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Clinical Trials/NL-OMON39182
NL-OMON39182
Completed
N/A

*Is a multidisciplinary rehabilitation treatment more effective than monodisciplinary cognitive behavioural therapy for patients with chronic fatigue syndrome? A multicentre randomised controlled trial* - FatiGo (Fatigue-Go-trial)

Revant, Revalidatiecentrum Breda0 sites122 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Revant, Revalidatiecentrum Breda
Enrollment
122
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Revant, Revalidatiecentrum Breda

Eligibility Criteria

Inclusion Criteria

  • Patients are included if they fulfil the CDC\-94 criteria for CFS and score more or equal to 40 on the Checklist Individual Strength (CIS)\-fatigue questionnaire (Prins et al. 2001\).
  • CDC\-94 criteria for CFS are as follows:
  • At least 6 months of persistent or recurring fatigue for which no physical explanation has been found and which:
  • \- is of new onset, that is to say it has not been lifelong
  • \- is not the result of ongoing exertion
  • \- is not substantially alleviated by rest
  • \- severely limits functioning
  • In combination with four or more of the following symptoms, persistent or regularly recurring over a period of 6 months and which must not have predated the fatigue:
  • \- self\-reported impairment in memory or concentration
  • \- sore throat

Exclusion Criteria

  • Exclusion criteria
  • \- any medical condition that may explain the presence of chronic fatigue
  • \- a psychotic, major or bipolar depressive disorder (but not an uncomplicated depression)
  • \- dementia
  • \- anorexia or bulimia nervosa
  • \- alcohol abuse or the use of drugs
  • \- severe obesity
  • \- pregnancy
  • \- not able to speak, understand or read the Dutch language
  • \- patients who had CGT or rehabilitation therapy in the past involving CFS.

Outcomes

Primary Outcomes

Not specified

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