Clinical trial

Healthy Living After Knee Replacement

Active, not recruiting · Not applicable · 1 countries · Registry ID NCT05190666

Active, not recruitingNot applicableInterventional

What this study is about

The purpose of this study is to examine if a weight loss program designed for adults after knee replacement improves weight loss, physical activity, pain, and function, as well as if the program is cost effective, as compared to a chronic disease self-management program.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

AgeNot listed to Not listed
SexAll
Healthy volunteersAccepted
ConditionArthroplasty, Overweight and Obesity

Full registry criteria

Inclusion Criteria: Participants must: * have a body mass index between 25-45 kg/m2 * have had a knee replacement (including primary, staged or independent bilateral, or revision) \<6 months prior to baseline assessment * have a computer, tablet, or smartphone with active internet access to self-monitor online and/or have a device or computer compatible with Fitbit * completion of baseline assessment measures (height, weight, function tests, surveys, ≥4 days valid of activity monitoring, and 1 day of dietary recall) * be English-speaking and able to read consent and study materials written in English * be willing to attend 4 in-person assessments. Exclusion Criteria: * have any contraindications to diet or weight loss * undergo simultaneous bilateral knee replacement or have a scheduled or anticipated knee replacement for the contralateral knee within the next 18 months * have a mobility limiting comorbidity unrelated to knee replacement (e.g. spinal stenosis, fibromyalgia, peripheral vascular disease, stroke) * are taking anti-obesity medications * are enrolled in a formal weight loss program * had or are planning to have bariatric/gastric/lap band surgery * are planning to relocate out of the Columbia or Greenville, SC areas in the next 18 months.

Treatments and study arms

PACE Weight Loss program

Behavioral

12 month phone-based behavioral weight loss program

Chronic Disease Self-Management

Behavioral

12 month phone-based chronic disease self-management program

Primary outcomes

Change in body weight at 6 months6 months

kg

Study locations

1 locations were listed when this page was built. The first 40 are shown.

University of South Carolina🇺🇸 Columbia, South Carolina, United States