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Collaborative Lifestyle Intervention Program in Knee Osteoarthritis Patients

The Collaborative Lifestyle Intervention Program in Knee Osteoarthritis Patients: CLIP-OA

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02835326
Acronym
CLIP-OA
Enrollment
227
Registered
2016-07-18
Start date
2016-10-31
Completion date
2022-04-30
Last updated
2022-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis

Keywords

Older Adults, Weight Loss, Exercise, Knee pain

Brief summary

The Collaborative Lifestyle Intervention Program in Knee OsteoArthritis Patients (CLIP-OA) compares a novel community-based exercise and dietary weight loss program to the Arthritis Foundation's Walk with Ease intervention on improved mobility in knee osteoarthritis (OA) patients.

Detailed description

Knee OA is a chronic, progressive, degenerative disease that affects over 20 million Americans, and is cited as the primary cause for activity restriction and physical disability in older adults. The joint damage and symptoms (i.e., pain, stiffness, and fatigue) accompanying symptomatic knee OA result in activity restriction, muscle atrophy, reduced quality of life and difficulty in performance of functional tasks. Despite the well-established benefits of the Arthritis Foundation's (AF) exercise programs, recent evidence suggests that lifestyle interventions combining Exercise and Dietary Weight Loss (EX+DWL) results in superior improvements in key clinical outcomes in older, overweight or obese knee OA patients. Primary Aim: To compare the effects of a novel community-based EX+DWL program to AF's Walk with Ease (WWE) EX intervention on improved mobility in knee osteoarthritis (OA) patients. Secondary Aim: To compare the cost effectiveness and effects of the EX+DWL and WWE interventions on weight loss, pain, and quality of life.

Interventions

BEHAVIORALExercise and Dietary Weight Loss

The EX+DWL intervention consists of group and individual exercise sessions, as well as, nutritional and dietary counseling. Bimonthly phone calls are made in the final year of the study to aid in maintenance of the program.

BEHAVIORALWalk with Ease

The WWE 6 week program consists of health education lectures on arthritis self-management, a walking exercise portion, and at- home strength exercises. Participants will complete two consecutive WWE programs. Monthly and bimonthly phone calls are made to participants in months 4-12 and 12-24, respectively, to aid in maintenance of the program.

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
National Institute on Aging (NIA)
CollaboratorNIH
Ohio State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Diagnosed with knee OA: physician documented radiographic tibiofemoral OA of one or both knees * Overweight or Obese: BMI \>25 and \<40 * Knee Pain and Risk for Mobility Disability: self-reported difficulty walking ¼ mile, climbing stairs, lifting or carrying groceries, or performing other household activities due to knee pain * Sedentary: sedentary lifestyle defined as currently participating \< 20 minutes of weekly structured moderate intensity exercise occurring in bouts \>10 min * Health Status: all participants must be free of severe heart or systemic disease that would make moderate intensity exercise participation unsafe * Age: \> 50 years of age * Stability of Residence: does not plan to move out of the Columbus metropolitan area for the duration of the study * Consents: willing to give an informed consent and sign a HIPPA authorization form; (9) Physician Consent: treating rheumatologist and primary care physician provide medical consent for participation * Agreeableness: willing to accept randomization and complete all assessment and intervention procedures

Exclusion criteria

* Health Status: any serious medical condition that precludes safe participation in an exercise program * Study Staff Judgment: Inability to complete the study protocol, in the opinion of the study staff, due to frailty, illness, or other reasons

Design outcomes

Primary

MeasureTime frameDescription
Mobility Disabilitybaseline up to 2 yearsThis will be assessed using the 400 meter walk test (400MWT), which is the time to complete 400m as quickly as possible (without running)

Secondary

MeasureTime frameDescription
Functional Battery and Limitationsbaseline up to 2 yearsStair-climb time (SCT) is a functional performance measure that involves ascending and descending a flight of 5 stairs as quickly as possible. Limitations will be assessed using the Pepper Assessment Tool for Disability.
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)baseline up to two yearsScale of 0 (none) to 4 (extreme) indicating the amount of difficulty they have experienced performing basic physical function tasks in the past 48 hours due to knee OA. The physical function subscale consists of 17 items that will be summed to produce a physical function score. Higher scores indicating poorer function
Rand Medical Outcomes Study 36-item Short Form Health Survey (SF-36)baseline up to two yearsHealth related quality of life survey consisting of mental and physical health with subscales of physical functioning, mental health, role-physical, role-emotional, bodily pain, general health, vitality, and social functioning
Anthropometric Batterybaseline up to 2 yearsBody weight and height are used to calculate Body Mass Index (BMI). Body composition will be assessed using DEXA scans.
Social Cognitive Process Measuresbaseline up to two yearsPhysical activity barriers self-efficacy scale, Satisfaction with function and appearance scale, Multiple exercise self-regulatory self-efficacy scale, the weight efficacy lifestyle questionnaire (WEL), goal commitment and goal difficulty, arthritis self-efficacy, and pain acceptance.
Change in physical activitybaseline up to two yearsPhysical activity will be assessed using the Community Healthy Activities Model Program For Seniors (CHAMPS) and Lifecorder EX Accelerometer
Cost effectivenessbaseline up to two yearsThe cost-effectiveness of the EX+DWL intervention compared to the WWE \[program will be calculated as the ratio of additional cost per participant per increment of effectiveness. Effectiveness is based on improvement in the 400 MWT and the Quality of Well-being Scale- Self Administered (to calculate the Quality Adjusted Life Years).
Dietary intakebaseline up to two yearsDietary intake will be assessed by a registered dietician using the Daily food record measure. One weekend and 2 weekdays will be assessed.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026