Rehabilitation Unit, Department of Neurosciences, University of Padua, Via Giustiniani 3, 35128 Padua, Italy.
Department of Rheumatology, University of Padua, Via Giustiniani 2, 35128 Padua, Italy.
Biomed Res Int. 2014;2014:474029. doi: 10.1155/2014/474029. Epub 2014 Jan 29.
To propose a rehabilitation protocol able to produce immediate and long-term beneficial effects on level of disability and overall performance in ADLs.
Forty-one FM patients were randomized to an exercise and educational-behavioral programme group (experimental group, EG = 21) or to a control group (CG = 20). Each subject was evaluated before, at the end (T1), and after 6 months (T6) from the conclusion of the rehabilitation treatment using the Fibromyalgia Impact Questionnaire (FIQ), the visual analogue scale (VAS), the Health Assessment Questionnaire (HAQ), the fatigue severity scale (FSS), the 6-minute walking test (6MWT), tender points count (TPC), and spinal active range of motion. The exercise protocol included 20 sessions consisting in self-awareness, stretching, strengthening, spine flexibility, and aerobic exercises, which patients were subsequently educated to perform at home.
The two groups were comparable at baseline. At T1, the EG showed a positive trend in FIQ, VAS, HAQ, and FSS scales and significant improvement in 6MWT and in most spinal active range of motion measurements (P between 0.001 and 0.04). The positive results were maintained at the follow-up.
The proposed programme was well tolerated and produced immediate and medium-term beneficial effects improving function and strain endurance. This trial is registered with DRKS00005071 on DRKS.
提出一个康复方案,能够对 ADL 中的残疾水平和整体表现产生即时和长期的有益影响。
41 名纤维肌痛患者被随机分配到运动和教育行为方案组(实验组,EG=21)或对照组(CG=20)。每个受试者在康复治疗结束前(T1)、结束时(T1)和结束后 6 个月(T6)进行评估,使用纤维肌痛影响问卷(FIQ)、视觉模拟量表(VAS)、健康评估问卷(HAQ)、疲劳严重程度量表(FSS)、6 分钟步行测试(6MWT)、压痛点数(TPC)和脊柱主动活动范围。运动方案包括 20 节课程,包括自我意识、伸展、力量训练、脊柱灵活性和有氧运动,患者随后接受在家中进行这些运动的教育。
两组在基线时具有可比性。在 T1 时,EG 在 FIQ、VAS、HAQ 和 FSS 量表上表现出积极趋势,在 6MWT 和大多数脊柱主动活动范围测量上有显著改善(P 值在 0.001 到 0.04 之间)。积极的结果在随访中得到维持。
所提出的方案耐受性良好,产生了即时和中期的有益效果,改善了功能和应变耐力。该试验在 DRKS 上以 DRKS00005071 号注册。