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Patient-Centered Weight Loss Program for Knee Replacement Patients

Patient-Centered Weight Loss Program for Knee Replacement Patients

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02728661
Acronym
PACE
Enrollment
16
Registered
2016-04-05
Start date
2016-05-31
Completion date
2017-06-30
Last updated
2023-10-26

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

Conditions

ARTHROPLASTY, REPLACEMENT

Brief summary

PACE is a patient-centered weight loss program that was developed specifically for knee replacements based on input from stakeholders, including knee replacement patients, physical therapists, and orthopedic surgeons. In this pilot study, participants undergoing knee replacement will be randomized to either start a weight loss program before surgery (PACE) or after surgery (Delayed PACE). Both programs will receive a 14-week intervention and complete assessments at baseline (up to 6 weeks prior to surgery), 12 weeks after surgery, and 26 weeks after surgery.

Detailed description

It is estimated that half of patients diagnosed with knee osteoarthritis (OA) will need a total knee replacement (TKR) during their lifetime. Of patients who need a TKR, 80-95% are overweight or obese. While patients are encouraged to lose weight, limited, if any, guidance is provided to achieve recommended weight loss. Many patients perceive that TKR is a necessary precursor for the initiation of weight loss. Yet, 66% of patients actually gain weight by 2 years after surgery. Patients undergoing TKR not only face unique barriers (i.e., pain, mobility limitations, motivation) to weight loss, but also have to balance pre- and post-operative concerns from physicians, surgeons, and rehabilitation specialists. To best accommodate the needs of both patients (pre- and post-TKR) and healthcare professionals (i.e., surgeon, physical therapist), patient and stakeholder engagement and activation is imperative in the development of a patient-centered weight loss intervention. Investigators completed 20 interviews with patients pre- and post-TKR and identified weight loss barriers, preferred intervention components (e.g., delivery method, contact frequency, self-monitoring modality) and patient-reported outcomes (e.g., physical function, pain) viewed as critical by patients. Investigators developed a patient-centered weight loss program (PACE) guided by these results and additional input from stakeholders to meet the needs of patients and healthcare professionals. PACE is a randomized pilot study comparing weight loss and patient-reported outcomes between PACE (program starting up to 6 weeks pre-TKR to 12 weeks post-TKR) and Delayed PACE (program starting 12 weeks post-TKR to 26 weeks post-TKR).

Interventions

BEHAVIORALPACE

PACE is an 14 week behavioral weight loss intervention developed specifically for knee replacement patients that starts up to 6 weeks prior to surgery.

BEHAVIORALDelayed PACE

Delayed PACE is an 14 week behavioral weight loss intervention developed specifically for knee replacement patients that starts 12 weeks after surgery.

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 79 Years
Healthy volunteers
No

Inclusion criteria

* BMI between 25-45 kg/m2 * Have a scheduled knee replacement at least 1 week away from baseline assessment * Obtain physician approval to participate * English speaking * willing to attend 3 in-person assessments.

Exclusion criteria

* Have any contraindications to diet or weight loss * Undergoing simultaneous bilateral knee replacement or have a scheduled or anticipated knee replacement for the contralateral knee in the next 26 weeks * Have a mobility limiting comorbidity besides relating to TKR * Taking anti-obesity medications * Enrolled in a formal weight loss program * Have had or is planning to have bariatric/gastric/lapband surgery * Is planning to relocate out of the Chicago land area in the next 12 months.

Design outcomes

Primary

MeasureTime frame
Change in weight measured with a balance-beam scaleChange from baseline to 12 and 26 weeks

Secondary

MeasureTime frame
Change in physical function assessed by the timed up and goChange from baseline to 12 and 26 weeks
Change in pain measured by WOMACChange from baseline to 12 and 26 weeks

Other

MeasureTime frame
Change in physical activity objectively-measured with accelerometryChange from baseline to 12 and 26 weeks
Behavioral adherence assessed by session and self-monitoring completion26 weeks post-op

Countries

United States

Outcome results

None listed

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