Actively Recruiting

Phase Not Applicable
Age: 40Years - 70Years
All Genders
Healthy Volunteers
ID07424352

Exploring the Benefits of Eccentric Training for Aging Adults With Knee Osteoarthritis

Led by University of Colorado, Denver · Updated on 2026-02-20

60

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

Sponsors

U

University of Colorado, Denver

Lead Sponsor

N

NIH/NCATS Colorado CTSA Grant Number T32TR004367

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether a new exercise program called eccentric overload training using a flywheel device can improve stair-climbing ability in people aged 40 to 70 with knee osteoarthritis. This study aims to see if this training, which challenges muscles during their lengthening phase, can enhance muscle structure, strength, and coordination better than usual methods. The goal is to improve stair movement safety and reduce fall risk by improving muscle quality and coordination. Participants will be divided into two groups. One group will complete an 8-week eccentric overload exercise program using a kBox flywheel device, with two to three sessions per week lasting 30 to 45 minutes. Exercises include squats, step-ups, and knee extensions to mimic stair climbing. After this, there will be an 8-week period without training for the initial group. The other group will maintain usual activity for 8 weeks, then complete the same 8-week exercise program. During the study, participants will undergo various assessments at baseline, 10 weeks, and 19 weeks. These include measures of stair-stepping smoothness, muscle health via ultrasound, strength tests, stair walking time, physical performance scores, joint movement analyses, and self-reported pain. The study will monitor how these outcomes change with training and detraining to understand the effects on muscle and movement in knee osteoarthritis.

CONDITIONS

Brief Title

Knee Osteoarthritis Rehabilitation Through Rotational Inertia

Who Can Participate

Age: 40Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 40 to 70 years
  • Radiographically confirmed knee osteoarthritis (Kellgren-Lawrence Grade 2 or 3)
  • Able to walk independently, with or without assistive devices
  • For healthy control group: aged 40 to 70 years, no radiographic knee osteoarthritis (KL Grade 0 or 1), no frequent knee pain, and no history of knee surgery, significant knee injury, or diagnosed knee conditions
Not Eligible

You will not qualify if you...

  • Uncontrolled hypertension or other cardiovascular disease
  • Musculoskeletal conditions preventing physical testing
  • Neurological muscle weakness such as from stroke or spinal cord injury
  • Body mass index over 34.9 kg/m²
  • Hospitalization within the past 3 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 8 weeks

Participants complete an 8-week eccentric overload resistance training program using a portable flywheel exercise device, performing two to three sessions per week focusing on functional lower-limb exercises like squats, step-ups, and knee extensions.

Two to three sessions per week, each lasting approximately 30 to 45 minutes

Detraining

Duration - 8 weeks

Participants cease the intervention and enter a detraining period to observe effects after stopping the exercise program.

No sessions; participants maintain usual activity

Delayed Treatment

Duration - 8 weeks

Participants initially maintaining usual activity begin the same 8-week eccentric overload resistance training using the flywheel device with two sessions per week.

Two sessions per week, each lasting approximately 30 to 45 minutes

Trial Site Locations

Total: 1 location

1

University of Colorado, Denver

Aurora, Colorado, United States, 80045

Actively Recruiting

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Research Team

K

Katie Boncella, MS

M

Michael Harris-Love, PT, MPT, DSc, FGSA, FAPTA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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