Viewing Study NCT06177236



Ignite Creation Date: 2024-05-06 @ 7:53 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06177236
Status: COMPLETED
Last Update Posted: 2023-12-20
First Post: 2023-11-22

Brief Title: Clinic or Self-Sampling for Cervical Cancer Screening
Sponsor: Istanbul University - Cerrahpasa IUC
Organization: Istanbul University - Cerrahpasa IUC

Study Overview

Official Title: The Effect of in Clinic or Self- Sampling for Cervical Cancer Screening on Status of Particitipation Attitude and Anxiety
Status: COMPLETED
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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
Detailed Description: Introduction Persistent infection with high-risk HPV strains is the main cause of cervical cancer

Objective The aim of this study was to determine the effect of clinic or self-sampling on cervical cancer screening participation attitudes and anxiety in women

Method The study was conducted as a descriptive and randomized controlled study between October 2022 and December 2023 in Ödemiş ASM No 2 Ministry of Health Republic of Turkey The first phase of the study was conducted with 309 women and the Introductory Information Form and Attitude Scale for Early Diagnosis of Cervical Cancer were used to evaluate participation and attitudes towards cervical cancer screening The second phase of the study was conducted as a randomized controlled trial with 110 women in the experimental n55 and control n55 groups The women in the experimental group were trained before the procedure and were allowed to take samples from the vaginal area on their own The women in the control group were sampled from the cervical region by the clinician Both groups were pretested before the procedure using the Descriptive Information Form and the State Anxiety Inventory to measure anxiety After the sampling procedure the post-test was administered to the experimental and control groups using the State Anxiety Inventory

Results According to the screening method preferences of the women 34 n105 preferred a self-test 184 n57 preferred a test performed by a clinician in a clinic 39 n12 preferred no method and 437 n135 preferred both methods In the study it was found that the self-test option increased participation in screening The mean total score of the women was found to be 1028965660 This result shows that women have high positive attitudes towards early diagnosis of cervical cancer In the second stage of the study it was observed that the descriptive characteristics of the experimental and control groups showed homogeneous distribution While there was no significant difference between the experimental and control groups in terms of anxiety level in the pretest it was found that the control group had a significantly higher anxiety level in the posttest

Conclusion In this study it was observed that women had positive attitudes towards cervical cancer screening self-sampling increased participation in screening and decreased anxiety levels

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None