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Clinical Trials/NCT07302204
NCT07302204
Not yet recruiting
Not Applicable

Efficacy of Aerobic Exercise Versus Therapeutic Exercises on Exercise-induced Hypoalgesia in Knee Osteoarthritis. Randomized Clinical Trial

University of Nove de Julho1 site in 1 country90 target enrollmentStarted: February 20, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
90
Locations
1
Primary Endpoint
Exercise-induced hypoalgesia (EIH)

Overview

Brief Summary

The study compares two exercise strategies in people with knee osteoarthritis. The first is aerobic exercise on a recumbent cycle ergometer, with effort controlled by the Borg scale. The second is a therapeutic exercise program with resistance, neuromuscular, mobility, and balance components. The primary objective is to determine which approach produces greater exercise induced hypoalgesia, measured by the increase in pressure pain threshold at the knee within the session across four anchor sessions during a ten week program. This is a randomized clinical trial with two parallel arms. Ninety participants, between forty five and seventy five years of age, will be allocated to one of the two groups. Allocation sequence concealment will be ensured using opaque envelopes. The outcome assessor will remain blinded to group allocation. The interventions will take place three times per week for ten weeks. Assessments will be performed at baseline and after ten weeks. Within session measurements will also be taken in weeks one, four, seven, and ten. The primary outcome is the intra session change in pressure pain threshold at the medial compartment of the knee. Secondary outcomes include exercise induced hypoalgesia in the quadriceps and trapezius, chronic adaptation of pressure pain threshold, conditioned pain modulation, pain intensity, pain self efficacy, knee related health status, functional performance, quadriceps strength, global perceived effect, and adherence. The planned sample size is forty five participants per group. The analysis will follow the intention to treat principle. The primary outcome will be compared using linear mixed models with group and time effects. Clinical outcomes at T1 will be adjusted for baseline values. Estimates, confidence intervals, and interpretation in light of minimally important differences will be reported.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
40 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Clinical diagnosis of symptomatic knee osteoarthritis for at least 3 months.
  • Report of knee pain for more than 3 months and average knee pain intensity ≥ 3 on the 0 to 10 Numeric Rating Scale.
  • Morning stiffness lasting less than 30 minutes.
  • Clinical signs compatible with knee osteoarthritis. crepitus, bony tenderness and absence of palpable warmth at the knee.

Exclusion Criteria

  • Signs and symptoms indicating the hip as the main source of pain.
  • Osteoporosis
  • Fibromyalgia
  • History of tumors or cancer
  • Active inflammatory joint diseases, such as rheumatoid arthritis or gout.
  • Previous arthroplasty of any lower limb joint.
  • Neurological diseases, including Parkinson's disease, stroke, multiple sclerosis, muscular dystrophy, motor neuron disease or Alzheimer's disease.
  • Cardiovascular diseases for which exercise is formally contraindicated.
  • Infected wounds or osteomyelitis in the knee region.
  • Deep vein thrombosis or thrombophlebitis.

Outcomes

Primary Outcomes

Exercise-induced hypoalgesia (EIH)

Time Frame: At weeks 1, 4, 7, and 10 of the 10 week intervention (within session, pre and immediately post exercise).

exercise induced hypoalgesia (EIH) of the medial compartment of the knees, measured by the change in pressure pain threshold (Δ PPT)

Secondary Outcomes

  • Exercise induced hypoalgesia of the quadriceps(Within session, immediately before and immediately after the exercise session at weeks 1, 4, 7, and 10 of the 10 week intervention.)
  • Exercise induced hypoalgesia of the upper trapezius(Within session, immediately before and immediately after the exercise session at weeks 1, 4, 7, and 10 of the 10 week intervention.)
  • Chronic adaptation of pressure pain threshold(Baseline and after 10 weeks of intervention.)
  • Conditioned pain modulation(Baseline and after 10 weeks of intervention.)
  • Pain intensity(Baseline and after 10 weeks of intervention.)
  • Pain self efficacy(Baseline and after 10 weeks of intervention.)
  • Knee related health status(Baseline and after 10 weeks of intervention.)
  • Patient specific functional status(Baseline and after 10 weeks of intervention.)
  • Functional performance, thirty second sit to stand test(Baseline and after 10 weeks of intervention.)
  • Quadriceps muscle strength(Baseline and after 10 weeks of intervention.)
  • Global perceived effect(After 10 weeks of intervention.)
  • Adherence to the intervention(Throughout the 10 week intervention period.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Cid André Fidelis de Paula Gomes

Professor Phd

University of Nove de Julho

Study Sites (1)

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