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Effects of TENS During the Performance of a Therapeutic Exercise Protocol in Individuals With Knee Osteoarthritis.

Key facts

Where
São Paulo, BrazilSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 40 and 75 years old?

Source: NCT06184451, who can take part

Where in Brazil

  • Nove de Julho UniversitySão Paulo, BrazilContact: Cid GomesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
University of Nove de Julho
Trial code
NCT06184451
Record updated
8 October 2024
Original description
Research participants diagnosed with knee Osteoarthritis will be randomized through a draw using sealed opaque envelopes indicating two groups: 1. Therapeutic Exercises + Transcutaneous electrical nerve stimulation and 2. Therapeutic Exercises + placebo Transcutaneous electrical nerve stimulation.Read full original descriptionShow less

Effects of TENS During the Performance of a Therapeutic Exercise Protocol in Individuals With Knee Osteoarthritis: Controlled, Randomized, and Blinded Clinical Trial

Research participants diagnosed with knee Osteoarthritis will be randomized through a draw using sealed opaque envelopes indicating two groups: 1. Therapeutic Exercises + Transcutaneous electrical nerve stimulation and 2. Therapeutic Exercises + placebo Transcutaneous electrical nerve stimulation.

Therefore, individuals of both sexes, aged 40 years or over, with a clinical diagnosis of unilateral osteoarthritis of the knee, who present with knee pain for more than three months, morning stiffness for less than 30 minutes, crepitus, bone sensitivity and absence of palpable heat, and diagnosis established radiographically (determined by Kellgren and Lawrence grade 1 to 3 on scale 1 to 4).

Exclusion criteria are bilateral knee Osteoarthritis, hip Osteoarthritis, severe osteoporosis, fibromyalgia, clinical history of tumors or cancer, active inflammatory joint diseases (rheumatoid arthritis, gout), undergoing any lower extremity joint replacement, neurological disorders (Parkinson's disease, stroke, multiple sclerosis, muscular dystrophies, motor neuron disease, Alzheimer's disease), infected wounds or osteomyelitis in the knee region, deep vein thrombosis or thrombophlebitis, sensory changes in the lower limbs, cognitive impairment, and cardiopulmonary disorders that may prevent or limit the execution of exercises, use of a walking assistance device, history of recent trauma to the knee, having undergone any form of treatment involving physiotherapy, intra-articular corticosteroids, anti-inflammatories or chondroprotective within the six months before the start of interventions.

Inclusion: clinical diagnosis of unilateral osteoarthritis of the knee; presenting knee pain for more than three months; morning stiffness for less than 30 minutes; crepitus, bone tenderness, and absence of palpable heat.

Exclusion: intra-articular corticosteroids, anti-inflammatories, or chondroprotective in the six months before the start of the interventions; medical history of tumors or cancer; active inflammatory joint diseases (rheumatoid arthritis, gout),; neurological diseases (Parkinson's disease, Accident Cerebral Vascular, Multiple Sclerosis, muscular dystrophies, motor neuron disease, Alzheimer's disease); infected wounds or osteomyelitis in the knee region; deep vein thrombosis or thrombophlebitis; cognitive and cardiopulmonary impairment that may prevent or limit performing the exercises; having a history of recent trauma to the knee,; Bilateral knee osteoarthritis, hip osteoarthritis; severe osteoporosis; fibromyalgia; undergoing any lower extremity joint replacement; sensory changes in the lower limbs; using a walking assistance device; having undergone any form of treatment involving physiotherapy.

ClinicalTrials.gov NCT06184451