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Anti-gravity Treadmill Training in Patients With Knee Osteoarthritis

G

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Status

Completed

Conditions

Knee Osteoarthritis

Treatments

Behavioral: Control
Behavioral: Conventional treadmill
Behavioral: Anti-gravity treadmill

Study type

Interventional

Funder types

Other

Identifiers

NCT05319964
E2-21-1004

Details and patient eligibility

About

The aim of this study is to compare anti-gravity treadmill training with traditional treadmill training in patients with moderate to severe knee osteoarthritis.

Full description

Patients with moderate to severe OA have persistent pain that significantly affects their functional status, activity participation, and quality of life. As with mild OA, non-pharmacological interventions that focus on education, exercise, and weight management are first-line treatments for patients with moderate to severe knee OA.

Exercise is recommended for all patients with moderate to severe knee OA to reduce pain and protect the joint. A meta-analysis showed that exercise has beneficial effects on pain, even in patients with severe disease and awaiting total knee replacement.Therefore, the objective of this study was to compare the effects of anti-gravity treadmill training and traditional treadmill training on pain levels, quality of life and functional capacity in patients with moderate and severe knee osteoarthritis.

In addition, it was aimed to compare the compliance of the patients to aerobic exercise.

Enrollment

30 patients

Sex

All

Ages

50 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female patients ≥ 50 and ≤ 75 years old
  • Patients with a diagnosis of knee OA in at least one knee according to the classification criteria of the American College of Rheumatology
  • Patients with Kellgren-Lawrence (K-L) knee OA staging III to IV
  • Patients reporting knee pain on most days of the past month
  • Patients with stable medical and psychological status
  • Patients willing to participate in the study

Exclusion criteria

Patients with serious cardiovascular, pulmonary, neurological disease or other musculoskeletal problems (inflammatory rheumatic disease, active synovitis, severe low back pain, hip/knee joint replacement or other hip/knee-related trauma, fracture, or surgery) that impair walking

  • Patients with a history of corticosteroid injection to the knee in the last 3 months
  • Patients who have received opioid analgesics or systemic corticosteroids in the last 3 months
  • Patients who have undergone any exercise program or physical therapy program for the lower extremities in the last 3 months
  • Patients with severe vision, hearing and language problems
  • Patients with a body mass index ≥35 kg /m²

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 3 patient groups

anti-gravity treadmill
Experimental group
Description:
Patients in all three study groups will receive hot pack, transcutaneous electrical nerve stimulation (TENS), therapeutic ultrasound 3 days a week for 8 weeks. Participants were provided 30 minutes anti-gravity treadmill sessions including a 5 minutes warm - up and cool - down period for each session, 3 days a week, for 8 weeks
Treatment:
Behavioral: Anti-gravity treadmill
conventional treadmill
Active Comparator group
Description:
Patients in all three study groups will receive hot pack, transcutaneous electrical nerve stimulation (TENS), therapeutic ultrasound, 3 days a week for 8 weeks. The moderate-intensity aerobic exercise program will be performed for 30 minutes at an intensity of 65-80% of the maximum heart rate, consisting of a 5-minute warm-up and cool-down period.
Treatment:
Behavioral: Conventional treadmill
Control
Other group
Description:
Patients in all three study groups will receive hot pack, transcutaneous electrical nerve stimulation (TENS), therapeutic ultrasound 3 days a week for 8 weeks
Treatment:
Behavioral: Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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