Skip to content

Chronic Fatigue Following Acute Epstein-Barr Virus Infection in Adolescents

Chronic Fatigue Following Acute Epstein-Barr Virus Infection in Adolescents

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02335437
Acronym
CEBA
Enrollment
270
Registered
2015-01-09
Start date
2015-03-31
Completion date
2017-06-30
Last updated
2017-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epstein-Barr Virus Infections, Fatigue Syndrome, Chronic

Brief summary

Chronic fatigue syndrome (CFS) is characterized by unexplained, disabling and long lasting fatigue, as well as pain, impaired memory, sleep difficulties and other symptoms. Epstein-Barr virus (EBV) infection might precipitate CFS. In this study, 200 adolescents undergoing acute EBV infection will be followed prospectively, and also compared with a group of healthy controls. The aim is twofold: * To identify factors that predispose to chronic fatigue among adolescents with acute EBV infection * To compare pathophysiological features of patients with acute EBV infection with a group of healthy controls. Possible risk factors for chronic fatigue 6 months after EBV-infection includes: * Severity of the initial infection * Immune responses characteristics * Characteristics of the neuroendocrine stress response * Cognitive functioning * Emotional disturbances * Genetics/ epigenetics of candidate genes * Certain personality traits * Critical life events

Interventions

None listed

Sponsors

University Hospital, Akershus
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to 20 Years
Healthy volunteers
Yes

Inclusion criteria

* Age ≥ 12 years and \< 20 years * Serological confirmation of acute EBV infection * Lives in one of the following Norwegian counties: Oslo, Akershus, Buskerud, Østfold, Vestfold

Exclusion criteria

* Medical treatment for another disease (hormonal conterception and antibiotics against tonsillitis/pharyngitis are accepted) * Pregnancy * Debut of illness \> 6 weeks ago

Design outcomes

Primary

MeasureTime frameDescription
Fatigue6 monhtsChalder fatigue questionnaire, total score
Steps per day6 monhtsMean number of steps/day across 7 consecutive days, measured by accelerometer (ActivePal)

Secondary

MeasureTime frameDescription
Cognitive function6 monhtsAssessed by the instruments WISC-IV, D-KEFS, HVLT-R and WASI.
Neuroendocrine markers6 monhtsIn particular blood and urine measurements of catecholamines and the HPA axis
Immune markers6 monhtsIn particular blood measurements of cytokines
Pain threshold6 monhtsAssessed by pressure algometry
Quality of life6 monhtsAssessed by the PedsQL inventory
Functional disability6 monhtsAssessed by the FDI inventory
Bodily symptoms6 monhtsAssessed by different questionnaires
Autonomic cardiovascular control6 monhtsAssessed by noninvasive, continuous recordings of heart rate, blood pressures and stroke volume during supine rest.

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026