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临床试验/NCT06187038
NCT06187038招募中不适用

Effects of Including a Chronic Pain Neuroscience Education Program for Individuals With Knee OA: Randomized, Blinded Clinical Trial

University of Nove de Julho1 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2024年5月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
92
试验地点
1
主要终点
Functional disability

研究概览

简要总结

Research participants diagnosed with knee osteoarthritis will be randomized through a draw using sealed opaque envelopes indicating two groups: 1. therapeutic exercises, 2. therapeutic exercises + chronic pain neuroscience education program. The primary outcome will be functional performance using a patient-reported measure, the Knee Injury and Osteoarthritis Outcome Score (KOOS).

The selected secondary outcomes will be pain intensity by the numerical pain scale (END), physical function reported by the patient by the patient-specific functional scale (EFEP), Pain self-efficacy questionnaire (PSEQ), functional mobility by the timed up and test (TUG), general effect perceived through the global perception scale (EPG), muscle strength through Maximum Voluntary Isometric Contraction (MVIC) and functionality and disability through the World Health Organization Disability Assessment Schedule (WHODAS).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A clinical diagnosis of knee osteoarthritis (knee pain for > 3 months
  • Morning stiffness <30 minutes
  • Bone tenderness, and absence of palpable heat and/or diagnosis established radiographically (determined by Kellgren and Lawrence grade 1 to 3 on a scale 1 up to 4)

排除标准

  • severe osteoporosis
  • Fibromyalgia
  • Medical history of tumors or cancer
  • Active inflammatory joint diseases (rheumatoid arthritis, gout)
  • Undergoing any lower extremity joint replacement
  • Neurological diseases (Parkinson's disease, stroke, Multiple Sclerosis, muscular dystrophy, motor neuron disease, Alzheimer's disease, cognitive and cardiopulmonary impairment that may prevent or limit the performance of exercises, use of a gait assistance device, history of recent knee trauma.
  • Having undergone any form of treatment involving physiotherapy, intra-articular corticosteroids, anti-inflammatories or chondroprotective in the last six months

研究组 & 干预措施

Therapeutic exercise group

Active Comparator

The therapeutic exercise program will include warm-up, resistance, neuromuscular, mobility, and balance exercises. Over ten weeks, two sessions of the therapeutic exercise program will be carried out individually, lasting approximately 60 minutes each-a total of 20 therapeutic exercise sessions. Therapeutic exercise sessions will be carried out at least 24 hours between sessions. The therapeutic exercises will be performed in up to three sets of 8-12 repetitions or 30-60 seconds each, with rest intervals of 90 seconds between sets.

干预措施: Therapeutic exercises (Other)

Therapeutic exercise group and pain neuroscience education program

Experimental

The therapeutic exercise program will include warm-up, resistance, neuromuscular, mobility, and balance exercises. Over ten weeks, two sessions of the therapeutic exercise program will be carried out individually, lasting approximately 60 minutes each-a total of 20 therapeutic exercise sessions. Therapeutic exercise sessions will be carried out at least 24 hours between sessions. The therapeutic exercises will be performed in up to three sets of 8-12 repetitions or 30-60 seconds each, with rest intervals of 90 seconds between sets. The chronic pain neuroscience education program will be based on three domains. Making sense of pain, exposure with control, and lifestyle changes.

干预措施: Therapeutic exercises (Other)

Therapeutic exercise group and pain neuroscience education program

Experimental

The therapeutic exercise program will include warm-up, resistance, neuromuscular, mobility, and balance exercises. Over ten weeks, two sessions of the therapeutic exercise program will be carried out individually, lasting approximately 60 minutes each-a total of 20 therapeutic exercise sessions. Therapeutic exercise sessions will be carried out at least 24 hours between sessions. The therapeutic exercises will be performed in up to three sets of 8-12 repetitions or 30-60 seconds each, with rest intervals of 90 seconds between sets. The chronic pain neuroscience education program will be based on three domains. Making sense of pain, exposure with control, and lifestyle changes.

干预措施: Therapeutic exercises + pain neuroscience education program (Other)

结局指标

主要结局

Functional disability

时间窗: Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.

Knee Injury and Osteoarthritis Outcome Score (KOOS). It aims to evaluate the domains of pain, symptoms, activities of daily living, function related to recreation and sports, and quality of life related to the knee. Totaling 42 items, each item must be answered using a Likert scale that ranges from 0 (best score) to 4 (worst score), and the score for each subscale ranges from 0 (worst score) to 100 (best score).

次要结局

  • Numerical Pain Scale(Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.)
  • Global Perception of Change scale(Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.)
  • Maximum voluntary isometric contraction(Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.)
  • Dynamic balance(Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.)
  • Functional self-perception(Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.)
  • Self-perceived functionality(Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.)
  • Functionality(Change from Baseline, after 10 weeks of intervention and 4 weeks after the end of the intervention.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Cid André Fidelis de Paula Gomes

Principal Investigator

University of Nove de Julho

研究点 (1)

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