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Effects of a minimal cognitive behaviour therapy (CBT) intervention for patients with chronic fatigue syndrome (CFS) in primary care: a randomised controlled trial - a first step towards stepped care-

Effects of a minimal cognitive behaviour therapy (CBT) intervention for patients with chronic fatigue syndrome (CFS) in primary care: a randomised controlled trial - a first step towards stepped care-

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28082
Enrollment
120
Registered
2008-02-29
Start date
2008-03-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Chronic Fatigue Syndrome (CFS) Chronische Vermoeidheid Syndroom

Interventions

After a baseline assessment (T1) patients are randomly assigned to the intervention- or waiting list condition. The patients in the intervention condition start immediately with minimal intervention.

Sponsors

Radboud University Nijmegen Medical Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. CDC criteria for CFS 2. Age between 18-65 years 3. Able to speak, read and write Dutch language 4. CIS fatigue score of 35 or higher, indicating severe fatigue 5. SF 36 physical and/or social functioning score of 70 or below.

Exclusion criteria

Exclusion criteria: 1. Patient does not meet the therefore mentioned inclusion criteria 2. Patient is currently engaged in a legal procedure concerning disability-related financial benefits.

Design outcomes

Primary

MeasureTime frame
The primary outcome variables are fatigue severity and functional disability. The Checklist Individual Strength (CIS) subscale for fatigue indicates the level of experienced fatigue over the past 2-week period. To measure the level of disability the Medical Outcomes Survey Short From (SF-36) is used. Physical and social disabilities are measured with the 'physical functioning' and 'social functioning' subscale fo the SF-36.

Secondary

MeasureTime frame
The secondary outcome measure is the level of psychological distress measured with the Symptom Checklist 90 (SCL-90).

Contacts

Public ContactM. Tummers

Radboud University Nijmegen Medical Centre 4628 Expert Centre Chronic Fatigue P.O. box 9101

M.Tummers@nkcv.umcn.nl+31 (0) 243610048

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)