Skip to content

Implementation of GLA:D Program in West Virginians With Osteoarthritis of the Knee

A Pilot Randomized Controlled Trial to Assess the Implementation and Outcomes of Good Life With Osteoarthritis (GLA:D) Program in West Virginians Suffering From the Osteoarthritis of the Knee

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04857879
Enrollment
24
Registered
2021-04-23
Start date
2021-08-06
Completion date
2022-07-31
Last updated
2021-09-05

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

Conditions

Osteoarthritis, Knee

Keywords

knee arthritis, Good Life with Osteoarthritis in Denmark, neuromuscular exercises

Brief summary

This study will examine feasibility of implementing Good Life with Osteoarthritis in Denmark (GLA:D) program in West Virginians with osteoarthritis of the knee

Detailed description

Using West Virginia (WV) as an implementation site, this study will examine the feasibility of process implementation and effectiveness of the Good Life with Osteoarthritis in Denmark (GLA:D) program in individuals with osteoarthritis of the knee (KOA). Specifically, the study will examine the feasibility and acceptability of the GLA:D program in individuals with KOA. This study will also assess the magnitude of changes in self-reported knee pain and functional impairments as well as physical performance in individuals who receive GLA:D compared to those who receive control interventions consisting of disease-specific education and exercises for KOA.

Interventions

OTHERGLA:D program (Good Life with osteoArthritis in Denmark)

GLA:D includes disease-specific education combined with neuromuscular exercises. Control interventions include disease-specific education combined with exercises to optimize movement and strength of the affected knee.

Sponsors

University of Toronto
CollaboratorOTHER
University of Southern Denmark
CollaboratorOTHER
Marshall University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
45 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Between 45 to 90 years of age, 2. Osteoarthritis of the knee (KOA) (Kellgren and Lawrence grade 2, 3, or 4) confirmed by an orthopedic surgeon based on plain film radiographs and symptoms, and 3. Recommendation by an orthopedic surgeon to pursue conservative management of KOA.

Exclusion criteria

1. Prior joint replacement surgery in the ipsilateral knee, 2. Known history of cognitive impairments or any neurodegenerative disease, 3. Any other neurological or musculoskeletal pathologies that have resulted in permanent mobility deficits or functional impairments, 4. Medical conditions that would preclude them from participating in exercise programs, and 5. Inability to read and comprehend English.

Design outcomes

Primary

MeasureTime frameDescription
Change in Knee injury and Osteoarthritis Outcome Score (KOOS4) scores from baseline to 12-weeks later12-weeksThe KOOS4 is a variant of full length KOOS that has all subscales of full length KOOS (pain, symptoms, ADL, and QOL) except sports and recreation activities subscale. There are 9 items in the pain subscale, 7 items in the symptom subscale, 17 items in the ADL subscale, and 4 items in the QOL subscale. The items across these subscales are scored on the scale of 0 to 4 where 0 indicates no problem and 4 indicates an extreme problem. Each subscale has sufficient stability and dimensionality, and therefore the score for each subscale is calculated independently on 0-100 interval with 0 indicating an extreme problem and 100 indicating no problems.

Countries

United States

Contacts

Primary ContactSaurabh P Mehta
mehtas@marshall.edu3046965620

Outcome results

None listed

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