Clinical Trials for Cervical Cancer Screening

Currently registered clinical trials for Cervical Cancer Screening from ClinicalTrials.gov. 16 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Cervical Cancer Screening from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 16
  • Active, not recruiting: 3
  • Completed: 8
  • Other: 23

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT00242723 — Evaluation of Cell Changes in Blood and Tissue in Cancers of the Lung, Esophagus and Lung Lining

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment1559
Study TypeOBSERVATIONAL
ConditionsMalignant Pleural Mesotheliomas NOS; Esophageal Cancers NOS; Lung Cancer NOS; Thoracic Cancers; Cancers of Non Thoracic Origin With Metastases to the Lungs or Pleura

Background:

  • Chromatin is is the structural building block of a chromosome. It is found inside the nucleus of the cell and consists of a complex of DNA and protein.
  • Cancers of the lung, pleura (lung lining) and esophagus show profound changes in chromatin structure that may affect the course of disease in patients.
  • A better understanding of these diseases and the genetic changes associate…

NCT02956031 — Screening Study for Cervical Pre-cancer and Cancer Prevention in South African Women.

StatusRecruiting
PhaseN/A
SponsorUniversity of Pretoria
Enrollment1500
Study TypeOBSERVATIONAL
ConditionsCervical Cancer; High Grade Sil; CIN2
Interventions; ;

Nearly 8 000 new cervical cancer cases are diagnosed in South Africa per year; many are still undiagnosed and about 50% of diagnosed cases succumb per year. Although the current prevalence of pre-cancer cervical disease is largely unknown, data from local studies suggest regional differences and an increase in the prevalence of cytological abnormalities when compared with historical data. Low f…

NCT05334069 — Collecting Blood Samples From Patients With and Without Cancer to Evaluate Tests for Early Cancer Detection

StatusRecruiting
PhaseN/A
SponsorAlliance for Clinical Trials in Oncology
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsAcute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Ann Arbor Stage I Lymphoma; Ann Arbor Stage II Lymphoma; Ann Arbor Stage III Lymphoma
Interventions;

This study collects blood and tissue samples from patients with cancer and without cancer to evaluate tests for early cancer detection. Collecting and storing samples of blood and tissue from patients with and without cancer to study in the laboratory may help researchers develop tests for the early detection of cancers.

NCT05413798 — Urine HPV Testing for Cervical Cancer Screening Among Women Living With HIV in South Africa

StatusRecruiting
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment300
Study TypeINTERVENTIONAL
ConditionsCervical Cancer; CIN2; CIN3
Interventions; ;

The purpose of this study explores the usefulness of urine samples for cervical cancer screening in human immunodeficiency virus (HIV)-infected women.

Cervical cancer occurs when women are infected with the human papillomavirus (HPV), which can cause changes in the cells that lead to cervical precancer and, eventually, cervical cancer if untreated. However, urine HPV testing has not been well …

NCT05092022 — St. Joseph’s HPV Self-sampling: Offering a Self-sampling Option in Clinic

StatusRecruiting
PhaseN/A
SponsorMilton S. Hershey Medical Center
Enrollment50
Study TypeINTERVENTIONAL
ConditionsCervical Cancer Screening
Interventions

This study aims to evaluate the effectiveness of offering self-sampled human papillomavirus (HPV) tests in increasing participation in cervical cancer screening, compared to the standard of care clinician-sampled test. The primary study endpoints are (1) patients’ acceptability of self-sampled HPV tests vs. clinician-sampled test, and (2) patients’ completion of self-sampled HPV test. The secon…

NCT06042543 — Novel, One Stop, Affordable, Point of Care and AI Supported System of Screening, Triage and Treatment Selection for Cervical Cancer in LMICs

StatusRecruiting
PhaseN/A
SponsorInternational Agency for Research on Cancer
Enrollment3200
Study TypeINTERVENTIONAL
ConditionsCervical Cancer; Screening
Interventions

Artificial intelligence (AI) is fast gaining reputation as a highly promising solution for cervical cancer screening. AI-based detection of cervical neoplasias is named automated visual exam (AVE) by the National Cancer Institute, USA. The investigators propose to develop and evaluate the performance characteristics of a novel AI system to both screen and triage women as well as help in treatme…

NCT07224750 — A Noninvasive and Screening miRNA Signature for Gastrointestinal Cancer

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsHepatocellular Carcinoma (HCC); Cholangiocarcinoma; Pancreatic Ductal Adenocarcinoma (PDAC); Esophageal Squamous Cell Carcinoma (ESCC); Gastric Cancer (GC)

Gastrointestinal (GI) cancers remain a major global health burden, largely due to the lack of effective and accessible early screening strategies. Current diagnostic approaches-including endoscopy, computed tomography (CT), and magnetic resonance imaging (MRI)-are either invasive, resource-intensive, or insufficiently sensitive for detecting early-stage disease, and are therefore not suitable f…

NCT07266363 — Integrated Cf-miRNA and Exosomal miRNA Signature for Early Detection of Esophageal Squamous Cell Carcinoma

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment600
Study TypeOBSERVATIONAL
ConditionsESCC
Interventions; ;

Esophageal squamous cell carcinoma (ESCC) remains a highly lethal cancer worldwide, largely due to late diagnosis. Current screening methods such as upper endoscopy are invasive, operator-dependent, and limited in their ability to detect early-stage lesions.

To address this clinical need, the SYNERGY study seeks to develop a non-invasive, blood-based biomarker assay that integrates cell-free m…

NCT06825689 — Unidos Contra el VPH

StatusRecruiting
PhaseN/A
SponsorUniversity of Texas at Austin
Enrollment735
Study TypeINTERVENTIONAL
ConditionsHuman Papilloma Virus (HPV); Cervical Cancers
Interventions; ;

The purpose of the Unidos Contra el VPH study is to help find options to screen, or check, for cervical cancer that individuals can do at home to help prevent and detect cervical cancer early. Usually, people get screened for cervical cancer with a Pap smear and human papillomavirus (HPV) test by a health care provider. This is not always easy for individuals who are not able to get to a clinic…

NCT06843720 — Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems

StatusRecruiting
PhaseN/A
SponsorM.D. Anderson Cancer Center
Enrollment7100
Study TypeINTERVENTIONAL
ConditionsHR-HPV Testing
Interventions

To learn about the attitudes toward implementing self-collection among healthcare providers and staff, participants, and other stakeholders; and to inform the development of patient education and provider training materials to aid in the implementation of self-collection in clinical settings.

NCT06995898 — The Vanguard Study: Testing a New Way to Screen for Cancer

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment24000
Study TypeINTERVENTIONAL
ConditionsBladder Carcinoma; Breast Carcinoma; Colorectal Carcinoma; Esophageal Carcinoma; Gastric Carcinoma
Interventions; ;

The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden o…

NCT06896448 — Innovative OSA Screening in Head and Neck Cancer Patients With the Apneal App

StatusRecruiting
PhaseN/A
SponsorUniversity Hospital, Caen
Enrollment20
Study TypeINTERVENTIONAL
ConditionsObstructive Sleep Apnea Hypopnea Syndrome (OSAHS); Head and Neck Cancers
Interventions

Obstructive sleep apnea syndrome is a common but often underdiagnosed condition, with significant impacts on quality of life, such as fatigue, attention disorders, and an increased risk of heart attack or stroke. Structural changes in the head and neck region appear to contribute to the onset or worsening of this condition.

To improve patients’ quality of life, early diagnosis is essential. Cu…

NCT06800664 — Home-based Self-sampling for Cervical Cancer Prevention Education Intervention in Ghana

StatusRecruiting
PhaseN/A
SponsorBaylor University
Enrollment1500
Study TypeINTERVENTIONAL
ConditionsCervical Cancer Screening; HIV; Self-sampling; Implementation Science; Intervention (Training) Condition
Interventions;

The investigators propose to develop and/or adapt implementation strategies and a structured implementation plan to translate the HOPE intervention into existing healthcare practice in Ghana.

These “implementation support strategies (ISS)” are implementation strategies relevant to implementation support, which is concerned with moving (implementation) research into (implementation) practice.

NCT07428330 — Clinic vs Clinic+Community Outreach HPV Self-Collection to Increase Cervical Screening in Women With HIV

StatusRecruiting
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment7597
Study TypeINTERVENTIONAL
ConditionsCervix Cancer; HIV Infections; HPV Infection
Interventions;

This Clinical Trials Network for Human Immunodeficiency Virus (HIV)-Associated Cervical Cancer Screening and Treatment Optimization (CASCADE) C3001-A trial aims to assess how the introduction of a community-health-worker-facilitated model, in addition to the existing static clinic-only model, influences the rates of cervical cancer screening uptake among women living with HIV (WLWH). This study…

NCT07538050 — Single Visit Clinical Validation of ScreenFire, a Low-Cost HPV Test: Efficacy and Cost Effectiveness (Phase 2)

StatusRecruiting
PhaseN/A
SponsorThe Cleveland Clinic
Enrollment1000
Study TypeINTERVENTIONAL
ConditionsCervical Cancer Screening
Interventions

In high-income countries, prevention strategies have led to declines in cervical cancer rates by more than 75% in high-income countries. In contrast, low- and middle-income countries (LMICs) carry the global burden of cervical cancer with about 85% of new cases and 90% mortality. Screening is an essential component of effective prevention to reduce this disease burden. The World Health Organiza…

NCT07351110 — Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.

StatusRecruiting
PhaseN/A
SponsorUniversity of Florida
Enrollment20
Study TypeINTERVENTIONAL
ConditionsDiabetes; Cervical Cancer (Early Detection); Obesity & Overweight
Interventions

Our overarching goal is to adapt and test the PINPOINT intervention -PatIent Navigation for the Prevention of CervIcal CaNcer inTervention. We will test the PINPOINT intervention among patients with high-risk profiles for cervical cancer who do not meet the recommended screening for cervical cancer.

Active, Not Recruiting

NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment6452
Study TypeINTERVENTIONAL
ConditionsAdvanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma
Interventions; ;

This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…

NCT06002126 — Optimization of Cervical Cancer Screening Among Women Living With HIV in Latin American Countries

StatusActive, not recruiting
PhaseN/A
SponsorWeill Medical College of Cornell University
Enrollment1001
Study TypeINTERVENTIONAL
ConditionsCervix Cancer; HPV Infection; Cervical High Grade Squamous Intraepithelial Lesion; HIV Infections
Interventions;

Cervical cancer is a relatively common cancer among women living with human immunodeficiency virus (HIV). This study will test women for human papillomavirus (HPV) infection of the cervix. The main purpose of this study is to determine the best way to test for damaged areas of the cervix. Damaged areas of the cervix should be treated and removed to prevent cancer of the cervix.

Women living wi…

NCT07581873 — Education and Health in Women With Cervical Cancer

StatusActive, not recruiting
PhaseN/A
SponsorFederal University of Maranhao
Enrollment28
Study TypeINTERVENTIONAL
ConditionsCervical Cancer; Cervical Cancer Screening; Cervical Cancer Prevention
Interventions

Introduction: Cervical neoplasms constitute a significant public health problem on a global scale. According to the National Cancer Institute, this pathology is the third most prevalent type of cancer among women in Brazil, and the second most incident neoplasm in the North and Northeast regions. Estimates for each year of the 2023-2025 triennium point to approximately 17,010 new cases, with a …

Not Yet Recruiting

NCT07574190 — A Mobile Web App Intervention to Promote Cervical Cancer Screening

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of South Dakota
Enrollment120
Study TypeINTERVENTIONAL
ConditionsCervical Cancer Screening
Interventions

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.

The wPap intervention will be tested in a randomiz…

NCT07606677 — Peripheral Blood CyTOF Immune Model for Cervical Lesion Detection in HPV16/18+ Women

StatusNot yet recruiting
PhaseN/A
SponsorWomen’s Hospital School Of Medicine Zhejiang University
Enrollment1465
Study TypeOBSERVATIONAL
ConditionsCIN 2/3; Cervical Cancer (Early Detection)

This prospective, multicenter cohort study will recruit eligible HPV16/18-positive women from three tertiary hospitals in China. Peripheral blood samples and clinical data (cytology, HPV genotyping, colposcopy-directed biopsy) will be collected, followed by standardized mass cytometry (CyTOF) to develop and evaluate an immune model across cervical lesion grades.

NCT07645378 — Feasibility Study Comparing One vs Two Probes for Thermal Ablation Among Cervical Cancer Screen Positive WLWH in C1001P-CS9 South Africa

StatusNot yet recruiting
PhaseN/A
SponsorFred Hutchinson Cancer Center
Enrollment200
Study TypeINTERVENTIONAL
ConditionsHIV (Human Immunodeficiency Virus); HPV; Cervical Precancer; Cervical Neoplasia
Interventions;

Cervical cancer disproportionately affects women in low- and middle-income countries (LMICs), particularly women living with HIV (WLWH) who have a 6-fold increased risk of cervical cancer compared to women in the general population. Thermal ablation (TA) is recommended by the World Health Organization (WHO) to treat cervical precancerous lesions, although its efficacy can be suboptimal in WLWH….

NCT07645352 — Feasibility Study Comparing One vs Two Probes for Thermal Ablation Among Cervical Cancer Screen Positive Women Living With HIV in C1001P-CS7 Zimbabwe

StatusNot yet recruiting
PhaseN/A
SponsorFred Hutchinson Cancer Center
Enrollment300
Study TypeINTERVENTIONAL
ConditionsHIV (Human Immunodeficiency Virus); HPV; Cervical Precancer; Cervical Neoplasia
Interventions;

Cervical cancer disproportionately affects women in low- and middle-income countries (LMICs), particularly women living with HIV (WLWH) who have a 6-fold increased risk of cervical cancer compared to women in the general population. While thermal ablation (TA) is a WHO- recommended treatment for cervical precancerous lesions, its efficacy can be suboptimal in WLWH. We will also conduct a feasib…

NCT07520188 — C-3002: Enhancing Cervical Cancer Screening Access and Follow-up Care at ‘CASCADE’ Clinical Sites in the United States

StatusNot yet recruiting
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment3500
Study TypeOBSERVATIONAL
ConditionsHuman Immunodeficiency Virus (HIV); Human Papillomavirus (HPV); Cervical Cancer; Cervical Precancer
Interventions;

The purpose of the CASCADE-3002 project is to improve access to cervical cancer screening among women with Human Immunodeficiency Virus (HIV) receiving care at U.S.-based CASCADE clinical sites. This study will assess the cervical cancer screening cascade and identify multilevel factors that impede access to screening among women with HIV attending Infectious Disease clinics in Georgia and Mary…

NCT07624123 — Clinic vs Clinic+Community Outreach HPV Self-Collection to Increase Cervical Screening in Women Living With HIV

StatusNot yet recruiting
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment17734
Study TypeINTERVENTIONAL
ConditionsCervix Cancer; HIV Infections; HPV Infection
Interventions;

This Clinical Trials Network for Human Immunodeficiency Virus (HIV)-Associated Cervical Cancer Screening and Treatment Optimization (CASCADE)-3001-B trial aims to assess how the introduction of a community-health-worker-facilitated model, in addition to the existing static clinic-only model, influences the rates of cervical cancer screening uptake among women living with HIV (WLWH). This study …

NCT07644910 — Nudging Preventive Screening Via Message Framing and Bundling

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Chile
Enrollment235000
Study TypeINTERVENTIONAL
ConditionsBreast Neoplasms; Uterine Cervical Neoplasms; Colorectal Neoplasms; Prostatic Neoplasms; Diabetes Mellitus
Interventions; ;

This study is a randomized controlled field experiment embedded in the medical institution Early Diagnosis Program in Chile. Participants with two exams pending (a cancer screening test and a chronic disease test for diabetes and dyslipidemia) will be randomly assigned across a 3 × 3 factorial design: three message framing conditions (Basic, Risk/Importance, Peace of Mind) crossed with three ex…

NCT06872346 — Personalized Risk-based Follow-up of Cervical Cancer Screening in Practice, RCT

StatusNot yet recruiting
PhaseN/A
SponsorMassachusetts General Hospital
Enrollment7500
Study TypeINTERVENTIONAL
ConditionsCervical Cancer Screening
Interventions;

The goal of this PREDICT is to assess a personalize approach to screening and management of cervical cancer testing. The investigators will evaluate patients who are due for a follow up cervical cancer screening in the primary care clinics in the Massachusetts General Brigham system. Patients will be randomized by clinic into three different arms (Arm 1: standard care, Arm 2: visit based remind…

NCT07593066 — PRIORITY Study in Cervical Cancer

StatusNot yet recruiting
PhaseN/A
SponsorPontificia Universidad Catolica de Chile
Enrollment700
Study TypeOBSERVATIONAL
ConditionsCervical Cancer; Cervical Intraepithelial Neoplasia; HPV Infection

The PRIORITY study is a prospective, multicenter observational study designed to evaluate an integrated diagnostic model combining extended molecular self-sampling and digital colposcopy supported by telemedicine for the prioritization of women at risk of cervical cancer.

The study aims to assess the diagnostic performance, concordance, and clinical utility of this integrated approach in real-…

NCT07575217 — Mail-in HPV Screening Program in NJ

StatusNot yet recruiting
PhaseN/A
SponsorRutgers, The State University of New Jersey
Enrollment200
Study TypeINTERVENTIONAL
ConditionsCervical Cancer Screening
Interventions;

The purpose of this study is to help people who have missed their regular cervical cancer screening. The investigators are evaluating whether mailing an HPV self-sampling kit to participant home makes it easier and more convenient for people to get screened for cervical cancer. This study will also help to understand if people find this process acceptable and whether it is an effective way to i…

NCT07294066 — Uniting Trusted Community Messengers to Improve Access to Cervical Cancer Screening in Rural North Carolina

StatusNot yet recruiting
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment112
Study TypeINTERVENTIONAL
ConditionsCervix Cancer; Screen HPV-positive
Interventions

The purpose of this study is to test the feasibility and acceptability of a multi-level, community-engaged intervention to increase access to cervical cancer screening using human papillomavirus (HPV) self-collection (HPVSC) outreach among women living in a high-risk rural county and to improve navigation for follow-up screening.

A one-group intervention evaluation design will be used to pilot…

NCT07657104 — Developing and Implementing HPV SCREENED

StatusNot yet recruiting
PhaseN/A
SponsorRutgers, The State University of New Jersey
Enrollment100
Study TypeINTERVENTIONAL
ConditionsCervical Cancer Screening; Human Papilloma Virus
Interventions

This study will assess the feasibility of implementing HPV self-sampling as a primary cervical cancer screening strategy for under-screened women in the emergency department (ED). Eligible participants will receive education and an HPV self-sampling kit to complete in the ED. Individuals with HPV-positive results will be guided to follow-up care at a local clinic.

NCT06810739 — The Women’s Screening and Self-Testing Program (PROMETA) Study

StatusNot yet recruiting
PhaseN/A
SponsorTulane University
Enrollment8445
Study TypeINTERVENTIONAL
ConditionsHuman Papilloma Virus Related Cervical Carcinoma
Interventions

This proposal directly addresses the ability to safely scale-up a Screen-Triage-Treat approach to cervical cancer screening. The investigators propose to capitalize on a pool of screen-eligible women accessing routine care within targeted human immunodeficiency virus (HIV) care and treatment services. The primary outcome of interest is the number of women screened and the proportion of screen-p…

NCT06708351 — Enhancing Cervical Cancer Screening and Treatment in Women Living With HIV in Kenya, the ENHANCE LINKAge Trial

StatusNot yet recruiting
PhaseN/A
SponsorEmory University
Enrollment2280
Study TypeINTERVENTIONAL
ConditionsHIV Infection; Human Papillomavirus-Related Cervical Carcinoma; Screening Strategy
Interventions; ;

Background In sub-Saharan Africa (SSA), human papillomavirus (HPV) and HIV create a dual burden of disease that causes significant morbidity and mortality in the form of cervical cancer (CC). Women living with HIV (WLWH) have a six-fold higher risk of developing precancerous lesions that persist and progress to CC, which is the leading cause of cancer mortality among women in Kenya. Significant…

NCT07214506 — Human Papillomavirus (HPV) Self-Sampling Options to Promote Equity

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Arizona
Enrollment100
Study TypeINTERVENTIONAL
ConditionsUterine Cervical Neoplasms; HPV Testing; Pap Smear
Interventions;

This study is testing a new way to help people who are unhoused get screened for cervical cancer. Cervical cancer can often be prevented if it is found early. Many people who lack stable housing usually do not receive regular screenings.

Through this project, the investigators will bring screening to community locations in Tucson, Arizona, using a mobile health unit (MHU) from the University o…

NCT06528353 — Blood Biomarkers Based Screening for HPV-driven OPC

StatusNot yet recruiting
PhaseN/A
SponsorUNICANCER
Enrollment10000
Study TypeINTERVENTIONAL
ConditionsHead and Neck Squamous Cell Carcinoma; Anal Cancer; Human Papilloma Virus
Interventions

The objective of our study is to demonstrate that it is possible to detect and treat human papilloma virus (HPV)-related oropharyngeal cancers (OPC) early using simple blood tests. The success of this strategy will be evaluated by the number of participants positive for both HPV16-E6 serology and HPV circulating tumor DNA (ctDNA) whose early management has allowed the detection of a cancerous l…

Enrolling by Invitation

NCT06144229 — Real-world Effectiveness of HPV Vaccine in Women Living With HIV and Its Impact on Cervical Cancer Screening Accuracies

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of California, Los Angeles
Enrollment650
Study TypeOBSERVATIONAL
ConditionsHiv; Hpv
Interventions

This study will examine both Human papillomavirus (HPV) vaccine effectiveness and Primary high-risk HPV PHS screening triage strategies in women living with HIV (WLHIV) by partnering with the Pediatric HIV/AIDs Cohort Study (PHACS) led, in part, by our investigative team. Among WWH, the study will examine the effectiveness of the HPV vaccine The study will screen approximately 810 WWH using a s…

NCT07186530 — Offering HPV Self-Collection in Novel Healthcare Settings to Improve Uptake of Cervical Cancer Screening

StatusEnrolling by invitation
PhaseN/A
SponsorMayo Clinic
Enrollment500
Study TypeINTERVENTIONAL
ConditionsCervical Carcinoma; Human Papillomavirus Infection; Human Papillomavirus-Related Cervical Carcinoma
Interventions; ;

This clinical trial evaluates whether offering human papillomavirus (HPV) self-collection for cervical cancer screening at Mayo Clinic Express Care clinics improves uptake of cervical cancer screening and receipt of appropriate follow-up care. Cervical cancer is preventable through vaccination, screening, and treatment of pre-cancerous conditions. However, cervical cancer screening rates have d…

StatusEnrolling by invitation
PhaseN/A
SponsorThe First Affiliated Hospital of Henan University of Science and Technology
Enrollment12000
Study TypeOBSERVATIONAL
ConditionsEsophageal Cancer
Interventions

The goal of this observational study is to learn about the clinical utility of an artificial intelligence (AI) large language model in patients undergoing screening, diagnosis, treatment, and prognosis assessment for esophageal cancer. The main question it aims to answer is:

Does the AI model improve early detection rate, diagnostic accuracy, treatment personalization, and prognostic predictio…

NCT07682883 — The Importance of Mucosal Screening in the Prevention of Oral Cancer.

StatusEnrolling by invitation
PhaseN/A
SponsorMedical University of Warsaw
Enrollment1383
Study TypeINTERVENTIONAL
ConditionsOPMD; Oral Cancer , Oral Squamous Cell Carcinoma, Oral Cavity Cancer; Oral Potentially Malignant Lesions; Leukoplakia Oral; Oral Mucosa
Interventions;

Patients attending the Department of Oral Mucosal and Periodontal Diseases at the University Dental Center of the Medical University of Warsaw who provide written informed consent will be invited to participate in the study.

Participation will begin with completing a short, anonymous questionnaire. The questions will focus on factors that may increase the risk of developing oral potentially ma…

NCT07592793 — Community Gateway to Health Study

StatusEnrolling by invitation
PhaseN/A
SponsorHarvard School of Public Health (HSPH)
Enrollment100
Study TypeINTERVENTIONAL
ConditionsBreast Cancer Screening; Cervical Cancer Screening; Colon Cancer Screening; Tobacco Cessation
Interventions;

The goal of this study is to evaluate the impact of a multi-level intervention on cancer prevention and social determinants of health outcomes. This partnership between academic and community-based researchers aims to link community health centers and communities in ways that maximize both civic engagement and participation in cancer control care. The system-level intervention consists of two c…

NCT07678047 — Leveraging Project ECHO for Improved Cervical Cancer Screening in Ethiopia

StatusEnrolling by invitation
PhaseN/A
SponsorAlbert Einstein College of Medicine
Enrollment60
Study TypeINTERVENTIONAL
ConditionsCervical Carcinoma; Human Papilloma Virus (HPV)
Interventions

Project TICHILALECH (“she can” in Amharic), a five-year, implementation science study, is focused on improving cervical cancer screening, triage, and treatment and integration with human immunodeficiency virus (HIV) care at five Ethiopian hospitals, with a focus on human papillomavirus (HPV) self-collection as the recommended screening strategy for people living with HIV (PLHIV). To improve imp…

Completed Trials

NCT04927494 — Cervical Cancer Prevention for Black Adults

StatusCompleted
PhaseN/A
SponsorAdebola Adegboyega
Enrollment288
Study TypeINTERVENTIONAL
ConditionsCervical Cancer
Interventions

The goal of this study is to develop and pilot test an intervention, entitled Health is Wealth: A Cervical Health Program, designed to promote screening and reduce perceived barriers to Cervical Cancer (CC) screening.

Aim 1: Examine general awareness and cultural factors (fatalism, religiosity/spirituality, temporal orientation, medical mistrust, and acculturation) related to cancer control an…

NCT06106165 — Improving Muslim Women’s Uptake of Cancer Screening (IMCAN)

StatusCompleted
PhaseN/A
SponsorUniversity of Sunderland
Enrollment169
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; Bowel Cancer; Cervical Cancer
Interventions;

The goal of this non-randomised trial is to test how a workshop that includes religiously-tailored messages can help increase the uptake of breast, colorectal and cervical cancer screening among Muslim women in North East England and Scotland.

The results of this trial will inform the development of a full-scale randomised-controlled trial.

Participants in this study will be asked to take par…

NCT06259448 — Feasibility of Optimizing Organized Cervical Cancer Screening by Urine Self-sampling

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Bordeaux
Enrollment173
Study TypeINTERVENTIONAL
ConditionsCervical Cancer
Interventions

This project addresses the issue of promoting organized cervical cancer screening (CCS) from the perspective of the use of urine self-sampling (USS). Via a prospective and monocentric study, the present study aims to evaluate the acceptability of women to collect a urine self-sample and to respond to a questionnaire on their feelings about this screening method.

NCT06302725 — Vaginal Self-sampling for Detecting High-risk Human Papillomavirus Cervical Infection in Patients With Immune-mediated Inflammatory Diseases

StatusCompleted
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment278
Study TypeINTERVENTIONAL
ConditionsHPV Infection; Systemic Disease
Interventions

Main objective: -To determine Human Papilloma Virus (HPV) prevalence in patients with immune-mediated inflammatory diseases (IMID) using vaginal self-sampling (VSS), one year after VSS was proposed Primary endpoint: - To determine the prevalence of HPV infection (yes/no) after VSS proposal Secondary objectives: - To describe the HPV typology and the rate of co-infection (with several high-risk …

NCT06647992 — Effect of Nurse Navigation Program on Cervical Cancer Screening Behaviour of the Women Aged 30-65

StatusCompleted
PhaseN/A
SponsorTURKAN OZDAS
Enrollment80
Study TypeINTERVENTIONAL
ConditionsCervical Cancers
Interventions

This study was designed as a randomized controlled experimental study to examine the effect of the ‘Nurse Navigation Program’ on cervical cancer screening behaviors (Human Papilloma Virus (HPV) DNA screening test and/or pap smear test) and health beliefs about cervical cancer screening in women aged 30-65 years.

NCT06874985 — Effectiveness and Impact of the Lived Experience Cancer Awareness Campaign on Screening Participation

StatusCompleted
PhaseN/A
SponsorInternational Agency for Research on Cancer
Enrollment1264
Study TypeINTERVENTIONAL
ConditionsCervical Cancers; Breast Cancer; Oral Cancer
Interventions

This study will be conducted as a parallel-arm, open-label, randomized controlled trial (RCT) to evaluate the effectiveness and impact of the Lived Experience Communication Campaign (LECC) on cancer screening participation rates [oral, breast and cervical cancer] compared to the usual standard awareness campaign across selected rural population in Villupuram district, Tamil Nadu.

NCT07017387 — Impact of Education Methods on HPV Knowledge and Screening Behavior

StatusCompleted
PhaseN/A
SponsorSaglik Bilimleri Universitesi Gulhane Tip Fakultesi
Enrollment90
Study TypeINTERVENTIONAL
ConditionsHealth Education; Motivational Interviewing
Interventions;

The aim of this study is to evaluate the effect of two different health education methods (one based on motivational interviewing) on women’s HPV knowledge, cervical cancer health beliefs, and screening behaviors in women aged 30-65. A total of 90 healthy women who are registered at the Incirli Family Health Center in Ankara, meet the inclusion criteria, and volunteer to participate will be ran…

NCT07451340 — Cross-Cultural Adaptation and Psychometric Validation of the Cervical Cancer Screening Uptake Questionnaire (CCSTQ) in Turkish Women

StatusCompleted
PhaseN/A
SponsorAnkara University
Enrollment530
Study TypeOBSERVATIONAL
ConditionsHealthy; Cervical Cancer Screening
Interventions

Cervical cancer remains an important public health issue affecting women’s health. Cervical cancer screening plays a key role in reducing morbidity and mortality through early detection. Women’s decisions to participate in screening are influenced not only by knowledge, but also by psychosocial factors such as social norms, perceived threat, perceived benefits and barriers, and self-efficacy. T…

Other (Terminated)

NCT03598946 — Urinary Human Papilloma Virus Test in the General Population in Brittany

StatusTerminated
PhaseN/A
SponsorUniversity Hospital, Brest
Enrollment1809
Study TypeINTERVENTIONAL
ConditionsNeoplasms,Ovarian
Interventions

This is a population-based, prospective, multicenter and open-label study. 12,500 female non-respondents to the uterine cervix smear from 30 to 65 years of age in the context of the organized cervical cancer screening of the uterus, in the 4 Breton departments, will be proposed after stratification by age and socio-economic level at the revival of the cervical cancer of the uterus screening by …