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Low Level Laser Intervention for Individuals With Knee Osteoarthritis

Not Applicable
Completed
Conditions
Osteoarthritis, Knee
Interventions
Device: Low level laser treatment
Registration Number
NCT04828252
Lead Sponsor
National Cheng-Kung University Hospital
Brief Summary

The purpose of this study was to investigate the intervention effects of low level laser for knee OA group

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
56
Inclusion Criteria
  • The severity of osteoarthritis was defined by the Kellgren-Lawrence system as grade 2 - grade 3
Exclusion Criteria
  • Uncontrolled hypertension
  • Malignant tumor
  • Skin cancer
  • Pregnant
  • Dysesthesia
  • Pacemaker inplement
  • Cognitive problem
  • Fall record within 6 months
  • Dysfunction of blood coagulation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
808nmLow level laser treatmentThe wavelength of this experimental group was 808nm, total power: 3.6W, 15 minutes a session, 3 times a week for 8 weeks
660nmLow level laser treatmentThe wavelength of this experimental group was 660nm, total power: 3.6W, 15 minutes a session, 3 times a week for 8 weeks
ControlLow level laser treatmentThe wavelength of control group, total power: 0.0072W, 15 minutes a session, 3 times a week for 8 weeks
Primary Outcome Measures
NameTimeMethod
Changes of muscular strength of thigh measured by handheld dynamometerBaseline and after treatment, 8 weeks intervention

Muscular strength of the knee extensor and flexor on both sides and will be normalized by the body weight of participants' (lb/kg)

Secondary Outcome Measures
NameTimeMethod
Changes of walking speed measured by the stop watchBaseline and after treatment, 8 weeks intervention

40-m walk test, participants are instructed to walk as fast as they could, investigator records the time they spend. (seconds)

Changes of stair climbing ability measured by the stop watchBaseline and after treatment, 8 weeks intervention

stair climbing test, participants are instructed to climb stairs with a total height of 180 cm as fast as they could, investigator records the time they spend. (seconds)

Changes of chair stand ability, the stop watch will be used to measure time and investigators count the time that participants completeBaseline and after treatment, 8 weeks intervention

sit-to-stand test, participants are instructed to repeat chair stand movement as fast as they could, investigator records the times they complete. (times)

Changes of dynamic balance ability measured by the stop watchBaseline and after treatment, 8 weeks intervention

timed UP\&Go test, participants are instructed to stand up from a chair and walk as fast as they could for 3 meters and back to the chair, investigator records the time they spend. (seconds)

Trial Locations

Locations (1)

Department of Physical Therapy, National Cheng-Kung University

🇨🇳

Tainan, Taiwan

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