Evaluating the Effectiveness of a Chronic Disease Management Program for Gout
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Purpose
The aim of this study is to test the effectiveness of a pharmacist-staffed, protocol-based chronic disease management program compared to patients receiving usual care in achieving a target serum uric acid level in patients with recurrent gout.
| Condition | Intervention |
|---|---|
|
Recurrent or Tophacous Gout |
Other: Control Other: Gout Disease Management Program |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Evaluating the Effectiveness of a Chronic Disease Management Program for Gout |
- Serum Uric Acid Level [ Time Frame: change from baseline at 6 months follow up ] [ Designated as safety issue: No ]attainment and maintenance of a serum uric acid level of 6.0 mg/dl or less. The outcome will be considered positive if that level is attained and the 6 month follow up value remains at the target level.
- Serum Creatinine [ Time Frame: 0, 12, and 26 weeks ] [ Designated as safety issue: No ]Change in Serum Creatinine
- Serum Alanine Aminotransferase (ALT) [ Time Frame: 0, 12, and 26 weeks ] [ Designated as safety issue: No ]Change in serum ALT (a measure of potential toxicity)
- Gout flares [ Time Frame: 0, 12, and 26 weeks ] [ Designated as safety issue: No ]Number of gout flares
| Estimated Enrollment: | 98 |
| Study Start Date: | January 2012 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Gout Chronic Disease Management Program |
Other: Gout Disease Management Program
The experimental group will utilize standard guidelines for the initiation of uric acid lowering treatments, and approved medications. The study protocol treatments include medication management, dietary guidelines, and basic educational materials on gout and its management. No non-formulary medications or devices will be used. The experimental procedure to be tested is the use of a structured protocol to manage and monitor standard treatments.
|
| Active Comparator: Usual Care |
Other: Control
The control group will receive care from their primary care physician that refelects the actual current care received by KPNC patients, but will not receive any treatment recommendations from the study protocol. The control subject will have regular monitoring of serum uric acid levels and will be provided with educational material and dietary counseling.
|
Detailed Description:
Gout is a chronic condition with intermittent symptoms and should be managed through an outcome-based disease management approach. Unlike other common chronic conditions, strategies for population management in gout patients have not been tested. The study will identify adult members of Kaiser Permanente (KP) Northern California with a diagnosis of gout and 3 or more outpatient or Emergency Department visits for gout over a 1-year period preceding study enrollment. These patients will be randomized to either an active management group, or to usual care. The participants will be enrolled and followed over a period of 26 weeks. The primary outcome to be measured will be the attainment and maintenance of a uric acid lowering regimen targeted to achieve serum uric acid level of 6.0 mg/dl or less. The treatment protocol will use standard treatment guidelines to lower and maintain uric acid levels to less than or equal to 6.0 mg/dl (or maximum doses of uric acid lowering medications) and provide patient education and dietary counseling. Monitoring and medication management will be carried out by a licensed clinical pharmacist under the supervision of an experienced rheumatologist. Control subjects will have regular monitoring of serum uric acid levels and will be provided with educational material and dietary counseling, but otherwise receive usual care. The demonstration that a chronic disease management approach to gout care can improve the health and reduce morbidity in patients with gout may illuminate a simple path towards improved quality of life and reduced morbidity in this growing population of patients.
Eligibility| Ages Eligible for Study: | 21 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Three or more outpatient/ED visits in a 24-month period prior to selection for study with one of these primary visit diagnoses:
- Gouty arthropathy
- Gout, unspecified
- Gout with other specified manifestations
- Tophaceous gout of ear (274.81) or other sites
- Gouty nephropathy
At least 2 years of continuous Kaiser Foundation Hospital Plan membership
Baseline uric acid level above 7.0mg/dl
Exclusion Criteria:
- Current cancer diagnosis with active treatment
- End stage renal disease
- Pregnant or lactating
- Patients with a diagnosis of dementia
- Terminally ill patients
Contacts and Locations| Contact: Robert Goldfien, MD | 510-307-2658 | robert.goldfien@kp.org |
| Contact: Andy Avins, MD | 510-891-3557 | andy.l.avins@kp.org |
| United States, California | |
| Kaiser Permanente Northern California Medical Facilities | Recruiting |
| All KPNC Facilities, California, United States | |
| Principal Investigator: | Robert Goldfien, MD | Kaiser Permanente Northern California |
More Information
No publications provided
| Responsible Party: | Kaiser Permanente |
| ClinicalTrials.gov Identifier: | NCT01568879 History of Changes |
| Other Study ID Numbers: | CN-11RGold-02-H |
| Study First Received: | March 28, 2012 |
| Last Updated: | October 30, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Kaiser Permanente:
|
Recurrent gout Tophacous gout Gout flares |
Arthritis Joint Diseases Rheumatic Diseases |
Additional relevant MeSH terms:
|
Chronic Disease Gout Disease Attributes Pathologic Processes Arthritis Joint Diseases |
Musculoskeletal Diseases Rheumatic Diseases Purine-Pyrimidine Metabolism, Inborn Errors Metabolism, Inborn Errors Genetic Diseases, Inborn Metabolic Diseases |
ClinicalTrials.gov processed this record on May 21, 2013