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Sensorimotor Training Versus Resistance Training in Patients With Knee Osteoarthritis

Efficacy of a Sensorimotor Training in Patients With Knee Osteoarthritis: a Randomized Clinical Trial

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01529398
Enrollment
96
Registered
2012-02-08
Start date
2008-03-31
Completion date
2009-08-31
Last updated
2012-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Keywords

knee osteoarthritis, exercise therapy, resistance training, proprioception

Brief summary

People with knee osteoarthritis (OA) have functional instability and defective neuromuscular function, it was recently suggested that sensorimotor exercises may be important and needed to improve the effectiveness of training programs for these patients. This study objective was to compare the effectiveness of a supervised resistance muscular training (RT) versus sensorimotor training (SMT) for patients with Knee OA, on decrease of pain and functional improvement.

Interventions

OTHERSensorimotor training (SMT)

The group realized 16 weeks of sensorimotor training, twice a week, with duration of 30 minutes each session. The intervention included agility and coordination exercises, perturbation training and stretching exercises. Also, the participants received orientation about the knee osteoarthritis.

The group realized 16 weeks of resistance training for the quadriceps and hamstring muscles, twice a week, with duration of 30 minutes each session. The intervention included strength leg raises, simple quadriceps and hamstring strengthening with cuff weights realized in 3 sets of ten repetition maximum(10RM) for each muscle group. The group also realized stretching exercises for lower limbs and received orientation about the knee osteoarthritis.

OTHERControl group (CG)

Patients in this group also received information about knee osteoarthritis and realized the same warm-up and cool-down intervention realized in the interventional groups. During 16 weeks they went to the ambulatory twice a week to perform 5 minutes of stationary bicycle and 5 minutes of stretching exercises for lower limbs.

Sponsors

Federal University of São Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with tibiofemoral osteoarthritis; * Both genders; * Age\> 50 years \<75 years; * Completion of clinical and radiological criteria of the American College of Rheumatology (ACR) criteria for knee OA; * No physical activity in the previous 3 months; * Education level from the 4th grade of primary school.

Exclusion criteria

* uncontrolled hypertension; * decompensated diabetes mellitus; * uncontrolled thyroid diseases; * cardiorespiratory disease (ischemia, arrhythmia, chest pain, or exercise-induced bronchospasm), liver abnormalities; * Patients with grade IV functional limitation that needed devices to walk(Kellgren-Lawrence radiographic classification); * Patients in a period of sick leave by the INSS or any other related factor; * Other rheumatic diseases.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale of pain (VAS)16 weeks
Get Up and Go Test16 weeks

Secondary

MeasureTime frameDescription
isometric quadriceps strength16 weeks
Medical Outcomes Study Short Form (SF-36)16 weeksGeneric, patient-report measure designed to assess health-related quality of life, comprises 36 items divided into 8 subscales. 1. Physical Functioning 2. Role Limitations due to Physical Problems 3. General Health Perceptions 4. Vitality 5. Social Functioning 6. Role Limitations due to Emotional Problems 7. General Mental Health 8. Health Transition
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)16 weeks
Tinetti Test16 weeks
activities of daily living scale (ADLS)16 weeks
Berg Balance Test16 weeks
electromyographic analysis of quadriceps muscle (EMG)16 weeks

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026