Patient and Provider Interventions for Managing Osteoarthritis in Primary Care
Primary Purpose
Osteoarthritis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Osteoarthritis Intervention
Sponsored by
About this trial
This is an interventional health services research trial for Osteoarthritis focused on measuring Osteoarthritis, Exercise, Diet, Coping Skills, Education, Medical
Eligibility Criteria
Inclusion Criteria:
- radiographic evidence of hip OA and / or radiographic of or meets clinical criteria for knee OA
- current joint symptoms
- BMI >=25
- physically inactive
Exclusion Criteria:
- Diagnosis of rheumatoid arthritis, fibromyalgia, or other systemic rheumatic disease
- Hospitalized for a stroke, myocardial infarction or coronary artery revascularization in the past 3 months
- Active diagnosis of psychosis or serious personality disorder
- On waiting list for / planning arthroplasty
- Severely impaired hearing or speech (patients must be able to respond to phone calls)
- Unable to speak English
- No access to a telephone
- Participating in another OA intervention or other lifestyle change study
- Dementia or other memory loss condition
- Current, uncontrolled substance abuse disorder
- Motor neuron diseases, Parkinson's Disease, multiple sclerosis
- Quadriplegic or paraplegic
- Serious / terminal illness as indicated by referral to hospice or palliative care
- Other self-reported health problem that would prohibit participation in the study
- Nursing home resident
- Other health conditions or personal issues judged by a study team member or primary care physician to make the patient inappropriate for the study
- Female participants: pregnant or planning to become pregnant
- Metastatic Cancer
- History of gout in knee or hip
- Total joint replacement (knee or hip) surgery, other knee or hip surgery, meniscus tear (verified by MRI), or ACL tear in the past 6 months
- Have not seen their VA-assigned primary health care provider for more than a year
Sites / Locations
- Durham VA Medical Center, Durham, NC
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Arm 1
Arm 2
Arm Description
usual care
Osteoarthritis Intervention - Primary care providers receive patient-specific osteoarthritis information and treatment recommendations approximately one week prior to the patient's first post-enrollment routine appointment with PCP; patients receive a 12-month intervention consisting of monthly phone calls focusing on exercise, weight management, and cognitive behavioral pain management.
Outcomes
Primary Outcome Measures
Western Ontario and McMasters Universities Osteoarthritis Index (WOMAC)
Self-report measure of lower extremity pain (5 items), stiffness (2 items), and function (17 items) in the past two weeks. All items are rated on a 5-point Likert scale ranging from "none" (0) to "severe / extreme" (4), for a total of range of 0-96. Higher scores indicate worse symptoms and poorer function. The Mixed Models Analysis described below utilizes a common baseline mean rather than means for the individual arms. This common baseline mean is presented here, and the raw baseline measures per group are presented in the baseline information section.
Secondary Outcome Measures
Short Physical Performance Test Protocol
This is a series of 5 tests covering the domains of balance (3 tests), gait speed (8 foot walk) and time to rise from a chair and return to the seated position five times. The total score ranges from 0 (worst performance) to 12 (best performance).
The Mixed Models Analysis described below utilizes a common baseline mean rather than means for the individual arms. This common baseline mean is presented here, and the raw baseline measures per group are presented in the baseline information section.
PHQ-8
This is an 8-item self-report scale, all items are rated on a score of 0-3, for a total range of 0-24. Higher scores indicate more depressive symptoms. The Mixed Models Analysis described below utilizes a common baseline mean rather than means for the individual arms. This common baseline mean is presented here, and the raw baseline measures per group are presented in the baseline information section.
Full Information
NCT ID
NCT01130740
First Posted
May 24, 2010
Last Updated
April 6, 2015
Sponsor
US Department of Veterans Affairs
1. Study Identification
Unique Protocol Identification Number
NCT01130740
Brief Title
Patient and Provider Interventions for Managing Osteoarthritis in Primary Care
Official Title
Patient and Provider Interventions for Managing Osteoarthritis in Primary Care
Study Type
Interventional
2. Study Status
Record Verification Date
September 2014
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
January 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Osteoarthritis (OA) is one of the most common chronic conditions and a leading cause of disability among veterans. Many veterans with OA have significant pain and functional limitations, even though they receive some medical care for their OA. Efforts are needed to help veterans to improve OA-related outcomes. This study will examine a comprehensive approach to helping veterans manage their OA-related symptoms, in the context of a VA clinical setting. The study examines an intervention aimed at helping veterans with behaviors that are known to improve OA-related pain and function (such as exercise, weight management, and coping with pain), as well as helping providers to implement evidence-based recommendations for clinical care. The intervention is relatively low cost and easy to disseminate, with the patient component being telephone based. Therefore, if effective, this intervention could be implemented widely across the VA healthcare system.
Detailed Description
Evidence-based guidelines emphasize that adequate management of osteoarthritis (OA) requires a combination of both medical and behavioral modalities. However, many of the recommended guidelines are not regularly incorporated into clinical practice, and the recommended behavioral strategies (e.g. exercise and weight management) are not practiced by most patients. The objective of this study is examine the effectiveness of a combined intervention for patients (involving exercise, weight management, and cognitive behavioral pain management) and providers (involving provision of patient-specific recommendations for care, based on evidence-based guidelines) for improving OA-related outcomes in a real-world VA clinical setting. To our knowledge this is will be the first study to intervene at a both the patient and provider levels for managing OA.
This will be a randomized controlled trial of n=300 patients with symptomatic knee or hip OA, with equal assignment to 2 study arms: 1) Patient and Provider Intervention for OA and 2.) Usual Care Control. We will randomize 30 primary care providers at the Durham VAMC and affiliated community based outpatient clinics to either intervention or control groups. We will then enroll 10 patients from each provider (5 White, 5 Non-White). The patient component of the intervention will be a twelve-month program that includes the following elements: written educational materials (focused on exercise, weight management, and cognitive behavioral pain management), an exercise video tailored for patients with lower extremity OA, and telephone calls by a counselor to support behavior change. The provider component of the intervention will involve giving information on patients' OA symptoms and treatment, as well as patient-specific evidence-based recommendations for care. Providers will have access to this information, as well as facilitated referrals for patient-specific treatment recommendations (e.g. physical therapy, orthopedics), at the point of clinical care, via electronic medical records. The primary time point for outcome assessment will be at 12-months. We will also assess a limited set of outcomes via telephone at 6-months. The primary outcome will be the Western Ontario and McMasters Universities Osteoarthritis Index (WOMAC). Secondary outcomes will include objective physical function (Short Physical Performance Test) and depressive symptoms (PHQ-8). The main study analyses will compare outcomes between the intervention and control groups. We will also assess the cost-effectiveness of the intervention.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis
Keywords
Osteoarthritis, Exercise, Diet, Coping Skills, Education, Medical
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
300 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm 1
Arm Type
No Intervention
Arm Description
usual care
Arm Title
Arm 2
Arm Type
Experimental
Arm Description
Osteoarthritis Intervention - Primary care providers receive patient-specific osteoarthritis information and treatment recommendations approximately one week prior to the patient's first post-enrollment routine appointment with PCP; patients receive a 12-month intervention consisting of monthly phone calls focusing on exercise, weight management, and cognitive behavioral pain management.
Intervention Type
Behavioral
Intervention Name(s)
Osteoarthritis Intervention
Intervention Description
Primary care providers receive patient-specific osteoarthritis information and treatment recommendations two times (0 and 6 months); patients receive a 12-month intervention consisting of monthly phone calls focusing on exercise, weight management, and cognitive behavioral pain management.
Primary Outcome Measure Information:
Title
Western Ontario and McMasters Universities Osteoarthritis Index (WOMAC)
Description
Self-report measure of lower extremity pain (5 items), stiffness (2 items), and function (17 items) in the past two weeks. All items are rated on a 5-point Likert scale ranging from "none" (0) to "severe / extreme" (4), for a total of range of 0-96. Higher scores indicate worse symptoms and poorer function. The Mixed Models Analysis described below utilizes a common baseline mean rather than means for the individual arms. This common baseline mean is presented here, and the raw baseline measures per group are presented in the baseline information section.
Time Frame
12-months
Secondary Outcome Measure Information:
Title
Short Physical Performance Test Protocol
Description
This is a series of 5 tests covering the domains of balance (3 tests), gait speed (8 foot walk) and time to rise from a chair and return to the seated position five times. The total score ranges from 0 (worst performance) to 12 (best performance).
The Mixed Models Analysis described below utilizes a common baseline mean rather than means for the individual arms. This common baseline mean is presented here, and the raw baseline measures per group are presented in the baseline information section.
Time Frame
12-months
Title
PHQ-8
Description
This is an 8-item self-report scale, all items are rated on a score of 0-3, for a total range of 0-24. Higher scores indicate more depressive symptoms. The Mixed Models Analysis described below utilizes a common baseline mean rather than means for the individual arms. This common baseline mean is presented here, and the raw baseline measures per group are presented in the baseline information section.
Time Frame
12-months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
radiographic evidence of hip OA and / or radiographic of or meets clinical criteria for knee OA
current joint symptoms
BMI >=25
physically inactive
Exclusion Criteria:
Diagnosis of rheumatoid arthritis, fibromyalgia, or other systemic rheumatic disease
Hospitalized for a stroke, myocardial infarction or coronary artery revascularization in the past 3 months
Active diagnosis of psychosis or serious personality disorder
On waiting list for / planning arthroplasty
Severely impaired hearing or speech (patients must be able to respond to phone calls)
Unable to speak English
No access to a telephone
Participating in another OA intervention or other lifestyle change study
Dementia or other memory loss condition
Current, uncontrolled substance abuse disorder
Motor neuron diseases, Parkinson's Disease, multiple sclerosis
Quadriplegic or paraplegic
Serious / terminal illness as indicated by referral to hospice or palliative care
Other self-reported health problem that would prohibit participation in the study
Nursing home resident
Other health conditions or personal issues judged by a study team member or primary care physician to make the patient inappropriate for the study
Female participants: pregnant or planning to become pregnant
Metastatic Cancer
History of gout in knee or hip
Total joint replacement (knee or hip) surgery, other knee or hip surgery, meniscus tear (verified by MRI), or ACL tear in the past 6 months
Have not seen their VA-assigned primary health care provider for more than a year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kelli Dominick Allen, PhD
Organizational Affiliation
Durham VA Medical Center, Durham, NC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Durham VA Medical Center, Durham, NC
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
22530979
Citation
Allen KD, Bosworth HB, Brock DS, Chapman JG, Chatterjee R, Coffman CJ, Datta SK, Dolor RJ, Jeffreys AS, Juntilla KA, Kruszewski J, Marbrey LE, McDuffie J, Oddone EZ, Sperber N, Sochacki MP, Stanwyck C, Strauss JL, Yancy WS Jr. Patient and provider interventions for managing osteoarthritis in primary care: protocols for two randomized controlled trials. BMC Musculoskelet Disord. 2012 Apr 24;13:60. doi: 10.1186/1471-2474-13-60.
Results Reference
result
PubMed Identifier
23416927
Citation
Sperber N, Hall KS, Allen K, DeVellis BM, Lewis M, Callahan LF. The role of symptoms and self-efficacy in predicting physical activity change among older adults with arthritis. J Phys Act Health. 2014 Mar;11(3):528-35. doi: 10.1123/jpah.2012-0030. Epub 2013 Feb 8.
Results Reference
result
PubMed Identifier
29523117
Citation
Taylor SS, Hughes JM, Coffman CJ, Jeffreys AS, Ulmer CS, Oddone EZ, Bosworth HB, Yancy WS Jr, Allen KD. Prevalence of and characteristics associated with insomnia and obstructive sleep apnea among veterans with knee and hip osteoarthritis. BMC Musculoskelet Disord. 2018 Mar 9;19(1):79. doi: 10.1186/s12891-018-1993-y.
Results Reference
derived
PubMed Identifier
26720751
Citation
Allen KD, Yancy WS Jr, Bosworth HB, Coffman CJ, Jeffreys AS, Datta SK, McDuffie J, Strauss JL, Oddone EZ. A Combined Patient and Provider Intervention for Management of Osteoarthritis in Veterans: A Randomized Clinical Trial. Ann Intern Med. 2016 Jan 19;164(2):73-83. doi: 10.7326/M15-0378. Epub 2015 Dec 22.
Results Reference
derived
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Patient and Provider Interventions for Managing Osteoarthritis in Primary Care
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