Viewing Study NCT06401850



Ignite Creation Date: 2024-05-11 @ 8:30 AM
Last Modification Date: 2024-10-26 @ 3:28 PM
Study NCT ID: NCT06401850
Status: RECRUITING
Last Update Posted: 2024-05-21
First Post: 2024-05-02

Brief Title: Polycystic Ovary Syndrome and Education
Sponsor: Marmara University
Organization: Marmara University

Study Overview

Official Title: Training Given to Women With Polycystic Ovary Syndrome Effect on Quality of Life A Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-05
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: Aim This research is being designed to determine the effect of Polycystic Ovary Syndrome PCOS education given to women on their quality of life In this context the aim of the project is The aim is to determine the impact of the education given to women with PCOS on the quality of life of the training given to women with the disease such as psychosocial and emotional status fertility sexual function obesity and menstrual irregularity and hair growth

Method Within the scope of this research quantitative research method is used as the research method In addition it is planned as a randomized controlled quasi-experimental which is one of the quantitative research methods In calculating the sample size type 1 error research power and effect size parameters are determined before the research begins Studies generally need to have at least 80 power In order to find a significant difference it is calculated that there should be at least 30 students in each group at 80 power and 95 confidence level Considering the possible risks it is planned to include 70 women in total in 2 groups study and control with 35 women in each group All individuals who want to respond to the survey are included in the sample The process of finding a subject continues until the desired size is reached In addition during the data collection process participants were asked They are asked whether they are diagnosed with PCOS and those who answer yes are included in the sample Within the scope of the research the voluntariness of the participants is essential and both written and verbal consents are obtained from each participant through an informed consent form Personal Information Form and Polycystic Ovary Syndrome Quality of Life-50 Scale created by the researchers were used as data collection tools
Detailed Description: None

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