Low Level Laser Intervention for Individuals With Knee Osteoarthritis
- 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
- The severity of osteoarthritis was defined by the Kellgren-Lawrence system as grade 2 - grade 3
- 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
Group Intervention Description 808nm Low level laser treatment The wavelength of this experimental group was 808nm, total power: 3.6W, 15 minutes a session, 3 times a week for 8 weeks 660nm Low level laser treatment The wavelength of this experimental group was 660nm, total power: 3.6W, 15 minutes a session, 3 times a week for 8 weeks Control Low level laser treatment The wavelength of control group, total power: 0.0072W, 15 minutes a session, 3 times a week for 8 weeks
- Primary Outcome Measures
Name Time Method Changes of muscular strength of thigh measured by handheld dynamometer Baseline 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
Name Time Method Changes of walking speed measured by the stop watch Baseline 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 watch Baseline 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 complete Baseline 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 watch Baseline 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