Ignite Creation Date:
2024-05-06 @ 6:45 PM
Last Modification Date:
2024-10-26 @ 2:54 PM
Study NCT ID:
NCT05771532
Status:
COMPLETED
Last Update Posted:
2023-03-16
First Post:
2023-03-05
Brief Title:
A Prospective and Randomized Controlled Evaluation of Sexual Health Education Program of Gynecological Cancer Women
Sponsor:
Chang Gung Memorial Hospital
Organization:
Chang Gung Memorial Hospital
Study Overview
Official Title:
Evaluation of a Gender-sensitive Sexual Health Education Program for Women With Gynecologic Cancer A Prospective and Randomized Controlled Evaluation of Sexual Health Education Program of Cervical Cancer Women
Status:
COMPLETED
Status Verified Date:
2023-02
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:
The purpose of this study was to evaluate the effectiveness of the Gender-Sensitive -Sexual Health Education Program GS-SHEP in enhancing the sexual health of patients with gynecologic cancer
Detailed Description:
This study recruited patients with cervical cancer from the gynecological wards of a large-scale medical center in northern Taiwan A total of 63 participants were divided into two groups The control group n30 received routine sexual health teaching a 10-15-minute routine individual sexual health education and a sexual health pamphlet without a gender-sensitive and theoretically based design The experimental group n33 received the GS-SHEP a 10-15-minute individual sexual health education and a sexual health pamphlet GS-SHEP effectiveness was examined using a self-report instrument to measure background information and three dependent variables sexual knowledge sexual attitudes sexual self-efficacy and sexual activity Data were collected at baseline one week six weeks four months and seven months after intervention and analyzed using the statistical software SPSS 200
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