JointADventure: A Worksite Activity-Diet Intervention for Chronic Knee Pain

Northwestern University

Status

Completed

Conditions

Chronic Knee Pain

Osteoarthritis, Knee

Treatments

Behavioral: A worksite activity-diet intervention

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT01977872

R21AR062317 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

JointADventure: A worksite activity-diet intervention for chronic knee pain is a randomized controlled trial evaluation of a physical activity and nutritional worksite intervention to decrease symptoms and disability associated with knee osteoarthritis (OA), a major public health problem and a leading cause of work disability and work absenteeism/presenteeism in the US workforce.

The overarching goal of this project is to find an effective and sustainable intervention strategy that can assist large populations of persons with or at risk for knee OA to attain and maintain healthy dietary and physical activity behaviors. This project has to potential to have a tremendous impact on improving symptoms and quality of life of persons with chronic knee pain and decreasing the functional limitation, work absenteeism/presenteeism, and soaring healthcare utilization associated with knee OA.

Full description

We will utilize a partnership with Blue Cross Blue Shield of Illinois (BCBSIL), a highly supportive wellness partner, with a strong history of investment in the health of its employees and subscribers. The combined Activity/Dietary (AD) intervention is administered by health professionals trained in motivational interviewing as healthy lifestyle coaches.

Over the first 6 months, the coaches provide:

individualized counseling based on a comprehensive assessment of baseline clinical, functional and behavioral factors that are barriers to healthy physical activity and dietary behaviors
group education, the content of which is modeled after the highly successful Diabetes Prevention Program physical activity/dietary intervention, and customized for those with knee symptoms.

Follow-up assessments continue for 6 additional months.

Specific aims are to:

assess the feasibility of conducting a randomized controlled trial of the JointADventure intervention at this worksite
estimate the effectiveness of the intervention to decrease body weight, improve dietary habits, and increase objectively-measured physical activity
to improve objectively measured functional performance
to improve self-reported arthritis-specific and generic health status and health utility

Enrollment

38 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

BCBSIL employee
Must be able to ambulate household distances (50 ft)
Must be able to read and speak English
Pain, aching, stiffness in or around one or both knees on most days for at least one month during the past 12 months
BMI of >25, but <40

Exclusion criteria

Primary diagnosis of fibromyalgia
Any co-morbidity that is more functionally limiting than the knee symptoms (e.g. spinal stenosis, peripheral vascular disease or residual effects of stroke)
Comorbid condition (based on medication review) that contraindicates a physical activity or dietary intervention
Total joint replacement surgery within 1 year or plans for total joint replacement in the next 12 months
Plans to relocate away from the Chicago-land area in the next 12 months
Being on a special diet that is inconsistent with the DASH diet
Concurrent involvement in a weight loss program