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The Effects of Home-Based Rehabilitation Treatments Among Persons With Symptomatic Knee Osteoarthritis

The Effects of Home-Based Rehabilitation Treatments Among Persons With Symptomatic Knee Osteoarthritis.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00735098
Enrollment
44
Registered
2008-08-14
Start date
2009-01-31
Completion date
2012-12-31
Last updated
2013-02-06

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

Conditions

Osteoarthritis

Keywords

Knee Osteoarthritis, arthritis

Brief summary

Knee Osteoarthritis (OA) is one of the most frequent causes of physical disability and pain among adults. Recent evidence suggests that shorter exercise programs that incorporate kinesthesia, balance and agility (KBA) techniques may result in more rapid symptom relief and functional improvements in comparison to traditional therapeutic exercise. KBA techniques are designed to improve dynamic joint stability by using a series of activities which challenge balance and coordination. To determine the independent effects of KBA training on functional abilities, it is necessary to test it as a training program unto itself. The proposed clinical trial is designed to do this by using three training groups: KBA only; lower extremity strength training only; and a combination of the two. The total exercise time and intensity of each condition will be approximately equal. A non-exercise group will control for any effects related to the testing procedures and the passage of time. Community volunteer men and women age 50 and over with physician diagnosed symptomatic knee OA will participate.

Interventions

OTHERKBA exercise

KBA exercise protocol, 3 times per week for 8 weeks

strength training exercise, 3 times per week for 8 weeks

OTHERKBA and strength training

KBA and strength training exercise, 3 times per week for 8 weeks

OTHERControl group

8 week control group

Sponsors

University of Zululand
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 50 years or over of either gender * Self-reported knee pain * Physician diagnosed tibiofemoral OA, unilateral or bilateral, per ACR guidelines * Demonstrated minimal knee OA related dysfunction per WOMAC score * Not engaged in a regular leg exercise program for minimum of 6 months

Exclusion criteria

* High risk health status per (e.g.) ACSM guidelines * Inability to obtain physician release for exercise * Unresolved balance disorder * Unresolved neurological disorder * History of knee surgery or major knee trauma injury * Hip or ankle instability, excessive weakness, surgery or major trauma injury * Hip or knee replacement * Intra-articular joint injection within 4 weeks of the study

Design outcomes

Primary

MeasureTime frame
(WOMAC) self assessment of physical function8 weeks

Countries

United States

Outcome results

None listed

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