.",{"count":75,"type":23},52,[26],"Foam rolling (FR) is a common tool and procedure used in rehabilitation. Previous research has demonstrated physical improvements in range of motion and subjective reductions in pain post-intervention. Most of the literature theorizes potential biophysical reasons for these changes, but definitive studies are lacking. Another potential mechanism for these improvements may be psychological.\n\nThe purpose of this study is to explore the psychological changes that occur in response to the instructions given to the patient and how these may influence the outcomes the individual receives while undergoing FR.\n\nDifferent instructions will be given for the same technique of FR to see if there are differences in changes with pain and range of motion.",[79],"Foam Roller",[81,82,83],"foam roller,","range of motion","pain","2025-07-01",{"date":86,"type":34},"2025-07-02",{"date":88,"type":23},"2025-08-01",{"date":90,"type":23},"2026-05-31",{"name":40,"class":41},{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":96,"acronym":4,"eligibilityCriteria":97,"healthyVolunteers":17,"sex":49,"minAge":50,"maxAge":51,"enrollmentInfo":98,"targetDuration":4,"studyType":24,"phases":100,"briefSummary":101,"conditions":102,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":42},"100551846","exercise-induced-hypoalgesia-and-proprioceptive-changes-comparing-isometric-to-isotonic-neck-exercises-100551846","NCT06465394","Exercise-induced Hypoalgesia and Proprioceptive Changes, Comparing Isometric to Isotonic Neck Exercises","Inclusion Criteria:\n\n* 18-64 years old,\n* all genders,\n* healthy individuals with no neck pain\n\nExclusion Criteria:\n\n* Medical restrictions to physical activity\n* History of chronic pain (pain \\> 3 months) or current acute neck pain\n* Unable to refrain from alcohol, pain medications, and vigorous exercise 24 hours prior to testing",{"count":99,"type":23},40,[26],"Exercised induced hypoalgesia (EIH) (reduction in pain) after exercise has been studied in the literature, but no comparisons have been made specifically looking at different types of exercise (isometric\u002Fdynamic moving through a range of motion with resistance versus isotonic\u002Fapplying static resistance to a joint not moving) with neck muscle strengthening. This study will explore to see if one form of exercise is superior to the other in providing EIH.\n\nAnother benefit of exercise is improving proprioception (knowing where our body is in space). Again no specific investigation has been done comparing isometric versus isotonic exercises for neck muscles.\n\nBoth of these exercises are often prescribed in physical therapy so further understanding the benefits of them can help improve the prescription of exercises for patients.",[103],"Exercise","2024-12-03",{"date":106,"type":34},"2024-12-06",{"date":108,"type":34},"2024-08-12",{"date":110,"type":23},"2025-05-05",{"name":40,"class":41},""]