Sarcopenia: revised European consensus on definition and diagnosis.
Alfonso J Cruz-Jentoft, Gülistan Bahat, Jürgen Bauer...
https://pubmed.ncbi.nlm.nih.gov/30312372Actively Recruiting
Led by Ankara Etlik City Hospital · Updated on 2025-09-16
62
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the effects of low-level laser therapy (LLLT) combined with a conventional home-based exercise program in adults over 50 years old who have knee osteoarthritis. This single-center, prospective, randomized controlled study aims to compare LLLT plus exercise versus exercise alone and to assess impacts on clinical outcomes, femoral cartilage thickness, quadriceps muscle thickness, and regional sarcopenia. The study includes patients with moderate knee osteoarthritis classified by standard criteria. Participants are randomly assigned to one of two groups. Both groups follow a 12-week home exercise program involving range of motion, stretching, relaxation, strengthening, and aerobic walking exercises. The LLLT group receives additional laser treatment five times a week for two weeks using a BTL SMART 4000 device at a wavelength of 835 nm and a dose of 10 J per point applied to six points around the knee. If LLLT proves superior, the exercise-only group may later receive the laser therapy. Before treatment and at one and three months after starting treatment, patients undergo evaluations including body measurements, ultrasound assessments of femoral cartilage and quadriceps thickness, the Sonographic Thigh Adjustment Ratio (STAR), muscle strength and function tests, pain levels using the Visual Analog Scale (VAS), the Western Ontario and McMaster Universities Arthritis Index (WOMAC), and quality of life via the SF-36 questionnaire. Weekly phone calls during the first month and biweekly thereafter support adherence to the exercise program. The study concludes with comprehensive clinical and imaging assessments to measure treatment effects.
CONDITIONS
Low-Level Laser Therapy in Knee Osteoarthritis: Effects on Clinical Outcomes, Femoral Cartilage Thickness and Regional Sarcopenia
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 weeks
Participants receive a conventional home-based exercise program for 12 weeks. Those in the laser therapy group will also receive low-level laser therapy 5 sessions per week for 2 weeks.
Weekly phone calls during the first month, then every two weeks thereafter; 2 weeks of in-person laser therapy sessions for those in the laser group
Duration - 3 months
Participants are evaluated at the 1st and 3rd months after treatment initiation for clinical outcomes and muscle and cartilage measurements.
2 visits (in-person) at 1 month and 3 months post-treatment
Total: 1 location
1
Ankara Etlik City Hospital
Ankara, YENIMAHALLE, Turkey (Türkiye), 06170
Actively Recruiting
I
IREM ADIGUZEL, MEDİCAL DOCTOR
O
OZGUR Z KARAAHMET, MEDİCAL DOCTOR
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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