Short-term and Intermediate-term Effects of Self-applied Joint Mobilization Versus Clinician-applied Joint Mobilization in Addition to Exercise in Patients With Knee Osteoarthritis: A Randomized Clinical Trial

NCT ID: NCT07020897

Last Updated: 2025-06-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-07-15

Study Completion Date

2026-11-30

Brief Summary

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The goal of this clinical trial is to learn if a combination of patient self-administered joint mobilization and exercise works to treat knee osteoarthritis in adults. The main questions it aims to answer are:

* Does self-administered joint mobilization improve the ability to perform regular daily activities?
* Does self-administered joint mobilization improve knee motion?
* Does self-administered joint mobilization improve hip strength?

Researchers will compare the program of self-administered joint mobilization to a joint mobilization administered by a physical therapist.

Participants will:

* Attend 8-12 physical therapy clinic visits over 6 - 8 weeks
* Perform home exercises
* Visit the clinic 6 months later for a brief check-up

Detailed Description

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This study will take place in the Outpatient Rehabilitation Clinic at Texas Health Resources (THR) in Plano, or in the Texas Health Sports Medicine Clinic in Allen.

Participants in this study will be asked to complete the same intake forms and questionnaires as any other physical therapy patient being seen for knee pain at all of the THR physical therapy clinics. These will include questions about health history, learning style, living situation, and goals for physical therapy treatment. One investigator will perform a physical therapy evaluation, including joint motion, muscle strength, and flexibility measurements, as well as functional testing.

For this study, we will measure one knee motion and one hip strength item and ask participants to complete a knee- specific questionnaire 3 times: on the initial evaluation visit, during the last visit of physical therapy, and during a 6-month follow-up visit.

After the initial evaluation visit, we will assign each participant into one of the two treatment groups, self-joint mobilization or joint mobilization performed by a physical therapist. Participants will be asked to attend 7 - 11 physical therapy treatment visits over 7-8 weeks for strength training exercises, flexibility exercises, joint mobilization, and a home exercise program. Each physical therapy visit, including the initial evaluation visit will last 45 minutes. Participants will be asked to track compliance with a home program and attend a follow-up appointment about 6 months after the initial evaluation. This follow-up visit will last about 30 minutes.

All appointments, except for the 6-month follow-up, will be structured and carried out as they would for any other patient receiving physical therapy for knee pain.

Conditions

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Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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Clinician-administered joint mobilization

In-clinic exercise-based physical therapy, home exercise program, and clinician-administered joint mobilization.

Group Type ACTIVE_COMPARATOR

Clinician-administered joint mobilization

Intervention Type OTHER

Tibiofemoral arthrokinematic extension joint mobilization and multidirectional patellofemoral mobilization applied by a physical therapist.

Exercise-based physical therapy

Intervention Type OTHER

In-clinic exercise-based physical therapy supervised by a physical therapist, with home exercises to be performed on days without a clinical visit.

Self-administered joint mobilization

In-clinic exercise-based physical therapy, home exercise program, and self-administered joint mobilization.

Group Type EXPERIMENTAL

Self-administered joint mobilization

Intervention Type OTHER

Tibiofemoral arthrokinematic extension joint mobilization and multidirectional patellofemoral mobilization applied by the research participant.

Exercise-based physical therapy

Intervention Type OTHER

In-clinic exercise-based physical therapy supervised by a physical therapist, with home exercises to be performed on days without a clinical visit.

Interventions

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Clinician-administered joint mobilization

Tibiofemoral arthrokinematic extension joint mobilization and multidirectional patellofemoral mobilization applied by a physical therapist.

Intervention Type OTHER

Self-administered joint mobilization

Tibiofemoral arthrokinematic extension joint mobilization and multidirectional patellofemoral mobilization applied by the research participant.

Intervention Type OTHER

Exercise-based physical therapy

In-clinic exercise-based physical therapy supervised by a physical therapist, with home exercises to be performed on days without a clinical visit.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Meets National Institute for Health and care Excellence (NICE) criteria for knee osteoarthritis:
* Age 45 years or older
* Movement-related knee pain
* No morning stiffness or morning stiffness \< 30 minutes
* Knee flexion contracture (kFC) at least 1cm, measured by heel-height
* Fluency in verbal and written English for completion of outcome measure and screening, and to take directions.
* Able to attend all study-related appointments

Exclusion Criteria

* Assistive device required for ambulation
* Systemic disease affecting joint function (diabetes, rheumatological disorders, etc)
* Previous lower extremity joint replacement
* Lower quarter surgery, injection, or therapy in the past year
* Other functionally-limiting physical impairment of the lower quarter
* Spine or lower extremity compensation claim (work, accident, etc)
Minimum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Texas Health Resources

OTHER

Sponsor Role collaborator

Texas Woman's University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Guy L Terry, MPT, PhD(c)

Role: PRINCIPAL_INVESTIGATOR

Texas Woman's University

Locations

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Texas Health Resources Sports Medicine Allen

Allen, Texas, United States

Site Status

Texas Health Resources Plano Presbyterian Outpatient Rehabilitation

Plano, Texas, United States

Site Status

Countries

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United States

Central Contacts

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Guy L Terry, MPT, PhD(c)

Role: CONTACT

972-939-6501

Facility Contacts

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Guy L Terry, MPT, PhD(c)

Role: primary

972-939-6501

Guy L Terry, MPT, PhD(c)

Role: primary

972-939-6501

Other Identifiers

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IRB-FY2025-156

Identifier Type: -

Identifier Source: org_study_id

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