Viewing Study NCT06357793



Ignite Creation Date: 2024-05-06 @ 8:22 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06357793
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-30
First Post: 2024-04-05

Brief Title: Evaluation of Work Productivity and Activities of the Fibromyalgia Patients Relatives
Sponsor: Başakşehir Çam Sakura City Hospital
Organization: Başakşehir Çam Sakura City Hospital

Study Overview

Official Title: Evaluation of Work Productivity and Activities of the Relative Living With a Patient With Fibromyalgia Syndrome
Status: NOT_YET_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: Patients suffering from fibromyalgia FM are challenged by symptoms such as chronic pain fatigue sleep disturbance and emotional distress Patients diagnosed with fibromyalgia can also negatively affect the relatives they live with due to their existing complaints It is possible that their relatives accompanying them may lose their workforce due to untreated pain complaints and frequent hospital admissions The main purpose of our study is to examine whether there is any impact on the working life of the people they live with and whether there is a decrease in their work productivity
Detailed Description: This cross-sectional study will evaluate FM patients and their relatives who are in paid full- or part time employment at the time of the assessment The study protocol doesnt require any medical intervention Fibromyalgia severity will be assessed with the fibromyalgia impact questionnaire FIQ Evaluation of patient relatives work productivity and activities will be made with the Work Productivity and Activity Impairment questionnaire General Health WPAIGH Analyzes will be completed with a group of healthy controls in the study

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