MedTrace Logo

Patient-reported Outcome Measures (PROMs) in Patients With Bodily Stress Syndrome: Protocol for a Prospective Cohort Study

NCT04667611 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2020-12-16

No results posted yet for this study

Summary

This cohort study implements patient reported outcome measures (PROMs) for patients with bodily stress syndrome in a clinic for functional disorders.

Conditions

  • Fibromyalgia
  • Irritable Bowel Syndrome
  • Somatic Symptom
  • Chronic Fatigue Syndrome
  • Fatigue
  • Dysphagia
  • Exhaustion; Syndrome

Interventions

BEHAVIORAL

Psychosocial interventions

Cognitive behavioural therapy (CBT) based individual and group intervention

Sponsors & Collaborators

  • Helsinki University Central Hospital

    lead OTHER

Principal Investigators

  • Helena Liira, MD, PhD · Helsinki University Central Hospital

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-03-09
Primary Completion
2022-12-31
Completion
2023-12-31

Countries

  • Finland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04667611 on ClinicalTrials.gov