ClinicalTrials.Veeva

Menu

Medical In-Patient Rehabilitation in Rheumatoid Arthritis

U

University of Luebeck

Status and phase

Completed
Phase 3

Conditions

Rheumatoid Arthritis

Treatments

Procedure: Counselling and 3-week medical in-patient rehabilitation

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00229541
FKZ 01GL0306

Details and patient eligibility

About

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.

Full description

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:

  1. 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)
  2. screening questionnaire to verify in-/exclusion criteria
  3. selection of eligible insurants (RA-criteria of American College of Rheumatology, clinical expert)
  4. baseline measurement (e.g. SF-36, RAQoL, FFbH-P, SPE)
  5. external stratified block by block randomization: intervention group (3- week medical in-patient rehabilitation) vs. control group (usual care)
  6. follow-up measurement (12 months after baseline)
  7. 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.

Enrollment

129 patients

Sex

All

Ages

20 to 62 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

129 participants in 2 patient groups

IG
Experimental group
Description:
intervention group, receives counselling on medical inpatient rehabilitation by statutory health insurance, is intended to apply for a 3-wek medical inpatient rehabilitation at the co-operating clinic (Bad Bramstedt)
Treatment:
Procedure: Counselling and 3-week medical in-patient rehabilitation
KG
No Intervention group
Description:
control group, receives usual care

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems