Physical Activity Pathway for Patients With Osteoarthritis in Primary Care (OA-PCP) (R33)

University of North Carolina, Chapel Hill240 enrolled

Overview

The purpose of this study is to test an osteoarthritis (OA) primary care Physical activity Care Pathway (OA-PCP), a scalable intervention that includes: 1) a practical process for physical inactivity screening in primary care, 2) a brief, tailored physical activity (PA) counseling intervention via telephone, 3) connection of patients with community programs and other resources to support PA, and 4) follow-up with patients to deliver additional appropriate counseling and referrals to PA resources. This program will be compared to another program that provides education on a variety of topics important to understanding osteoarthritis (OA) and its care.

This study will be a randomized pilot trial of the refined OA-PCP among n=240 patients age ≥65 with hip and/or knee OA recruited from primary care clinics. Participants will be assigned equally to either the OA-PCP or an attention control group. Participants will complete assessments at baseline, and 6-month and 12-month follow-up. Primary endpoint of the trial will be objectively assessed PA, measured via accelerometer and secondary endpoint will be self-reported pain and function.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

240

Conditions

Osteoarthritis

Interventions

OA-PCP InterventionBEHAVIORAL

The OA-PCP intervention includes brief physical activity (PA) counseling delivered via phone by a PA Coach trained in relevant aspects of PA and motivational interviewing. During the initial call, the PA Coach will ask participants about their current physical activity level and work with them to set physical activity goals. Then, after the first call, participants in this group will receive a call about two weeks later, then at about 3 months, 6 months, 9 months and 12 months later. During these calls, the PA coach will ask participants' about their progress toward PA goals and work with them to address any barriers or challenges. The coach will also help participants to identify any programs or resources that may help them to achieve their PA goals. Participants in this group will be asked to wear a wrist-worn monitor to help them track their PA during the intervention period. Also, if participants approve, the coach will use an online program to view their PA data.

Attention ControlBEHAVIORAL

This group will receive an intervention in the same "dose" (e.g., number and duration of phone calls and emails) as the OA-PCP group, but the content will not be PA-specific. During the first call, the Coach will discuss 2 topics, for which the amount of content parallels call #1 for the OA-PCP: What is OA? OA Diagnosis and OA Risk Factors. During the second call, the Coach will discuss the topic of Health Care Providers and Overview of OA Treatment Guidelines. Call topics for 3, 6, 9 and 12- month follow-up calls will be: Pain Medications, Mechanical Treatments (e.g., knee braces, footwear, joint protection), Complimentary and Alternative Therapies and discussion of OA and Mental Health, Sleep and Fatigue.

Eligibility

Sex: ALLMin age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age 65 or older * One other chronic health condition that qualified under Chronic Care Management (CCM) guidelines, including: diabetes, depression, hypertension, hyperlipidemia, heart failure, atrial fibrillation, ischemic heart disease, stroke/transient ischemic attack (TIA), peripheral vascular disease, Chronic obstructive pulmonary disease (COPD), bronchiectasis, asthma, rheumatoid arthritis, osteoarthritis, HIV/AIDS, chronic kidney disease, hepatitis (chronic \& viral B \& C) and osteoporosis * Current Joint Symptoms * Self-reported physical activity \<150 minutes per week * Willing to make a change in PA over the next 3 months Exclusion Criteria: * Pain in chest when performing physical activity * Pain in chest when not performing physical activity * Loss of balance because of dizziness or loss of consciousness * Recommendation from doctor to only perform physical activity under medical supervision * No documented diagnosis of knee or hip OA * Dementia or other memory loss condition * Active diagnosis of psychosis * Active Substance abuse disorder * Total knee or hip replacement surgery, meniscus tear, ligament tear, or other significant lower extremity injury or surgery in the last 6 months * Severe hearing or visual impairment * Serious/terminal illness as indicated by referral to hospice or palliative care * Unstable angina * Hospitalization for cardiovascular event in last 6 months * History of ventricular tachycardia * Unstable chronic obstructive pulmonary disease (2 hospitalizations within the previous 6 months and/or on oxygen) * Stroke with moderate to severe aphasia * Recent history (last 6 months) of three or more falls

Outcomes

Primary Outcomes

Change From Baseline to Month 6 in Objectively Assessed Physical Activity (Accelerometer)

Minutes of moderate to vigorous intensity physical activity (MVPA) per week measured via accelerometer

Time frame: Baseline, Month 6 (Follow-up)

Change From Baseline to Month 12 for Minutes in Objectively Assessed Physical Activity (Accelerometer)

Minutes of moderate to vigorous intensity physical activity (MVPA) per week measured via accelerometer

Time frame: Baseline, Month 12 (Follow-up)

Secondary Outcomes

Change From Baseline to Month 6 for Steps Per Day

Step counts measured via an accelerometer device.

Time frame: Baseline, Month 6 (Follow-up)

Change From Baseline to Month 12 for Steps Per Day

Step counts measured via an accelerometer device.

Time frame: Baseline, Month 12 (Follow-up)

Change From Baseline to Month 6 for Minutes of Sedentary Activity

Minutes of sedentary activity measured via an accelerometer device.

Time frame: Baseline, Month 6 (Follow-up)

Change From Baseline to Month 12 for Minutes of Sedentary Activity

Minutes of sedentary activity measured via an accelerometer device.

Time frame: Baseline, Month 12 (Follow-up)

Change From Baseline to Month 6 in Western Ontario and McMasters Universities Osteoarthritis (WOMAC) Function Subscale

The Western Ontario and McMasters Universities Osteoarthritis (WOMAC) function subscale includes 17 items rated on a Likert scale of 0 (no difficulty) to 4 (extreme difficulty), with ranges of 0-68 for the function subscale with higher scores indicating worse symptoms and function.

Time frame: Baseline, Month 6 (Follow-up)

Change From Baseline to Month 12 in Western Ontario and McMasters Universities Osteoarthritis (WOMAC) Function Subscale

Time frame: Baseline, Month 12 (Follow-up)

Change From Baseline to Month 6 in Western Ontario and McMasters Universities Osteoarthritis (WOMAC) Pain Subscale

The Western Ontario and McMasters Universities Osteoarthritis (WOMAC) Pain Subscale is a measure of lower extremity pain. It includes 5 items rated on a Likert scale of 0 (no pain) to 4 (extreme pain), with a total range of 0-20 with higher scores indicating worse symptoms and function.

Time frame: Baseline, Month 6 (Follow-up)

Change From Baseline to Month 12 in Western Ontario and McMasters Universities Osteoarthritis (WOMAC) Pain Subscale

Time frame: Baseline, Month 12 (Follow-up)

Physical Activity Pathway for Patients With Osteoarthritis in Primary Care (OA-PCP) (R33)

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes