Key result
This paper describes the protocol for a randomized controlled trial evaluating transcutaneous vagal stimulation for pain reduction in knee osteoarthritis, and therefore reports no clinical results.
Why the study?
Current treatments for knee osteoarthritis are only partially effective, and evidence regarding the efficacy of transcutaneous vagal stimulation in knee osteoarthritis is lacking.
Does active transcutaneous vagal stimulation plus physical exercise reduce pain intensity in patients aged 55 years or older with knee osteoarthritis?
RCT (n=70)
Double-blind
randomly assigned
Does active transcutaneous vagal stimulation plus physical exercise reduce pain intensity in patients aged 55 years or older with knee osteoarthritis?
This trial protocol outlines a study to evaluate whether transcutaneous vagal stimulation combined with exercise can reduce pain in older adults with knee osteoarthritis.
Current treatments for knee osteoarthritis (KOA) are partially effective. It is, therefore, necessary to find new strategies that can complement the existing ones. In this scenario, transcutaneous vagal stimulation (TVS) neurophysiological effects could be a helpful solution. However, there is no evidence of the efficacy of TVS in KOA. This trial aims to assess the efficacy of TVS in decreasing pain in participants aged 55 years or older with KOA. A randomised controlled, two-arm, double-blind (participants and outcome assessors) and clinical superiority trial will be conducted for 70 patients with KOA. All the participants will carry out an exercise program. It consists of 12 sessions over four weeks. In addition, they will be randomly assigned to (1) active TVS plus physical exercise or (2) sham TVS plus physical exercise. The application of active TVS consists of electronic stimulation of the auricular concha using a portable device. Sham TVS condition consists of the stimulation of the earlobe that does not cause neurophysiological effects. The primary outcome is the reduction in pain intensity. Additionally, functional capacity, physical performance, pain-related interference, pain-related distress, quality of life in older adults and global change will be measured. Assessments will be conducted at the beginning of the study (baseline), at the end of the intervention and after 1 and 3 months of follow-up. This trial will generate evidence regarding the efficacy of TVS in pain perception in individuals with KOA. This information will serve as an input in the clinical decision-making on the use or non-use of TVS in individuals with KOA. Thus, if the efficacy of TVS is confirmed, a new therapeutic tool may be included in the rehabilitation of individuals with KOA.
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Bascour–Sandoval et al. (2022) conducted an RCT in Knee osteoarthritis (n=70). Transcutaneous vagal stimulation (TVS) plus physical exercise vs. Sham TVS plus physical exercise was evaluated on Reduction in pain intensity. This paper describes the protocol for a randomized controlled trial evaluating transcutaneous vagal stimulation for pain reduction in knee osteoarthritis, and therefore reports no clinical results.
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