Centre for Pain Research, School of Health, Leeds Beckett University, Leeds LS1 3HE, UK.
Research & Development Department, Airedale NHS Foundation Trust, Steeton, Keighley BD20 6TD, UK.
Medicina (Kaunas). 2022 Jun 14;58(6):803. doi: 10.3390/medicina58060803.
Background and Objectives: Characterising the features of methodologies, clinical attributes and intervention protocols, of studies is valuable to advise directions for research and practice. This article reports the findings of a secondary analysis of the features from studies screened as part of a large systematic review of TENS (the meta-TENS study). Materials and Methods: A descriptive analysis was performed on information associated with methodology, sample populations and intervention protocols from 381 randomised controlled trials (24,532 participants) evaluating TENS delivered at a strong comfortable intensity at the painful site in adults with pain, irrespective of diagnosis. Results: Studies were conducted in 43 countries commonly using parallel group design (n = 334) and one comparator group (n = 231). Mean ± standard deviation (SD) study sample size (64.05 ± 58.29 participants) and TENS group size (27.67 ± 21.90 participants) were small, with only 13 of 381 studies having 100 participants or more in the TENS group. Most TENS interventions were ‘high frequency’ (>10 pps, n = 276) and using 100 Hz (109/353 reports that stated a pulse frequency value). Of 476 comparator groups, 54.2% were active treatments (i.e., analgesic medication(s), exercise, manual therapies and electrophysical agents). Of 202 placebo comparator groups, 155 used a TENS device that did not deliver currents. At least 216 of 383 study groups were able to access other treatments whilst receiving TENS. Only 136 out of 381 reports included a statement about adverse events. Conclusions: Clinical studies on TENS are dominated by small parallel group evaluations of high frequency TENS that are often contaminated by concurrent treatment(s). Study reports tended focus on physiological and clinical implications rather than the veracity of methodology and findings. Previously published criteria for designing and reporting TENS studies were neglected and this should be corrected in future research using insights gleaned from this analysis.
对研究方法、临床特征和干预方案进行特征描述,有助于为研究和实践提供方向。本文报告了一项二次分析的结果,该分析对一项大型 TENS 系统评价(meta-TENS 研究)中筛选出的研究的特征进行了分析。
对 381 项随机对照试验(24532 名参与者)的方法、样本人群和干预方案信息进行描述性分析,这些研究评估了在疼痛部位给予强舒适强度的 TENS 对疼痛患者的效果,无论诊断如何。
研究在 43 个国家进行,通常采用平行组设计(n=334)和一个对照组(n=231)。平均(±标准差)研究样本量(64.05±58.29 名参与者)和 TENS 组样本量(27.67±21.90 名参与者)较小,只有 381 项研究中的 13 项 TENS 组有 100 名或更多参与者。大多数 TENS 干预措施为“高频”(>10pps,n=276),使用 100Hz(353 项报告中有 109 项报告了脉冲频率值)。在 476 个对照组中,54.2%为活性治疗(即镇痛药、运动、手法治疗和电物理治疗)。在 202 个安慰剂对照组中,155 个使用的 TENS 设备不输送电流。在接受 TENS 治疗的同时,至少有 216 个研究组能够接受其他治疗。在 381 份报告中,只有 136 份报告包含关于不良事件的声明。
TENS 的临床研究主要是高频 TENS 的小平行组评估,这些评估往往受到同时进行的治疗的影响。研究报告往往侧重于生理和临床意义,而不是方法和发现的真实性。先前发表的 TENS 研究设计和报告标准被忽视了,这应该在未来的研究中得到纠正,借鉴从本次分析中获得的见解。