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Completed

NCT Number: NCT00229541

Medical In-Patient Rehabilitation in Rheumatoid Arthritis

The randomised controlled trial explores the efficacy of a counselling interview on an multidisciplinary multimodal intervention to ameliorate the somatic, mental and social medical progress of rheumatoid arthritis in gainfully employed insurants of compulsory health insurances and statutory pension insurances . Additionally, the feasibility to recruit a study population via databases of compulsory health insurances is examined.

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Key information

Age range

20 year–62 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Institute for Social Medicine, University of Luebeck

Lübeck, 23538, Germany

About this study

Rheumatoid arthritis is the most prevalent inflammatory rheumatic disease. Limited participation of the individual patient accumulates with large amounts of indirect costs for society: About 40 % of the affected patients have to quit their jobs within the first three to four years after disease onset. Nevertheless, the German health care system still seems to lack an adequate supply, particularly in case of medical rehabilitation in early stages of disease. International clinical trials, reviews amd evidence-based guidelines emphasize the importance of an early multimodal multidisciplinary team care as in Germany provided by specialised clinics through three-week in-patient medical rehabilitation programs. The available study explores the efficacy of a counselling interview on an medical in-patient rehabilitation in a randomised controlled design. Exclusively, gainfully employed insurants of compulsory health insurances and statutory pension insurances are included in the study.

Secondary, to avoid the problem of a selection bias caused by recruitment via clinics or doctors, the RCT tests the possibility to recruit potential participants by data of the co-operating health insurances on RA-specific diagnoses of work incapacity, hospital discharge diagnoses, and medical prescriptions within the past 24 months.

Detailed process:

  • Recruitment of a potential study population via health insurance data (defined search criteria: ICD-10 diagnoses M05/06/13/79 in case of work disability/hospital discharge, RA-specific medical prescriptions within the past 24 months)
  • screening questionnaire to verify in-/exclusion criteria
  • selection of eligible insurants (RA-criteria of American College of Rheumatology, clinical expert)
  • baseline measurement (e.g. SF-36, RAQoL, FFbH-P, SPE)
  • external stratified block by block randomization: intervention group (3- week medical in-patient rehabilitation) vs. control group (usual care)
  • follow-up measurement (12 months after baseline)
  • data transfer of health insurances and pension insurances

Comparison:

Looking at a 12-months follow-up, the intervention group (3-week medical in-patient rehabilitation) is expected to show significant enhancement in somatic, mental and social medical parameters concerning rheumatoid arthritis compared to a control group receiving usual care.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Rheumatoid arthritis / psoriatic arthritis (expert decision, ACR criteria)
  • Insurant of co-operating health insurance and pension insurance
  • Gainfully employed
  • Eligible to receive a medical in-patient rehabilitation

Exclusion criteria

  • Polyarthritis, inflammatory intestinal diseases and diseases of connective tissue
  • Currently work disabled
  • Not able / not willing to co-operate
  • Medical in-patient rehabilitation within past 48 months

Treatment and study plan

Counselling and 3-week medical in-patient rehabilitation

Procedure

Counselling and 3-week medical in-patient rehabilitation in IG

Primary outcomes

  1. work incapacity (incidence, duration)

    Time frame: baseline, 12 months follow-up

Secondary outcomes

  1. general health status (SF-36)

    Time frame: baseline, 12 months follow-up

  2. Functional capacity (FFbH-P)

    Time frame: baseline, 12 months follow-up

  3. Quality of life (RAQoL)

    Time frame: baseline

  4. Subjective prognosis of gainful employment (SPE-scale)

    Time frame: baseline, 12 months follow-up

  5. Somatization (SCL-90-R)

    Time frame: baseline, 12 months follow-up

  6. Depression

    Time frame: baseline, 12 months follow-up

Sponsors and collaborators

Lead sponsor

University of Luebeck

Other

Collaborators

  • AOK Schleswig-Holstein
  • BEK Nord
  • Berufsverband Deutscher Rheumatologen
  • BfA
  • DAK Gesundheit
  • Deutsche Rheumaliga Schleswig-Holstein
  • Draeger and Hanse BKK
  • IKK Schleswig-Holstein
  • LVA Schleswig-Holstein
  • TK Schleswig-Holstein

Registry information

Official study title

Medical In-Patient Rehabilitation in Rheumatoid Arthritis: Acceptance and Outcomes in Insurants of Compulsory Health Insurances and Statutory Pension Insurances (VERA)

Important dates

Study start
2003
Study completion
2006
First posted
Sep 29, 2005
Registry last updated
Oct 29, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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