Effectiveness of Low-Load Resistance Training With Blood Flow Restriction in Lateral Epicondylitis

This study aims to evaluate the effectiveness of low-load resistance training with blood flow restriction (LLRT-BFR) in patients with lateral epicondylitis using clinical and ultrasonographic assessments.

Patients aged 18-65 years who present to the Physical Medicine and Rehabilitation outpatient clinic at Sisli Hamidiye Etfal Training and Research Hospital with elbow pain lasting longer than 2 weeks and shorter than 12 weeks will be screened for eligibility. A clinical diagnosis of lateral epicondylitis will be established by a physician based on localized pain at the tenoperiosteal junction of the common extensor tendon (CET) at the lateral epicondyle (LE) and its surrounding area, tenderness on palpation, pain elicited by provocation tests, including resisted wrist extension and resisted third finger extension, reduced grip strength, and impairment in activities of daily living. Patients who meet the inclusion criteria and provide informed consent will be enrolled.

Eligible participants will be randomly allocated into two groups using a computerized randomization program, with stratification based on sex, age, and upper extremity dominance. These two groups will be an experimental group receiving low-load resistance training with blood flow restriction (LLRT-BFR) and a control group receiving the same low-load resistance training with sham blood flow restriction (LLRT-Sham BFR).

In the LLRT-BFR treatment group, individualized arterial occlusion pressure (AOP) will be determined prior to each session. A pneumatic cuff will be placed at the most proximal region of the upper extremity, just distal to the deltoid muscle insertion. During exercise, cuff pressure will be set at a standardized level corresponding to 40% of the measured AOP, in accordance with previously published protocols. Participants in this group will undergo supervised LLRT-BFR sessions twice weekly for 6 weeks, totaling 12 sessions.

In the LLRT-Sham BFR control group, individualized arterial occlusion pressure (AOP) will also be determined prior to each session. A pneumatic cuff will be placed at the most proximal region of the upper extremity, just distal to the deltoid muscle insertion, in the same manner as in the experimental group. During exercise, the cuff will be applied without intentional inflation; any pressure present will be limited to that resulting from cuff placement alone and will be substantially lower than the individually determined arterial occlusion pressure (AOP), and insufficient to induce meaningful blood flow restriction. Participants in this group will undergo supervised LLRT-Sham BFR sessions twice weekly for 6 weeks, totaling 12 sessions.

AOP will be assessed while the patient is seated comfortably, using a pneumatic cuff and Doppler ultrasonography with a linear ultrasound probe suitable for musculoskeletal examination to detect radial artery pulsation. Care will be taken to apply minimal probe pressure to avoid influencing AOP measurements. The cuff pressure at which Doppler activity due to radial artery pulsation is no longer detectable will be recorded as the AOP. During exercise, cuff pressure will be applied according to group allocation and maintained throughout each exercise set, and released between different exercises, allowing continued arterial inflow while temporarily restricting venous outflow in a controlled and safe manner.

Each treatment session will include approximately 45 minutes of supervised exercise therapy conducted in accordance with routine clinical practice. The exercise program will consist of low-load strengthening exercises for wrist flexion and extension, forearm pronation and supination, and wrist radial and ulnar deviation, as well as stretching exercises targeting the wrist flexor and extensor muscle groups. Exercises will be performed in a 3x10 repetition scheme, with 30-second rest intervals between sets and 90-second rest intervals between exercises targeting different muscle groups.

Clinical and ultrasonographic assessments will be conducted at baseline (pre-treatment), on the first day after treatment completion, and at 4 and 12 weeks post-treatment. The primary outcome measure will be functional status assessed using the Patient-Rated Tennis Elbow Evaluation (PRTEE) questionnaire. Secondary outcome measures will include pain intensity assessed by visual analog scale (VAS) during movement, at rest, at night, and during maximal grip; pain sensitivity assessed as pressure pain threshold using an algometer; maximal and pain-free grip strength assessed using a handheld dynamometer; ultrasonographic measurements of common extensor tendon thickness obtained at standardized anatomical locations (1 cm distal to the lateral epicondyle, capitellar region, and radiocapitellar region); cross-sectional area measurements of the extensor carpi radialis brevis and extensor digitorum communis muscles performed at a standardized level corresponding to 40% of the forearm length measured distally from the lateral epicondyle toward the Lister tubercle; the Total Ultrasonography Scale Score evaluating predefined tendon characteristics (e.g., hypoechogenicity, neovascularization, heterogeneity, and bony abnormalities); and treatment satisfaction assessed using the Roles-Maudsley Score.

The influence of demographic and anthropometric variables, including sex, age, height, weight, body mass index (BMI), and upper extremity dominance, on outcome measures will also be analyzed.

Randomization will be performed using a computerized randomization program by a non-evaluating research assistant who will be aware of group allocation and responsible for data recording. Blinding will be ensured by keeping participants unaware of their group assignment and by maintaining outcome assessors blinded to group allocation throughout the study. The study is designed as a single-center, prospective, randomized, double-blind, controlled clinical trial.