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Mental Training for CFS Following EBV Infection in Adolescents

Primary Purpose

Fatigue Syndrome, Chronic, Epstein-Barr Virus Infection

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Mental training
Sponsored by
University Hospital, Akershus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fatigue Syndrome, Chronic

Eligibility Criteria

12 Years - 20 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participant in the research project CEBA (Chronic fatigue following acute Epstein-Barr virus infection in adolescents, NCT02335437)
  • Chronic fatigue at 6 months (a sum score of dichotomized responses ≥ 4 on the Chalder Fatigue questionnaire)

Exclusion Criteria:

  • Other illnesses that might explain the fatigue
  • Bedridden

Sites / Locations

  • Dept. of Pediatrics, Akershus University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Mental training

Routine follow-up

Arm Description

The intervention consists of one introductory session (patients and their parents/next-of-kin), followed by 9 individual therapy sessions (one each week) of 1.5 hours duration and related home-work, combining elements from cognitive behavioural therapy and music therapy: Important elements of the mental training program are: Psychoeducation: Theories of CFS/ME pathophysiology and treatment rationale Relaxation: Bodily stress reduction, mindfulness Visualization: Contact with positive emotions, techniques of worrying reduction Experiences: Behavioral 'experiments' (individually adjusted), 'trick into action' Cognitive challenges: Challenging thoughts about disease process, stimulus and outcome expectancies, prognosis

Routine follow-up by the general practitioner, which is normal approach to chronic fatigue following acute EBV infection.

Outcomes

Primary Outcome Measures

Physical activity
Mean steps/day during 7 consecutive days measured by accelerometer

Secondary Outcome Measures

Plasma catecholamines
Plasma catecholamines
Urine cortisol:creatinin ratio
Urine cortisol:creatinin ratio
Degree centrality index of cytokine network
An index of node centrality, based upon network analyses
Degree centrality index of cytokine network
An index of node centrality, based upon network analyses
Number of NK-cells
Number of NK-cells
Supine heart rate
Supine heart rate
Heart rate variability indices
Heart rate variability indices
Heart rate, blood pressure and total peripheral resistence responses to upright posture
Heart rate, blood pressure and total peripheral resistence responses to upright posture
Working memory
Digit span forward and backward test
Working memory
Digit span forward and backward test
Cognitive inhibition
Color-word interference test from the D-KEFS instrument
Cognitive inhibition
Color-word interference test from the D-KEFS instrument
Correlation matrix indices of regions of interests (ROIs) in the brain salience network
Functional connectivity analyses from resting state brain fMRI
Correlation matrix indices of regions of interests (ROIs) in the brain salience network
Functional connectivity analyses from resting state brain fMRI
Fatigue score (Chalder fatigue questionnaire)
Fatigue score (Chalder fatigue questionnaire)
Pain scores (Brief pain Inventory)
Pain scores (Brief pain Inventory)
Quality of Life score (PedsQL)
Quality of Life score (PedsQL)
Anxiety and depression score (HADS)
Anxiety and depression score (HADS)
Alexithymia score (TAS-20)
Alexithymia score (TAS-20)
Insomnia score (KSQ)
Insomnia score (KSQ)
Pain threshold (algometry)
Pain threshold (algometry)
Disability score (FDI)
Disability score (FDI)
Side effect and unexpected events questionnaire
Side effect and unexpected events questionnaire
Side effect and unexpected events questionnaire
Side effect and unexpected events questionnaire
Physical activity
Mean steps/day during 7 consecutive days measured by accelerometer

Full Information

First Posted
July 9, 2015
Last Updated
February 14, 2022
Sponsor
University Hospital, Akershus
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1. Study Identification

Unique Protocol Identification Number
NCT02499302
Brief Title
Mental Training for CFS Following EBV Infection in Adolescents
Official Title
Mental Training for Chronic Fatigue Syndrome (CFS/ME) Following EBV Infection in Adolescents: A Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
October 2015 (Actual)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
October 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Akershus

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The general aim of this study is to investigate the effect of an individually tailored mental training program in adolescents developing chronic fatigue syndrome (CFS) after an acute Epstein Barr-virus (EBV) infection. Endpoints include physical activity (primary endpoint), symptoms (fatigue, pain, insomnia), cognitive function (executive functions) and markers of disease mechanisms (autonomic, endocrine, and immune responses).
Detailed Description
EBV-infection is a well-known trigger of CFS. A closely related research project (Chronic fatigue following acute Epstein-Barr virus infection in Adolescents; ClinicalTrials ID:NCT02335437) is a combined prospective and cross-sectional study of 200 adolescents suffering from acute EBV infection. The primary aim of that study is to identify factors that predispose to CFS 6 months after the acute infection. Thus, that project will provide a sample of thoroughly characterized CFS patients, all having the same precipitation factor (EBV-infection). The present project is an intervention trial in the subgroup of patients that actually did develop CFS 6 months after the acute EBV infection. Patients will be randomised 1:1 to either a mental training program (10 sessions) combining elements from cognitive behavioral therapy and music therapy, or routine follow-up from the general practitioner. By its nature, treatment group allocation cannot be blinded; however, both patients and therapists will be blinded for end-point evaluation. An extensive investigational program will be carried out at three time points: Prior to the intervention, immediately after the intervention, and 1 year after the intervention. The program includes: Clinical examination; Pain threshold assessment; Cardiovascular assessment; Cognitive assessment; Sampling of biological material (blood and urine); Questionnaire; Brain fMRI; Qualitative interview; Monitoring of physical activity (accelerometer)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatigue Syndrome, Chronic, Epstein-Barr Virus Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mental training
Arm Type
Experimental
Arm Description
The intervention consists of one introductory session (patients and their parents/next-of-kin), followed by 9 individual therapy sessions (one each week) of 1.5 hours duration and related home-work, combining elements from cognitive behavioural therapy and music therapy: Important elements of the mental training program are: Psychoeducation: Theories of CFS/ME pathophysiology and treatment rationale Relaxation: Bodily stress reduction, mindfulness Visualization: Contact with positive emotions, techniques of worrying reduction Experiences: Behavioral 'experiments' (individually adjusted), 'trick into action' Cognitive challenges: Challenging thoughts about disease process, stimulus and outcome expectancies, prognosis
Arm Title
Routine follow-up
Arm Type
No Intervention
Arm Description
Routine follow-up by the general practitioner, which is normal approach to chronic fatigue following acute EBV infection.
Intervention Type
Behavioral
Intervention Name(s)
Mental training
Primary Outcome Measure Information:
Title
Physical activity
Description
Mean steps/day during 7 consecutive days measured by accelerometer
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Plasma catecholamines
Time Frame
12 weeks
Title
Plasma catecholamines
Time Frame
64 weeks
Title
Urine cortisol:creatinin ratio
Time Frame
12 weeks
Title
Urine cortisol:creatinin ratio
Time Frame
64 weeks
Title
Degree centrality index of cytokine network
Description
An index of node centrality, based upon network analyses
Time Frame
12 weeks
Title
Degree centrality index of cytokine network
Description
An index of node centrality, based upon network analyses
Time Frame
64 weeks
Title
Number of NK-cells
Time Frame
12 weeks
Title
Number of NK-cells
Time Frame
64 weeks
Title
Supine heart rate
Time Frame
12 weeks
Title
Supine heart rate
Time Frame
64 weeks
Title
Heart rate variability indices
Time Frame
12 weeks
Title
Heart rate variability indices
Time Frame
64 weeks
Title
Heart rate, blood pressure and total peripheral resistence responses to upright posture
Time Frame
12 weeks
Title
Heart rate, blood pressure and total peripheral resistence responses to upright posture
Time Frame
64 weeks
Title
Working memory
Description
Digit span forward and backward test
Time Frame
12 weeks
Title
Working memory
Description
Digit span forward and backward test
Time Frame
64 weeks
Title
Cognitive inhibition
Description
Color-word interference test from the D-KEFS instrument
Time Frame
12 weeks
Title
Cognitive inhibition
Description
Color-word interference test from the D-KEFS instrument
Time Frame
64 weeks
Title
Correlation matrix indices of regions of interests (ROIs) in the brain salience network
Description
Functional connectivity analyses from resting state brain fMRI
Time Frame
12 weeks
Title
Correlation matrix indices of regions of interests (ROIs) in the brain salience network
Description
Functional connectivity analyses from resting state brain fMRI
Time Frame
64 weeks
Title
Fatigue score (Chalder fatigue questionnaire)
Time Frame
12 weeks
Title
Fatigue score (Chalder fatigue questionnaire)
Time Frame
64 weeks
Title
Pain scores (Brief pain Inventory)
Time Frame
12 weeks
Title
Pain scores (Brief pain Inventory)
Time Frame
64 weeks
Title
Quality of Life score (PedsQL)
Time Frame
12 weeks
Title
Quality of Life score (PedsQL)
Time Frame
64 weeks
Title
Anxiety and depression score (HADS)
Time Frame
12 weeks
Title
Anxiety and depression score (HADS)
Time Frame
64 weeks
Title
Alexithymia score (TAS-20)
Time Frame
12 weeks
Title
Alexithymia score (TAS-20)
Time Frame
64 weeks
Title
Insomnia score (KSQ)
Time Frame
12 weeks
Title
Insomnia score (KSQ)
Time Frame
64 weeks
Title
Pain threshold (algometry)
Time Frame
12 weeks
Title
Pain threshold (algometry)
Time Frame
64 weeks
Title
Disability score (FDI)
Time Frame
12 weeks
Title
Disability score (FDI)
Time Frame
64 weeks
Title
Side effect and unexpected events questionnaire
Time Frame
3 weeks
Title
Side effect and unexpected events questionnaire
Time Frame
6 weeks
Title
Side effect and unexpected events questionnaire
Time Frame
9 weeks
Title
Side effect and unexpected events questionnaire
Time Frame
12 weeks
Title
Physical activity
Description
Mean steps/day during 7 consecutive days measured by accelerometer
Time Frame
64 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participant in the research project CEBA (Chronic fatigue following acute Epstein-Barr virus infection in adolescents, NCT02335437) Chronic fatigue at 6 months (a sum score of dichotomized responses ≥ 4 on the Chalder Fatigue questionnaire) Exclusion Criteria: Other illnesses that might explain the fatigue Bedridden
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vegard Bruun Wyller, PhD
Organizational Affiliation
University Hospital, Akershus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept. of Pediatrics, Akershus University Hospital
City
Lørenskog
State/Province
Akershus
ZIP/Postal Code
N-1478
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
33117895
Citation
Malik S, Asprusten TT, Pedersen M, Mangersnes J, Trondalen G, van Roy B, Skovlund E, Wyller VB. Cognitive-behavioural therapy combined with music therapy for chronic fatigue following Epstein-Barr virus infection in adolescents: a randomised controlled trial. BMJ Paediatr Open. 2020 Oct 21;4(1):e000797. doi: 10.1136/bmjpo-2020-000797. eCollection 2020.
Results Reference
derived
PubMed Identifier
32342016
Citation
Malik S, Asprusten TT, Pedersen M, Mangersnes J, Trondalen G, van Roy B, Skovlund E, Wyller VB. Cognitive-behavioural therapy combined with music therapy for chronic fatigue following Epstein-Barr virus infection in adolescents: a feasibility study. BMJ Paediatr Open. 2020 Apr 9;4(1):e000620. doi: 10.1136/bmjpo-2019-000620. eCollection 2020.
Results Reference
derived

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Mental Training for CFS Following EBV Infection in Adolescents

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