NOTES: The Norwegian Tick Born Encephalitis Study

Sponsor
Sykehuset Telemark (Other)
Overall Status
Recruiting
CT.gov ID
NCT05138055
Collaborator
Sykehuset i Vestfold HF (Other), Norwegian Institute of Public Health (Other), Sorlandet Hospital HF (Other), Oslo University Hospital (Other)
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Study Details

Study Description

Brief Summary

During 2018, 2019, and 2020, the reported TBE-cases have increased markedly in Norway. Surveillance studies conducted by the Norwegian Institute of Public Health demonstrate that cases are associated with tick bites in the coastal areas of the Agder, Buskerud, and Vestfold and Telemark counties There is a urgent need for more knowledge of the consequences of TBE in Norway, in particular the identification of patients at risk of long-term sequela. Hence, the overall objective of this project is to gain more knowledge about the natural course of TBE in Norway, and its impact on long-term health-related quality of life and associated factors. Clinical data, biological sampling and PROMs are collected from TBE-infected patients admitted to three hospitals within the epidemic region in Norway.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Detailed Description

This project is designed as a multicenter study divided into four sub-studies:

Substudy 1: A retrospective descriptive study of the clinical features and objective findings of the acute phase of the TBE-patients diagnosed with TBE in South-East Norway during 2018, 2019 and 2020.

Substudy 2: A prospective multicenter study of health related QOL one year after hospitalization with TBE in South-East Norway from 2019 - 2023. The self-reported health-related QOL (assesedby SF-36) of the TBE-patients will be compared with the SF-36 reference values in the Norwegian population.

Substudy 3: A prospective multicenter study of self-reported cognitive function one year after hospitalization with TBE in South-East Norway from 2019- 2023. The cognitive function, measured by PROMS, will be compared with PROMS from an included reference group from the patient's social environment.

Substudy 4: Analyses of biological samples collected at baseline, 3 months and 12 months after hospitalization for TBE in patients included in substudy 2 and 3. These analyses will be conducted to gain more knowledge of the pathogenesis of TBE infection and in particular, which molecular pathways and biomarkers that characterize the TBE infected patients who are hospitalized in Norway. Analyses to identify associations between the acute inflammatory response and long-term outcome will be performed.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
The Norwegian Tick Born Encephalitis Study Acute Phase Characteristics and Long-tern Outcomes
Actual Study Start Date :
Oct 1, 2020
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Outcome Measures

Primary Outcome Measures

  1. To describe the acute phase clinical and immunological characteristics of TBE in Norway [4 years]

    clinical features and objective findings of the acute phase of the TBE-patients diagnosed with TBE in South-East Norway during 2018-2021

  2. To investigate the impact of TBEV infection on health-related QOL in a one year follow-up study of a Norwegian patient cohort [4 years]

    A prospective multicenter study of health-related QOL one year after hospitalization with TBE in South-East Norway from 2019-2022. The self-reported health-related QOL (assessed by SF-36) of the TBE-patients, will be compared with the SF-36 reference values in the Norwegian population.

  3. To investigate the impact of TBEV infection on long-term cognitive function in a one year follow-up study of a Norwegian patient cohort [5 years]

    A prospective multicenter study of self-reported cognitive function by BRIEF, FSS, HADS and EMQ, one year after hospitalization with TBE in South-East Norway from 2019-2022. The cognitive function, measured by PROMS, will be compared with PROMS from an included reference group from the patient's social environment.

  4. To identify biomarkers in the cerebrospinal fluid (CSF) and blood, which serve as predictors for TBE severity and long-term complaints [5 years]

    FS-36 and BRIEF

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  1. Patient: The patients diagnosed with acute infection with TBEV at admission.

  2. Control: same age (plus/minus 4 years), level of education (plus minus 2 years) and the same gender as patient.

Exclusion Criteria:
  1. Patient: Patients who turn out to have different diagnose than acute infections with TBEV.

  2. Control: Previously infection with tick-borne encephalitis virus.

  3. The patients who were diagnosed with typical symptoms and only TBEV IgM-test must take a blood sample for IgG analyses. If the TBE IgG analysis is negative, the patient will be excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sykehuset Telemark HF Skien Telemark Norway 3710
2 Sykehuset Sørlandet HF Arendal Norway
3 Sykehuset i Vestfold Tønsberg Norway

Sponsors and Collaborators

  • Sykehuset Telemark
  • Sykehuset i Vestfold HF
  • Norwegian Institute of Public Health
  • Sorlandet Hospital HF
  • Oslo University Hospital

Investigators

  • Study Director: Hege Kersten, PhD, Study director

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sykehuset Telemark
ClinicalTrials.gov Identifier:
NCT05138055
Other Study ID Numbers:
  • 96505
First Posted:
Nov 30, 2021
Last Update Posted:
Nov 30, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 30, 2021