Nursing Consultation in Out-patient Clinics for Patients With Inflammatory Rheumatic Disease
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Purpose
Evaluate the effectiveness and acceptability of care given by nurse specialists in out patient clinics, through a randomized controlled study.
| Condition | Intervention |
|---|---|
|
Arthritis |
Other: Follow up bu a nurse Other: Follow up by a medical doctor |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Nursing Consultation in Out-patient Clinics for Patients With Inflammatory Rheumatic Disease |
- patient satisfaction [ Time Frame: 12 mnths and 24 mnths ] [ Designated as safety issue: No ]
- Health related quality of life [ Time Frame: 12 mnths and 24 mnths ] [ Designated as safety issue: No ]
- Disease activity [ Time Frame: 12 mnths and 24 mnths ] [ Designated as safety issue: No ]
- coping [ Time Frame: 12 mnths and 24 mnths ] [ Designated as safety issue: No ]
| Enrollment: | 68 |
| Study Start Date: | September 2005 |
| Study Completion Date: | August 2008 |
| Primary Completion Date: | August 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Follow up by nurse
Patient randomized for follow-up by a nurse
|
Other: Follow up bu a nurse
Follow up bu a nurse
|
|
Experimental: follow up by medical doctor
Patients randomized for follow up by a medical doctor
|
Other: Follow up by a medical doctor
Follow up by a medical doctor
|
Detailed Description:
This study is part of a national multicenter study (NOR-DMARD) that aims to measure the longterm safety and effectiveness of disease modifying therapies in inflammatory arthropathies. The Nor-Dmard study is a comparative, phase IV, longitudinal, observational study. All patients starting a DMARD regime are enrolled. Patients from two clinics (different parts of Norway) will be randomised to receive follow-up care from either a clinical nurse or a rheumatologist.
The primary outcome measure is patient satisfaction measured by Leeds Satisfaction Questionnaire.
The secondary outcome is effectiveness measured by Coping (CORS),Health related quality of life (SF-36) and Disease activity (MHAQ, DAS-28).
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients with inflammatory arthropathies monitored after starting disease modifying antirheumatic drugs.
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Hege Svean Koksvik, Research Nurse, Diakonhjemmet Hospital |
| ClinicalTrials.gov Identifier: | NCT00403676 History of Changes |
| Other Study ID Numbers: | DiakonhjemmetS |
| Study First Received: | November 24, 2006 |
| Last Updated: | June 27, 2012 |
| Health Authority: | Norway:National Committee for Medical and Health Research Ethics |
Keywords provided by Diakonhjemmet Hospital:
|
nurse practitioner rheumatology care outpatient clinic patient satisfaction |
Additional relevant MeSH terms:
|
Arthritis Rheumatic Diseases Joint Diseases Musculoskeletal Diseases Connective Tissue Diseases |
ClinicalTrials.gov processed this record on May 19, 2013