Actively Recruiting

Phase Not Applicable
Age: 45Years - 79Years
All Genders
NCT06857123

Feasibility of Resting Intervals During Exercise Programs for Individuals With Knee Osteoarthritis

Led by University of Pittsburgh · Updated on 2026-02-09

20

Participants Needed

1

Research Sites

108 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

C

Carnegie Mellon University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This pilot randomize trial tests the feasibility of administering two different exercise programs in people with knee osteoarthritis. One group receives the exercise program administered as usual, and the other group received the exercise program with resting intervals.

CONDITIONS

Official Title

Feasibility of Resting Intervals During Exercise Programs for Individuals With Knee Osteoarthritis

Who Can Participate

Age: 45Years - 79Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 45 and 79 years
  • Clinical diagnosis of primary, early to moderate stage knee osteoarthritis
  • Body mass index less than 35 kg/m2
  • Sedentary lifestyle
  • Knee joint is the most painful joint in the body
  • Ability to speak and understand English
  • Willingness to comply with all study procedures and be available for the duration of the study
Not Eligible

You will not qualify if you...

  • Non-osteoarthritis disease of the knee
  • Advanced knee osteoarthritis
  • Knee injection in the past 3 months
  • Major knee trauma or surgery in the past 5 years or previous knee surgery with hardware limiting cartilage assessment
  • Participation in regular exercise or physical activity
  • Participation in an intervention study for knee osteoarthritis
  • Currently using a cane, walker, or crutches to walk
  • History of cardiovascular disease or hypertension not controlled by medication
  • Two or more unexplained falls in the past year
  • Inflammatory, autoimmune, neurological, systemic, muscular, or connective tissue conditions affecting walking or exercise ability
  • Contraindication to MRI
  • Medical condition or characteristic that increases risk or prevents compliance with study procedures
  • Pregnant female
  • Acute or terminal illness

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

G

Gaupp

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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