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Effectiveness of Simply Modified Walkers for Knee Osteoarthritis in Low-Income Settings: A Prospective Longitudinal Study.

The effect of the application of an innovative-technological walker with a power relief system for osteoarthritis patient

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20241011002
Enrollment
60
Registered
2024-10-11
Start date
2023-11-11
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

knee osteoarthritis knee osteoarthritis

Interventions

KOA participants using a modified walker in daily activities for 12 weeks.,KOA participants using a standard fix walker in daily activities for 12 weeks.,Individuals without knee osteoarthritis will r
Modified walker for KOA participants ,Standard walker for KOA participants ,No osteoarthritis participants

Sponsors

Research Grant of Burapha University through National Research Council of Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion Criteria 1. Volunteers with Osteoarthritis: 1.1 Male or female volunteers aged 45 years or older. 1.2 Diagnosed with knee osteoarthritis in at least one side 1.3 Able to walk 1.4 Use a walking aid in daily life, or a physiotherapist/physician deems it necessary to use a walking aid in daily life to reduce the risk of falling or to alleviate pain. 2. Volunteers without Osteoarthritis: 1. Male or female volunteers aged 45 years or older. 2. Never diagnosed with osteoarthritis in the lower extremity joints. 3. No lower extremity joint pain currently or in the month before joining the study. 4. Able to walk independently (without using walking aids).

Exclusion criteria

Exclusion criteria: 1. Unable to communicate for physical assessment. 2. Visual impairments that cannot be corrected with glasses, such as any type of cataracts or diabetic retinopathy. 3. Currently experiencing uncontrolled hypertension. 4. History of allergic reactions to the application of EMG electrodes. 5. High risk of adverse events during exercise. 6. Inability to consistently use a walker for 12 weeks (defined as more than 4 weeks of discontinuation of use, specific to volunteers with osteoarthritis).

Design outcomes

Primary

MeasureTime frame
muscle activation Before and 12 weeks after intervention surface EMG,Weight-Bearing Before and 12 weeks after intervention Four Force Plates DFP4 Dual Axis Weight-Bearing Evaluation ,Biomarker Before and 12 weeks after intervention Serum Biomarker,muscle morphology Before and 12 weeks after intervention Real time Ultrasound Imaging,knee extension-flexion strength Before and 12 weeks after intervention Biodex sytem 4Pro,cardiovascular response Before and 12 weeks after intervention Six-minute walk test,Functional lower limbs stregth Before and 12 weeks after intervention 5 sit to stand test,Knee Outcome Score Before and 12 weeks after intervention Knee Osteoarthritis Outcome Score (KOOS) ,Kinesiophobia Before and 12 weeks after intervention Tampa Scale for Kinesiophobia,Fear of fall Before and 12 weeks after intervention Falls Efficacy Scale,Physical Activity Before and 12 weeks after intervention Global Physical Activity Questionnaire: GPAQ,Pain Before and 12 weeks after intervention VAS for pain,Stress Before and 12 weeks after intervention Thai version of 10-Item Perceived Stress Scale-10 (T-PSS-10)

Secondary

MeasureTime frame
nerve conduction before and 12 weeks after intervention nerve conduction study,sarcopenia before and 12 weeks after intervention Asian Working Group for Sarcopenia; gait speed, calf circumference, Hand-grip strength, Body composition (InBody),satisfaction before and 12 weeks after intervention satisfaction score,Range of Motion before and 12 weeks after intervention Standard goniometer

Countries

Thailand

Contacts

Public ContactSIRIRAT KIATKULANUSORN

Burapa University

siriratk@go.buu.ac.th0882302582

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026