Sari Fulden, Sudan Aran Azize, Alp Gülay
Department of Physiotherapy and Rehabilitation, Faculty of Physical Therapy and Rehabilitation, Bingöl University, Bingöl, Turkey.
Department of Occupational Health and Safety, Faculty of Health Sciences, Bingöl University, Bingöl, Turkey.
Assist Technol. 2025 May 4;37(3):220-228. doi: 10.1080/10400435.2025.2458260. Epub 2025 Jan 31.
The study aims to evaluate the effects of virtual reality (VR) programs on disease activity, central sensitization, kinesiophobia, body awareness, and pain catastrophizing in patients with fibromyalgia syndrome (FMS). Twenty-nine with FMS were randomized into the VR group or the control group (CG). FMS patients in the VR group were included in the VR-based relaxing treatment for 4 weeks, with one session per week. The progressive muscle relaxation technique and the breath-counting exercise were taught to participants in the CG. The Fibromyalgia Impact Questionnaire (FIQ), Central Sensitization Inventory Short-Form (CSI-SF), TAMPA, Pain Catastrophizing Scale (PCS), and Body Awareness Questionnaire (BAQ) were evaluated. Additionally, in the VR group, the Galvanic Skin Response (GSR), Simulator Sickness Questionnaire (SSQ), pain, stress, and exhaustion were assessed during each session. Post-treatment, the VR group showed significantly greater improvements than the CG in FIQ, CSI-SF, PCS, and BAQ ( < 0.05). Effect sizes in the VR group, except for TAMPA, ranged from large to very large (Cohen's d = 0.993-1.350). Although GSR scores decreased post-treatment, this reduction was not statistically significant ( > 0.05). Additionally, symptoms of SSQ, pain, stress, and exhaustion were notably reduced in the VR group. we recommend the widespread use of this innovative treatment approach in FMS patients.
该研究旨在评估虚拟现实(VR)程序对纤维肌痛综合征(FMS)患者的疾病活动、中枢敏化、运动恐惧、身体感知和疼痛灾难化的影响。29名FMS患者被随机分为VR组或对照组(CG)。VR组的FMS患者接受了为期4周的基于VR的放松治疗,每周一次。对照组的参与者学习了渐进性肌肉放松技术和呼吸计数练习。评估了纤维肌痛影响问卷(FIQ)、中枢敏化量表简表(CSI-SF)、坦帕运动恐惧量表(TAMPA)、疼痛灾难化量表(PCS)和身体感知问卷(BAQ)。此外,在VR组中,每次治疗期间还评估了皮肤电反应(GSR)、模拟器晕动症问卷(SSQ)、疼痛、压力和疲惫程度。治疗后,VR组在FIQ、CSI-SF、PCS和BAQ方面的改善明显大于对照组(<0.05)。VR组除TAMPA外的效应量范围从大到非常大(科恩d值=0.993-1.350)。虽然治疗后GSR评分有所下降,但这种下降没有统计学意义(>0.05)。此外,VR组的SSQ、疼痛、压力和疲惫症状明显减轻。我们建议在FMS患者中广泛使用这种创新的治疗方法。