The efficacy and predicting variables of a multidisciplinary disability resolution (MDR) program for CFS patients recieving long term disability benefits from income protection insurers.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON21294

Enrollment

130

Registered

2006-03-07

Start date

2006-04-01

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

MDR

Interventions

Patients in the intervention group will recieve a highly individualised treatment by experts on different fields of expertise (i.e. medical, psychological, physical, legal). A major part of this treat

Eligibility

Inclusion criteria

Inclusion criteria: Patients are included with: 1. Extreme fatigue; 2. With considerable impairment in daily functioning; 3. Disease (objective finding) - illness (subjective complaints) discrepancy present; 4. Not older than 45 years; 5. Recieving disability benefits for a period longer than 3 years.

Exclusion criteria

Exclusion criteria: Patients with: 1. A disease present that can explain the fatigue; 2. A history of psychosis or schizophrenia; 3. Primary drugs or alcohol abuse.

Design outcomes

Primary

Measure	Time frame
Off-claim and number of hours in a paid job.	—

Secondary

Measure	Time frame
1. Fatigue severity; 2. Functional impairment; 3. Physical limitations; 4. Psychological well-being; 5. Pain.	—

Contacts

Public ContactH. Vissers

University Medical Center St. Radboud, Expert Center Chronic Fatigue, 4628, P.O. Box 9101

H.Vissers@nkcv.umcn.nl+31 (0)24 3610046

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)