[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100647075":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":20,"locations":25,"responsibleParty":45,"collaborators":20,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":49,"sex":55,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":20,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":67,"overallStatus":72,"whyStopped":20,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":82},{"fullName":5,"class":6},"Texas Tech University Health Sciences Center","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"RISE-W Intervention","EXPERIMENTAL","Participants receive the 12-week RISE-W micro-movement prevention program: brief bouts of light-to-moderate movement each waking hour (target ≥10 hours\u002Fday), supported by a wearable activity tracker that provides hourly movement reminders and enables self-monitoring.",[13],"Behavioral: RISE-W Micro-Movement Program",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","RISE-W Micro-Movement Program","Brief, frequent bouts of light-to-moderate movement performed each waking hour (target ≥10 hours\u002Fday) over 12 weeks, supported by a Fitbit Inspire 3 activity tracker that delivers automated hourly movement reminders and enables self-monitoring.",[9],null,[22],{"name":23,"affiliation":5,"role":24},"Jeni Page, PhD, APRN, ACNP-BC","PRINCIPAL_INVESTIGATOR",[26],{"facility":27,"status":20,"city":28,"state":29,"zip":30,"country":31,"countryCode":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"Texas Tech University Health Sciences Center Clinical Research Institute","Lubbock","Texas","79430","United States","US",{"type":34,"coordinates":35},"Point",[36,37],-101.85517,33.57786,{"lat":37,"lon":36},[40],{"name":41,"role":42,"phone":43,"phoneExt":20,"email":44},"CRI Research Assistant","CONTACT","806-743-4222","clinicalresearch@ttuhsc.edu",{"type":46,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100647075","fitbit-tracked-micromovement-for-cardiometabolic-health-in-rural-women-100647075",false,"NCT07704749","Fitbit-Tracked Micromovement for Cardiometabolic Health in Rural Women","Rural Initiative for Inflammatory Screening & Engagement for Women","RISE-W","Inclusion Criteria:\n\nFemale, aged 18 to 80 years Physically inactive, defined as less than 150 minutes of moderate-intensity physical activity per week (by self-report) Metabolic syndrome, defined as three or more cardiometabolic risk factors consistent with NCEP ATP III criteria, based on documented diagnosis or clinical history: waist circumference \\>88 cm; blood pressure ≥130\u002F85 mmHg; fasting blood glucose ≥100 mg\u002FdL; triglycerides ≥150 mg\u002FdL; HDL cholesterol \\\u003C50 mg\u002FdL Access to a personal or household smartphone (Apple iOS 16.4 or higher, or Android OS 11.0 or higher) capable of installing the Fitbit application; no cellular data plan required Working email address Able to understand and provide written informed consent in English or Spanish Receiving care at one of the three Larry Combest Community Health \\& Wellness Center sites\n\nExclusion Criteria:\n\nCurrent pregnancy or planning to become pregnant during the study period Medical conditions that preclude safe participation in light-to-moderate physical activity (e.g., unstable cardiovascular disease, uncontrolled hypertension, severe musculoskeletal limitations), as determined by the PI through EHR review Participation in another structured lifestyle or cardiometabolic intervention study within the past 6 months (self-report) Use of medications or treatments that significantly alter inflammation or metabolism (e.g., systemic corticosteroids, recent chemotherapy), as determined by the PI through EHR review Inability to comply with study procedures, including wearing the activity tracker or completing follow-up assessments No access to a smartphone, or a smartphone unable to run the Fitbit application due to operating system incompatibility","FEMALE","18 Years","80 Years",{"count":59,"type":60},125,"ESTIMATED","INTERVENTIONAL",[63],"NA","This pilot study tests whether a low-burden prevention program can be integrated into routine care to identify and reduce cardiometabolic risk in rural women. Rural women face high rates of cardiometabolic syndrome, a cluster of conditions (elevated blood pressure, abdominal obesity, abnormal cholesterol, and high blood sugar) that raises the risk of heart disease and diabetes, yet often face barriers to prevention and screening.\n\nThe study enrolls physically inactive adult women with multiple cardiometabolic risk factors who receive care at a rural federally qualified health center. At a baseline visit, participants complete surveys and clinical assessments including inflammatory biomarkers (C-reactive protein and interleukin-6), metabolic labs, blood pressure, waist circumference, menopausal status, and social determinants of health. Participants then take part in a 12-week program of brief, frequent daily movement supported by a wearable activity tracker. Assessments are repeated at 12 weeks.\n\nBecause this is a single-group pilot, every participant receives the program and serves as her own comparison. The study evaluates whether the model is feasible to run within routine clinic workflows and examines preliminary changes in cardiometabolic and inflammatory risk indicators. Findings will inform larger studies of scalable prevention strategies for rural women.",[66],"Cardiometabolic Risk Factors",[68,69,70,71],"micro-movement","cardiometabolic syndrome","rural","women","NOT_YET_RECRUITING","2026-07-10",{"date":75,"type":76},"2026-07-15","ACTUAL",{"date":78,"type":60},"2026-09",{"date":80,"type":60},"2027-05",{"name":5,"class":6},1]