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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorIbadat International University, Islamabad

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

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)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Blood Flow Restriction Resistance Training

    Device

    Participants will undergo blood flow restriction (BFR) resistance training using a pneumatic cuff applied to the proximal thigh at 80% limb occlusion pressure. Exercises include leg press and seated knee extension performed at 30% of one-repetition maximum (1RM). Training will be conducted for 8 weeks, with supervised sessions 3 times per week. Cuff pressure will be monitored and adjusted using BP cuff. The aim is to improve quadriceps strength and reduce pain in patients with patellofemoral pain.

  • Blood Flow Restriction Cycling

    Device

    Participants will perform stationary cycling combined with blood flow restriction (BFR) applied to the proximal thigh at 80% limb occlusion pressure. Cycling will be performed at low resistance with controlled cadence for 8 weeks, 3 sessions per week under physiotherapist supervision. The protocol includes structured cycling intervals with rest periods and continuous monitoring of pain and perceived exertion. The intervention aims to improve quadriceps strength, reduce pain, and enhance functional outcomes in patients with patellofemoral pain.

Treatment groups

48 Participants
are divided into 2 treatment groups
Group A: BFR Resistance Training GroupActive comparator 1 intervention
Group B: BFR Cycling GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Quadriceps Strength - Handheld Dynamometer

Isometric quadriceps muscle strength measured in Newtons using a calibrated handheld dynamometer (ICC \> 0.90). Measurement taken in a standardized seated position at 60° knee flexion.

Time frame
Baseline (Week 0) and Post-intervention (Week 8)
2

Pain Intensity - Numeric Pain Rating Scale (NPRS)

Self-reported pain intensity rated on a 0-10 scale (0 = no pain, 10 = worst imaginable pain). The NPRS has excellent test-retest reliability (ICC 0.95).

Time frame
Baseline (Week 0) and Post-intervention (Week 8)

Secondary outcomes

1

Functional Outcomes - Kujala Anterior Knee Pain Scale (AKPS)

13-item patient-reported outcome measure assessing functional limitations due to anterior knee pain. Scored 0-100 (higher = better function). High internal consistency (α = 0.83-0.91).

Time frame
Baseline (Week 0) and Post-intervention (Week 8)

Other outcomes

Sponsors and contacts

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