Status:
UNKNOWN
Patient-reported Outcome Measures (PROMs) in Patients With Bodily Stress Syndrome: Protocol for a Prospective Cohort Study
Lead Sponsor:
Helsinki University Central Hospital
Conditions:
Fibromyalgia
Irritable Bowel Syndrome
Eligibility:
All Genders
18-80 years
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 Univer...
Eligibility Criteria
Inclusion
- All genders
- Age 18-80 years
- Referred to Clinic for Functional Disorders either from other hospital units or from primary care
- Willingness to be enrolled in the study, by signing the informed consent
Exclusion
- Patients not able to fill in the forms in Finnish or due to physical constraints (e.g. dystonia)
- Symptoms are likely due to a somatic disorder
Key Trial Info
Start Date :
March 9 2020
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2023
Estimated Enrollment :
400 Patients enrolled
Trial Details
Trial ID
NCT04667611
Start Date
March 9 2020
End Date
December 1 2023
Last Update
December 16 2020
Active Locations (1)
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1
Clinic for Functional Disorders, Helsinki University Hospital
Helsinki, Finland, 00009