Ignite Creation Date:
2024-05-06 @ 3:32 PM
Last Modification Date:
2024-10-26 @ 1:51 PM
Study NCT ID:
NCT04667611
Status:
UNKNOWN
Last Update Posted:
2020-12-16
First Post:
2020-12-08
Brief Title:
Patient-reported Outcome Measures PROMs in Patients With Bodily Stress Syndrome Protocol for a Prospective Cohort Study
Sponsor:
Helsinki University Central Hospital
Organization:
Helsinki University Central Hospital
Study Overview
Official Title:
Patient-reported Outcome Measures PROMs as Characteristics and Prognostic Factors in Patients With Bodily Stress Syndrome Protocol for a Prospective Cohort Study
Status:
UNKNOWN
Status Verified Date:
2020-12
Last Known Status:
RECRUITING
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:
SYMPA
Brief Summary:
This cohort study implements patient reported outcome measures PROMs for patients with bodily stress syndrome in a clinic for functional disorders
Detailed Description:
The Sympa Cohort study is a prospective single site cohort study that consists of administration of PROMs questionnaires to patients that attend the Clinic for Functional Disorders at Helsinki University hospital HUS The questionnaires are handed out to the study population within seven days before their first visit at the clinic and then at the following 3 6 and 12 months The study population consists of consecutive adult patients that are referred to the clinic either from other hospital units or primary care The collected data will later be linked with national registries on diagnoses medication use and work ability The Sympa Cohort study may have implications in targeting the factors influencing functional outcomes and quality of life reported by patients with bodily stress syndrome It will also form a quality register for the Clinic and characterize the first systematic collection of PROMs related to these disorders in Finland
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