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Digital Home-Exercise Therapy Application For Patients With Non-Surgical Knee Injuries

Efficacy of Digital Home-Exercise Therapy Application For Patients With Non-Surgical Knee Injuries: A Randomized, Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04323267
Enrollment
60
Registered
2020-03-26
Start date
2020-01-01
Completion date
2020-05-15
Last updated
2020-05-29

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

Conditions

Knee Injuries, Knee Osteoarthritis, Patellofemoral Syndrome

Keywords

knee pain, knee osteoarthritis, patellofemoral syndrome, physical therapy, digital health

Brief summary

Knee pain is one of the most prevalent musculoskeletal disorders in the United States. Conservative treatments generally consist of pharmacological agents and physical therapy. Unfortunately, such conservative care is often mismanaged, and little data is collected on clinical outcomes. The proposed investigation utilizes a novel and state-of-the-art mobile application (DETP) to guide an at-home exercise therapy program for non-operative knee pain. The purpose of this study is conducting a single-blind randomized, controlled, superiority study to compare the DETP to conventional physical therapy (PT). The investigators will seek to determine improvement in pain and function in PROMIS measures as the primary outcome. The investigators will also evaluate satisfaction with the application as a secondary outcome.

Interventions

DEVICELimber Digital Application

A mobile application was recently developed to address these needs. The application provides evidence-based, symptom specific home-exercise video programs for MSK conditions, as well as clinically-validated outcome measures for tracking progress.

BEHAVIORALPhysical therapy Therapy

Therapy prescription 2 x a week for 8 weeks (specified by physician)

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-75, inclusive. * Diagnosis of knee injury. For participants enrolled from the Mayo healthcare system database, knee injury identified from electronic medical records. * Pain Numerical Rating Scale score of 4 or greater on a 0-10 scale (0 = no pain, 10 = pain). * Participants must be diagnosed with a knee injury and the next step of care is either a home exercise program or external physical therapy ordered at the academic center. * Prescribed external physical therapy (i.e., therapy not completed at Mayo Clinic in Rochester/Minneapolis).

Exclusion criteria

* No access to android or iPhone smartphone * BMI greater than or equal to 35 * Previously completed series of physical therapy visits for knee injury within the past 12 months for the same injury (received one introduction PT session as seen in executive program will not be considered an exclusion). * Recommended by a physician for consideration of total knee replacement. * Diagnosis of rheumatoid arthritis, fibromyalgia, gout in the knee, or other systemic rheumatic disease. * Hospitalization for a stroke, heart attack, heart failure, or had surgery for blocked arteries in the past 12 months. * Total joint replacement knee surgery, bucket-handle meniscus tear, ACL tear, or other knee surgery in the past 12 months. * Unable to speak English. * Active diagnosis of psychosis. * Fall history deemed by a physician to impose risk for potential injury with participation in a home-based exercise program. * Severely impaired hearing or speech.

Design outcomes

Primary

MeasureTime frameDescription
PROMIS Pain Score8 weeksPain is measured by 0-100. 0 = no pain and 100 = very high pain
PROMIS Physical Function CAT8 weeksFunction is measured by 0-100. 0= no function and 100 = high function

Secondary

MeasureTime frameDescription
Subject Satisfaction Questions8 weeksSatisfaction questions

Countries

United States

Outcome results

None listed

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