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临床试验/NCT07585305
NCT07585305招募中不适用

Comparative Effects of Blood Flow Restriction Resistance Training Versus Blood Flow Restriction Cycling on Pain, Quadriceps Strength, and Functional Outcomes in Athletes With Patellofemoral Pain: A Randomized Controlled Trial

Ibadat International University, Islamabad1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2026年5月10日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
48
试验地点
1

研究概览

简要总结

This randomized controlled trial compares blood flow restriction (BFR) resistance training (leg press and seated knee extension at 30% 1RM) versus BFR cycling (stationary cycling at low resistance) in 60 athletes (aged 18-40 years) diagnosed with patellofemoral pain syndrome. Both interventions are delivered over 8 weeks (3 sessions/week) with a pneumatic cuff set at 80% limb occlusion pressure. Primary outcomes include pain intensity (NPRS), quadriceps strength (handheld dynamometer), and functional ability (Kujala Anterior Knee Pain Scale), assessed at baseline and post-intervention.

详细描述

Patellofemoral pain (PFP) is among the most prevalent musculoskeletal conditions in athletes, with reported prevalence of 30-40% in sports populations. High-load resistance training is the conventional rehabilitation approach but often exacerbates joint stress and reduces adherence. Blood flow restriction (BFR) training enables strength gains at low loads by applying a pneumatic cuff at 80% LOP on the proximal thigh.

This trial compares two BFR modalities:

  • Group A (BFR-RT): Leg press and seated knee extension, 1x30 + 3x15 reps at 30% 1RM, 3x/week for 8 weeks.
  • Group B (BFR-CYC): Stationary cycling at low resistance, 4x5-minute intervals at 70-80 RPM (RPE 11-13), 3x/week for 8 weeks.

All sessions are supervised one-on-one by a physiotherapist. Assessments are conducted at baseline and week 8. The study is single-blinded (outcome assessor blinded). Randomization via computer-generated sequence. Statistical analysis via SPSS v27 (paired t-test / Wilcoxon for within-group; independent t-test / Mann-Whitney for between-group, alpha=0.05).

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
Single (Outcomes Assessor)

盲法说明

This is a single-blinded study in which the outcome assessor is blinded to group allocation. Participants and treating physiotherapists are aware of the assigned intervention due to the nature of exercise-based rehabilitation. Efforts are made to standardize instructions and interaction across both groups to minimize bias.

入排标准

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

入选标准

  • Male and female athletes aged 18-40 years
  • Clinically diagnosed with patellofemoral pain syndrome
  • Anterior or retropatellar knee pain of at least 3 months duration
  • Pain provoked by at least two functional activities (e.g., squatting, stair climbing, running, prolonged sitting)
  • Willingness to participate and provide written informed consent

排除标准

  • History of knee surgery or significant knee trauma in the past 6 months
  • Presence of ligament, meniscal, or cartilage injuries
  • Neurological, vascular, or systemic inflammatory conditions
  • Contraindications to BFR training (e.g., deep vein thrombosis, uncontrolled hypertension)

研究组 & 干预措施

BFR Resistance Training Group

Active Comparator

Participants perform leg press and seated knee extension exercises at 30% of 1RM with a pneumatic cuff (12 cm wide, Delfi Medical) applied to the proximal thigh at 80% limb occlusion pressure (LOP). Protocol: 1 set of 30 + 3 sets of 15 repetitions, with 60-second rest between sets (cuff deflated). Frequency: 3 sessions/week for 8 weeks (24 sessions total). 1RM re-estimated every 2 weeks for progressive load adjustment. Warm-up: 10 min low-resistance cycling (no BFR). Cool-down: 5 min lower-limb stretching.

干预措施: Blood Flow Restriction Resistance Training (Device)

BFR Cycling Group

Experimental

Participants perform stationary cycling at low resistance targeting RPE 11-13, with a pneumatic cuff (12 cm wide, Delfi Medical) applied to the proximal thigh at 80% LOP. Protocol: 4 x 5-minute cycling intervals at 70-80 RPM, with 1-minute rest between intervals (cuff deflated). Frequency: 3 sessions/week for 8 weeks (24 sessions total). Cadence increased by 5 RPM if RPE <11. Warm-up: 10 min low-resistance cycling (no BFR). Cool-down: 5 min lower-limb stretching.

干预措施: Blood Flow Restriction Cycling (Device)

研究者

发起方
Ibadat International University, Islamabad
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hafsah Gul Khattak

Assistant Professor

Ibadat International University, Islamabad

研究点 (1)

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