[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cancer-cervix\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cancer-cervix":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,44,69],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100599941","building-connections-100599941",false,"NCT07091032","Building Connections","Building Connections Between Practices, Patients, and Community Health","Inclusion Criteria:\n\n* The general inclusion criteria involve being 18+, speaking English or Spanish, and meeting one or more of the following criteria:\n\nObesity: Patients with a body mass index of 30 kg\u002Fm2 or greater (i.e., obese category).\n\nCancer screening: Average-risk patients without recommended colorectal or cervical cancer screenings for their age group and biological sex. Specifically:\n\nColon Cancer (CRC) inclusion criteria: Patients aged 45-75 who are due for screenings, with last FIT longer than 1 year ago, last colonoscopy longer than 10 years ago, and last Cologuard longer than 3 years ago.\n\nAnd\u002For\n\nCervical cancer inclusion criteria: Women and patients with a cervix aged 30-65 who are due for screening: with last pap longer than 3 years ago; last co-test longer than 5 years ago; last primary HPV screening longer than 5 years ago.\n\nMental health: Patients with moderate to severe depression or anxiety symptoms.\n\nExclusion Criteria:\n\n* The general exclusion criteria are: those with current pregnancy, or the participant is cognitively impaired, not having a visit to the primary care clinic in the prior 2 years, and speaking a language other than English or Spanish.\n\nExclusion criteria for obesity intervention: had prior metabolic or bariatric surgery or planning to have this surgery in the next 6 months, currently enrolled in an intensive lifestyle program.\n\nExclusion criteria for cancer screening intervention include:\n\nColon Cancer (CRC) exclusion criteria: has colorectal cancer documented in the problem list; has ulcerative colitis or Crohn's disease documented in the problem list\n\nCervical cancer exclusion criteria: has cervical cancer documented in the problem list; has had a prior hysterectomy.\n\nExclusion criteria for mental health: include patients with active suicidality, active substance use disorder, a history of schizophrenia or bipolar disorder, or who are already receiving behavioral health care (therapy sessions in the past 3 months or an appointment upcoming in the next month).","ALL","18 Years","75 Years",{"count":20,"type":21},3600,"ESTIMATED","INTERVENTIONAL",[24],"NA","Building Connections seeks to address health and healthcare inequities in socially vulnerable communities. The project will be conducted in collaboration with clinical practices across Massachusetts, serving a diverse population heavily represented in Community Clinics and Health Centers. The program will offer evidence-based interventions in obesity\u002Fweight management, cancer screening, and mental health.",[27,28,29,30],"Cancer Colorectal","Cancer Cervix","Depression, Anxiety","Obesity","RECRUITING","2025-11-17",{"date":34,"type":35},"2025-11-18","ACTUAL",{"date":37,"type":35},"2025-08-07",{"date":39,"type":21},"2029-12-30",{"name":41,"class":42},"Massachusetts General Hospital","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":51,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":43},"100567860","role-of-colposcopy-in-evaluation-of-suspicious-cervix-100567860","NCT06673680","Role Of Colposcopy In Evaluation Of Suspicious Cervix","Inclusion Criteria:\n\n* Age from 30 to 64 years old.\n* Women with symptoms such as white discharge, post-coital bleeding, and intermenstrual bleeding.\n* Women with the clinically unhealthy cervix (erosion, bleeding on touch, simple leukoplakia, keratinization)\n* Women with Pap smear showing dysplasia\n\nExclusion Criteria:\n\n* Pregnant women\n* Women having active vaginal bleeding.\n* Any past treatment for cervical lesions.\n* Women having frank growth of cervix.\n* Women who underwent a hysterectomy.",true,"FEMALE","60 Years",{"count":54,"type":21},53,"OBSERVATIONAL","do colposcopy and cervical punch biopsy then compare between findings",[28],[59],"screening in cancer cervix","2024-11-01",{"date":62,"type":35},"2024-11-05",{"date":64,"type":35},"2024-10-01",{"date":66,"type":21},"2025-05-30",{"name":68,"class":42},"Sohag University",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":75,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":77,"conditions":78,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":90},"100489434","archery---artificial-intelligence-based-radiotherapy-treatment-planning-for-cervical-head-and-neck-and-prostate-cancer-100489434","NCT05653063","ARCHERY - Artificial Intelligence Based Radiotherapy Treatment Planning for Cervical, Head and Neck and Prostate Cancer","Inclusion Criteria:\n\n1. Consecutive patients with histologically confirmed head and neck cancers of the oropharynx, larynx, hypopharynx and nasopharynx (Stage I-III) that have given consent for radical radiotherapy.\n2. Consecutive histologically confirmed primary cervical cancer patients (Stage IB-IIIB including pelvic node positive) that have given consent for radical radiotherapy.\n3. Consecutive histologically confirmed primary prostate cancer patients (T1-4N0M0) that have given consent for radical radiotherapy.\n4. Mental capacity to understand and consent to participate in the study.\n5. Patients aged ≥18years.\n\nExclusion Criteria:\n\n1. Patients requiring radiotherapy after curative surgery or surgery that is intended to remove as much of the tumour as possible.\n2. Patients receiving palliative radiotherapy\n3. Patients aged \\\u003C 18years.",{"count":76,"type":21},990,"The aim of this study is to look at whether an Artificial Intelligence (AI) based computer program can automate two components of the radiotherapy treatment pathway to a sufficient quality standard to enable its routine clinical use. The two components include the delineation (outlining) of anatomical areas that are at risk of tumour spread and at risk of radiation damage, and the definition of the position, size and shape of the radiation beams.\n\nThe AI-based computer programs have been developed to perform tasks that would normally require direct human involvement by oncologists and medical physicists. Proposed advantages include improved treatment accuracy, as well as a reduction in the time (from weeks to minutes) and human resources needed to deliver radiotherapy, which this study will test.",[79,80,28],"Cancer of Prostate","Cancer Head Neck","2024-05-20",{"date":83,"type":35},"2024-05-22",{"date":85,"type":35},"2023-12-07",{"date":87,"type":21},"2026-09-01",{"name":89,"class":42},"University College, London",6]