Clinical Trials Logo

Uterine Cervical Neoplasms clinical trials

View clinical trials related to Uterine Cervical Neoplasms.

Filter by:
  • Completed  
  • Page 1 ·  Next »

NCT ID: NCT06440382 Completed - Cervical Cancer Clinical Trials

Scottish Cervical Screening and Ethnicity Project

SCREEN
Start date: March 1, 2019
Phase:
Study type: Observational

To identify important ethnic inequalities in cervical cancer screening participation in Scotland, and explore possible reasons for these.

NCT ID: NCT06365450 Completed - Breast Cancer Clinical Trials

Breast and Cervical Cancer Education Program

OCEAP
Start date: September 22, 2022
Phase: N/A
Study type: Interventional

The primary goal of this study is to improve cancer literacy in Black women living with HIV and ultimately improve breast and cervical cancer screening uptake. This study involves an educational intervention delivered virtually and in person, depending on the participants' preference.

NCT ID: NCT06226350 Completed - Cervical Cancer Clinical Trials

A Phase Ⅱ Study of F520 in Patients With Cervical Carcinoma

Start date: March 4, 2021
Phase: Phase 2
Study type: Interventional

This study was an open, single-arm, enriched, multicenter Phase II study.

NCT ID: NCT06177236 Completed - Cervical Cancer Clinical Trials

Clinic or Self-Sampling for Cervical Cancer Screening

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

Objective: The aim of this project was to determine the effect of clinic or self-sampling on attendance, attitudes, and anxiety in cervical cancer screening.

NCT ID: NCT06082505 Completed - Breast Cancer Clinical Trials

Salud en Mis Manos - Breast and Cervical Cancer Prevention and Early Detection - Expansion 1

SEMM1
Start date: November 1, 2016
Phase: N/A
Study type: Interventional

The purpose is to evaluate implementation of a community-based prevention project aimed at increasing early detection and prevention of breast and cervical cancer through education and navigation and to increase breast and cervical cancer screening and Human Papillomavirus (HPV) vaccination in underserved Latinas.

NCT ID: NCT06032481 Completed - Cervical Cancer Clinical Trials

System to Evaluate the Risk of Lymph Node Metastasis Preoperatively in Cervical Cancer

Start date: January 1, 2012
Phase:
Study type: Observational

The lymph node status is difficult to be assessed preoperatively, this study aimed to develop a scoring system for predicting the risk of LNM in cervical cancer patients before operation.

NCT ID: NCT06021496 Completed - Clinical trials for Early Detection of Cancer

The Effect of Face-to-face and Online Health Education on Women's Cervical Cancer Knowledge, Health Beliefs and Screening

Start date: February 14, 2023
Phase: N/A
Study type: Interventional

Aim: The aim of this study is to determine the effect of health education given by two different methods on women's knowledge about HPV, cervical cancer health belief and screening test. Materials and Methods: The study was conducted in a parallel groups design as a single-blind randomized controlled trial. The sample consisted of 126 healthy participants, 42 in each volunteer group, who were registered at the Martyr Zafer Çalışkan Family Health Center in Ankara between January and July 2023, and met the inclusion criteria. HPV Knowledge scale, Cervical Cancer and pap Smear Test Health Belief Model Scale and VAS for self-assessment were used in the study. In the study, while the control group received standard care, the face-to-face education group was given health education and brochures through home visits and a reminder interview over the phone; On the other hand, the online training group was given health education and a digital brochure via video call and a reminder meeting was held once. One-way analysis of variance and Kruskal Wallis test were used to compare the data of the three groups after a two-month follow-up, Tukey and Dunn test for multiple comparisons, and Wilcoxon test for in-group comparisons before and after. In addition, two-way analysis of variance and Robust ANOVA were used in group and time comparisons.

NCT ID: NCT05996796 Completed - Cervical Cancer Clinical Trials

Dry Run of the ScreenUrSelf Trial

Start date: April 10, 2023
Phase: N/A
Study type: Interventional

The proposed study is the Dry Run preceding the ScreenUrSelf trial.

NCT ID: NCT05907187 Completed - Cervical Cancer Clinical Trials

Research in Ethno-Medicine and Education (REMED)

REMED
Start date: November 7, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to gain information about intravaginal practices, like intravaginal "twalet deba", among Haitian women living in South Florida. Intravaginal "twalet deba" may include douching, cleaning inside the vagina with different kinds of products, or using steam/vapor that enter the vagina. The investigators want to help learn the best way to increase early detection and/or prevention for cervical cancer. The investigators would like to know what plants, herbs, commercial products and medicines are used in these practices, how these products are prepared, applied, why these products are used, and how these products affect the vagina and cervix.

NCT ID: NCT05862844 Completed - Cervical Cancer Clinical Trials

Promise Women Project

Start date: September 25, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to develop and test an intervention program to improve cervical cancer prevention among Muslim American women. The main questions the investigators aim to answer are: - Will the religiously tailored and culturally appropriate intervention program improve participants' knowledge and acceptance of cervical cancer prevention? - Is the intervention program feasible to conduct and acceptable to participants? Participants will be asked to: - Attend focus group sessions to provide input on the development of educational materials. - Complete pre- and post-intervention surveys to measure changes in knowledge and acceptance of cervical cancer prevention. - Engage in the intervention program, which includes education and experiential practice/communication skills training. - Provide feedback through satisfaction surveys. Researchers will compare participant outcomes before and after the intervention to assess its effectiveness. Additionally, the program's feasibility and acceptability will be evaluated based on enrollment rates, successful implementation, participant engagement, retention, and satisfaction.