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Moving Well for Total Knee Arthroplasty (TKA)

Moving Well Intervention for Patients Preparing to Undergo Total Knee Arthroplasty (TKA)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05217420
Enrollment
101
Registered
2022-02-01
Start date
2022-04-05
Completion date
2025-01-16
Last updated
2026-08-03

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

Conditions

Osteoarthritis, Knee

Keywords

arthroplasty, replacement, peer coach

Brief summary

The purpose of this study is to assess the efficacy of a behavioral intervention, Moving Well, in improving levels of anxiety and depression for patients undergoing total knee arthroplasty (TKA).

Detailed description

Moving Well is a behavioral intervention, guided by peer coaches, that aims to improve mental and physical preparation for patients planning to undergo total knee arthroplasty (TKA) and improve postoperative recovery and outcomes. Peer coaches are patients who themselves have had TKA due to advanced osteoarthritis (OA) of the knee and have been trained and certified to become peer coaches.

Interventions

BEHAVIORALMoving Well

Experimental arm

BEHAVIORALStaying Well

Active comparator arm

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER
Rheumatology Research Foundation
CollaboratorOTHER
Hospital for Special Surgery, New York
CollaboratorOTHER

Study design

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

Masking description

Only research team members who will collect objective in-person data will be masked

Eligibility

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

Inclusion criteria

* Subjects must have their primary TKR (one knee or both knees) scheduled in 8 weeks or more * Be willing to participate in the Moving Well (intervention) arm or Staying Well (attention control) arm * Are willing to work with a coach * ≥ 50 years of age * Speak English * Have access to the internet, computer, and a working phone * We will prioritize the recruitment of subjects with low socioeconomic status defined as being a beneficiary of Medicaid or no insurance and an underrepresented racial/ethnic group (Hispanic/Black).

Exclusion criteria

* Non-English speakers * The intervention will first be delivered in English to ensure feasibility with the content before adapting the material for patients who speak other languages. * TKR was a result of a septic joint or revision (implant malfunction) * Unable to exercise (e.g., bed bound or wheelchair bound) * Have had contralateral TKR or other joint replacement surgery (hip, shoulder) within the past 5 years * If they have RA or other connective tissue disease: Lupus, ankylosing spondylitis, psoriatic arthritis, scleroderma, infectious arthritis, polymyalgia rheumatica.

Design outcomes

Primary

MeasureTime frameDescription
Change in level of anxiety from baseline using the Generalized Anxiety Disorder Assessment (GAD-7)Baseline, 6 months post-surgeryThe GAD-7 is a 7 item self-reported questionnaire for screening and severity measuring of generalized anxiety disorder. Scores range from 0 to 21, with higher scores indicating greater severity of anxiety.
Change in level of depression from baseline using the Patient Health Questionnaire-8 (PHQ-8)Baseline, 6 months post-surgeryThe PHQ-8 is a 8 item scale that screens for depression. Scores range from 0 to 24 with higher scores indicating greater severity of depression.

Secondary

MeasureTime frameDescription
Change in level of social support from baseline using the Lubben Social Network Scale-18 (LSNS-18)Baseline, 6 months post-surgeryThe LSNS-18 is a 18 item scale that measures perceived social support. Scores range from 0 to 90 with higher scores indicating greater social engagement.
Change in general health status from baseline using the 12-Item Short Form Survey (SF-12)Baseline, 6 months post-surgeryThe SF-12 is a 12 item scale that assesses general health status. Scores range from 0 to 100 with higher scores indicating better physical and mental health functioning.
Change in level of pain catastrophizing from baseline using the Pain Catastrophizing Scale (PCS).Baseline, 6 months post-surgeryThe PCS is a 13 item scale that assesses the level of catastrophic thinking related to an individual's pain. Scores range from 0 to 52 with higher scores indicating a higher level of pain-related anxiety.
Change in level of knee pain and function from baseline using the Knee Injury and Osteoarthritis Outcome Score (KOOS) pain sub-scale.Baseline, 6 months post-surgeryThe KOOS pain sub-scale is a 9 item scale that assesses knee pain. Scores range from 0 to 100 with lower scores indicating greater severity of pain. The KOOS function sub-scale is a 17 item scale that assesses function. Scores range from 0 to 100 with lower scores indicating worse knee function.
Change in level of self-efficacy from baseline using the General Self-Efficacy Scale (GSF)Baseline, 6 months post-surgeryThe GSF is a 10 item scale that assesses perceived self-efficacy. Scores range from 10 to 40 with higher scores indicating a higher level of self-efficacy.
Change in sleep disturbance from baseline using the Patient-Reported Outcomes Information System (PROMIS) Sleep Disturbance Scale.Baseline, 6 months post-surgeryThe PROMIS Sleep Disturbance Scale is a 8 item scale that measure self-reported perceptions of sleep quality, depth, and restoration within the past seven days. Scores range from with higher scores indicating greater sleep disturbances.
Change in opioid use for knee pain from baseline using participant self-reportBaseline, 6 months post-surgerySelf-reported use of opioids for knee pain
Duration of post-surgery inpatient rehabilitation using the number of days of inpatient rehabilitation6 months post-surgerySelf-reported duration of inpatient rehabilitation
Change in knee range of motion from baseline using a goniometerBaseline, 6 months post-surgeryA goniometer measures the range of motion at a joint. Measurement ranges from 0 to 180 degrees with higher range indicating greater range of motion.
Change in Timed Up and Go test (TUG) from baselineBaseline, 6 months post-surgeryThe Timed Up and Go test is used to assess mobility. Completing the test in more than 12 seconds indicates a greater risk of falling in older adults.
Change in 6-minute walk test (6MWT) from baselineBaseline, 6 months post-surgeryThe 6MWT is used to assess aerobic capacity and endurance. The distance covered by walking for 6 minutes is measured and used to compare changes in performance capacity.
Change in 30-second chair to stand test from baselineBaseline, 6 months post-surgeryThe 30-second chair to stand test assesses leg strength and endurance. Scoring is based on the number of stands with a lower than average number indicating a greater risk of falls.
Change in quadriceps strength from baseline using a handheld dynamometer (HHD)Baseline, 6 months post-surgeryA handheld dynamometer is a device that measures muscle strength. Scores range from 0-300 pounds (upper limit can vary based on the device) with higher scores indicating greater quadriceps muscle strength.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORIris Y Navarro Millan, MD, MSPH

Weill Medical College of Cornell University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 4, 2026