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临床试验/NCT07283237
NCT07283237进行中(未招募)不适用

Enhancing Medial Knee Pain Rehabilitation : A Clinical Trial On The Effectiveness Of Blood Flow Restriction In Combination With Targeted Exercises For Adult With Varus Deformity

Assiut University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年9月8日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
80
试验地点
1
主要终点
Oxford Knee Score (OKS)

研究概览

简要总结

Medial knee pain is common in active adults with varus knee alignment and can limit daily and sports activities. Standard physiotherapy can reduce pain and improve function, but strength gains may be suboptimal when patients cannot tolerate high loading due to pain. Blood flow restriction (BFR) training allows muscle strength and hypertrophy improvements at low external loads by partially restricting limb blood flow, thereby reducing joint stress. Although BFR has shown benefits in people with knee osteoarthritis, its effectiveness for medial knee pain associated with varus deformity is not well established.

This randomized controlled trial will investigate whether adding BFR to a targeted strengthening program provides superior outcomes compared with the same exercise program alone in active adults with medial knee pain and mild to moderate varus alignment. Approximately 80 participants aged 30-55 years with BMI 18-25, medial knee pain, Kellgren-Lawrence grade 1-3 osteoarthritis, and Hip-Knee-Ankle angle between >2° and ≤10° varus will be recruited from an outpatient setting. Participants will be randomly assigned (1:1) to either a specific exercise program (hip adductors/abductors, internal rotators, and knee extensors) or the same program performed with BFR using a pneumatic thigh cuff set at 40-80% limb occlusion pressure. Outcomes, including the Oxford Knee Score (primary), lower-extremity function, pain, quality of life, muscle strength, radiographic alignment, and relapse rates over 12 months, will be assessed at baseline and multiple follow-up points by blinded assessors.

详细描述

Medial knee pain in the presence of varus malalignment is a frequent clinical presentation in active adults and is strongly associated with increased medial compartment loading, progressive cartilage degeneration, and an elevated risk of symptomatic knee osteoarthritis. In patients with persistent symptoms and structural progression, realignment surgery such as high tibial osteotomy (HTO) is considered when the hip-knee-ankle (HKA) angle exceeds approximately 3° of varus and is often recommended at 5°-6° or more of symptomatic varus in relatively young, active individuals with preserved lateral compartment cartilage. In this context, mild, moderate, and severe varus deformities have been described in the literature as roughly 3°-5°, 6°-8°, and ≥9° of varus alignment, respectively. For many patients, however, there is a substantial window in which optimized conservative management could delay or possibly reduce the need for surgical realignment while improving pain and function.

Conventional physiotherapy and strengthening programs for medial knee pain and early knee osteoarthritis typically emphasize quadriceps and general lower-limb strengthening, flexibility, and neuromuscular training. These approaches can reduce pain and improve function but may not always achieve optimal muscle adaptation because patients often cannot tolerate high-load resistance exercise due to joint pain or fear of aggravating symptoms. As a result, clinicians are frequently constrained to suboptimal loading intensities, which may limit gains in strength and neuromuscular control that are needed to better support the varus knee and potentially reduce medial compartment load during everyday and sports activities.

Blood flow restriction (BFR) training has emerged as a promising adjunct in musculoskeletal rehabilitation, enabling meaningful improvements in muscle strength and hypertrophy at relatively low external loads. By applying a pneumatic cuff to partially restrict venous outflow while maintaining arterial inflow, BFR produces a metabolic and mechanical environment that mimics high-load training, but with considerably less joint stress. This is particularly relevant in populations with painful knee osteoarthritis or varus deformity, where high-load training is often poorly tolerated. Recent trials in knee osteoarthritis populations suggest that low-load BFR-enhanced exercise can lead to clinically important improvements in pain, muscle strength, and quality of life compared with similar exercise performed without BFR. However, the specific role of BFR in active adults with medial knee pain and varus malalignment has not been adequately explored.

This randomized controlled trial is designed to compare a targeted lower-limb strengthening and neuromuscular program alone with the same program combined with BFR in active adults with medial knee pain, mild to moderate varus deformity, and radiographic knee osteoarthritis (Kellgren-Lawrence grade 1-3). Eligible participants will be recruited from an outpatient physical therapy setting and will meet predefined clinical and radiographic criteria (detailed in the Eligibility section), including age range, body mass index, degree of varus malalignment on long-leg radiographs, and activity level. The sample size was determined a priori using G*Power to detect a moderate effect size in repeated-measures analyses with two groups and multiple time points, with additional allowance for attrition to yield an enrollment target of approximately 80 participants.

Participants will be allocated in a 1:1 ratio to either a control group receiving a specific exercise program or an experimental group performing the same exercises with the addition of BFR. The specific exercise program is designed to address key muscle groups that contribute to frontal-plane control and dynamic alignment of the lower limb, with a particular focus on the hip adductors, abductors, internal rotators, and knee extensors. Exercises will be delivered in a progressive manner over a 6-week supervised intervention period in the outpatient clinic, with standardized progression criteria and an accompanying home-exercise component to reinforce clinic-based training.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
30 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 30 and 55 years
  • Body Mass Index (BMI) between 18 and 25
  • Presence of medial knee pain
  • Mild to moderate varus deformity confirmed via X-Ray Long Film (2° < HKA ≤ 10°) (4)(4)(5)
  • Kellgren and Lawrence classification of osteoarthritis (grades 1-3) (6):
  • Grade 1 (doubtful): doubtful joint space narrowing and possible osteophytic lipping
  • Grade 2 (minimal): definite osteophytes and possible joint space narrowing
  • Grade 3 (moderate): moderate multiple osteophytes, definite narrowing of joint space, some sclerosis and possible deformity of bone ends
  • Active adults (based on REFA work classification)

排除标准

  • BMI > 25
  • History of knee surgery
  • Any contraindication to exercise or BFR, including:
  • History of deep vein thrombosis (DVT)
  • Uncontrolled hypertension
  • Peripheral vascular disease
  • Pregnancy
  • Other significant musculoskeletal or neurological conditions affecting lower extremity function (e.g., hip osteoarthritis, rheumatoid arthritis, peripheral neuropathy)

研究组 & 干预措施

Control Group - Targeted Exercise Program

Active Comparator

Participants in the control group will perform a specific targeted exercise program focusing on hip adductors, abductors, internal rotators, and knee extensors. Exercises will be performed at moderate intensity without any blood flow restriction. The program aims to improve lower limb alignment, muscle balance, and functional performance through conventional strengthening exercises.

干预措施: Targeted Exercise Program (Behavioral)

Intervention Group - Blood Flow Restriction (BFR) with Targeted Exercise Program

Experimental

Participants in the intervention group will perform the same targeted exercise program (hip adductors, abductors, internal rotators, and knee extensors) combined with Blood Flow Restriction (BFR) using a Smart Tools Plus (LLC, USA) pneumatic cuff applied to the proximal thigh.

Cuff pressure will be set individually at 40-80% of limb occlusion pressure (LOP), maintained during exercise sets and released during 1-minute rest intervals. The intervention aims to enhance muscle strength and function while minimizing joint stress and pain.

干预措施: Blood Flow Restriction (BFR) Training with Targeted Exercise Program (Device)

结局指标

主要结局

Oxford Knee Score (OKS)

时间窗: Baseline, 6 weeks (post-intervention), 3 months, and 6 months follow-up.

The Oxford Knee Score (OKS) is a validated 12-item questionnaire designed to assess knee function and pain during daily activities. Each item is scored from 0 to 4, with higher total scores indicating better knee function and reduced pain. It evaluates activities such as walking, climbing stairs, and rising from a chair, reflecting the participant's perceived level of recovery and functional ability.

次要结局

  • Lower Extremity Functional Scale (LEFS)(Baseline, 6 weeks, 3 months, and 6 months follow-up.)
  • Short Form-36 (SF-36) Quality of Life Questionnaire(Baseline, 6 weeks, 3 months, and 6 months follow-up.)
  • Numerical Pain Rating Scale (NPRS)(Baseline, 6 weeks, 3 months, and 6 months follow-up.)

研究者

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

Mariam ibrahim

Physical Therapy Research Fellow, Assiut University, EGYPT

Assiut University

研究点 (1)

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