Pavlou Kyriakos, Savva Christos, Korakakis Vasileios, Pamboris George M, Karagiannis Christos, Ploutarchou George, Constantinou Antonis
Department of Health Sciences, European University Cyprus, 1516 Nicosia, Cyprus.
Department of Health Sciences, Frederick University, 3080 Limassol, Cyprus.
Sports (Basel). 2023 Oct 9;11(10):197. doi: 10.3390/sports11100197.
"Nonspecific shoulder pain" encompasses various non-traumatic musculoskeletal shoulder disorders, diverging from diagnostic terminologies that refer to precise tissue-oriented clinical diagnosis. Blood flow restriction (BFR) training, involving partial arterial inflow and complete venous outflow restriction, has exhibited acute hypoalgesic effects primarily in healthy populations by increasing their pain thresholds. This study aims to examine whether a single BFR session with low-load exercises can alleviate pain perception among nonspecific shoulder pain patients. Conducted as a single-blind crossover randomised clinical trial, 48 adults (age range: 18 to 40) presenting with nonspecific shoulder pain will partake in two trial sessions. Random assignment will place participants into BFR or sham BFR groups and ask them to perform one exercise with BFR. Subsequently, participants will complete a shoulder girdle loading regimen comprising six exercises. The second session will involve participants switching treatment groups. Pain pressure thresholds (PPTs), shoulder pain and disability via the shoulder pain and disability index (SPADI), maximal voluntary isometric contraction (MVIC) of shoulder external rotators, pain during active abduction, and peak pain during shoulder external rotation will be evaluated using the numeric pain rating scale (NPRS). Immediate post-exercise assessments will include patient-perceived pain changes using the global rating of change scale (GROC) and participant-rated perceived exertion (RPE), employing a modified Borg's scale (Borg CR10) post-BFR or sham BFR exercise session. Each session will encompass three assessment periods, and a combination of mixed-effect models and descriptive statistics will underpin the analysis. This protocol was approved by Cyprus National Bioethics Committee (ΕΕΒΚ/2023/48), and was registered in ClinicalTrials.gov (Registration number: NCT05956288). Conclusion: The anticipated outcomes of this study illuminated the acute effects of BFR training on pain perception within the context of nonspecific shoulder pain, potentially advancing strategies for managing pain intensity using BFR techniques.
“非特异性肩痛”涵盖了各种非创伤性肌肉骨骼肩部疾病,与那些指精确的以组织为导向的临床诊断的诊断术语不同。血流限制(BFR)训练,包括部分动脉流入和完全静脉流出限制,主要通过提高健康人群的疼痛阈值,在他们身上展现出急性镇痛效果。本研究旨在检验一次低负荷运动的BFR训练能否减轻非特异性肩痛患者的疼痛感知。作为一项单盲交叉随机临床试验进行,48名患有非特异性肩痛的成年人(年龄范围:18至40岁)将参加两个试验阶段。随机分配将参与者分为BFR组或假BFR组,并要求他们在BFR状态下进行一项运动。随后,参与者将完成包括六项运动的肩带负荷方案。第二阶段将让参与者切换治疗组。将使用数字疼痛评分量表(NPRS)评估疼痛压力阈值(PPTs)、通过肩痛和功能障碍指数(SPADI)评估的肩部疼痛和功能障碍、肩外旋肌的最大自主等长收缩(MVIC)、主动外展时的疼痛以及肩外旋时的峰值疼痛。运动后立即评估将包括使用整体变化评分量表(GROC)评估患者感知的疼痛变化以及使用改良的Borg量表(Borg CR10)在BFR或假BFR运动训练后评估参与者评定的感知运动强度(RPE)。每个阶段将包括三个评估期,混合效应模型和描述性统计的组合将作为分析的基础。本方案已获得塞浦路斯国家生物伦理委员会(ΕΕΒΚ/2023/48)批准,并已在ClinicalTrials.gov上注册(注册号:NCT05956288)。结论:本研究的预期结果阐明了BFR训练在非特异性肩痛背景下对疼痛感知的急性影响,可能推进使用BFR技术管理疼痛强度的策略。