Application of Action Observation Therapy in Swallowing Rehabilitation: A Randomised Controlled Study

吞咽 神经康复 吞咽困难 生活质量(医疗保健) 医学 物理疗法 康复 贝克抑郁量表 物理医学与康复 萧条(经济学) 随机对照试验 显著性差异 咽肌 心理学 肌电图 手部力量 神经可塑性 功能训练
作者
A. Ucar,Bilge Piri Çınar,Banu Alıcıoğlu,Geylan BOSTAN,Sevil Bilgin
出处
期刊:Journal of Oral Rehabilitation [Wiley]
卷期号:52 (3): 320-331 被引量:1
标识
DOI:10.1111/joor.13902
摘要

ABSTRACT Background Action Observation Therapy (AOT) has emerged as a potential neurorehabilitation therapy to promote motor control for individuals with neurological dysphagia (ND), facilitating neural plasticity through activation of the mirror nervous system. Objective The aim of this study was to investigate the effect of AOT‐based dysphagia rehabilitation on suprahyoid (SH) muscle activation, swallowing difficulties, swallowing function, depressive symptom and quality of life in ND patients. Methods Thirty‐four participants with ND were randomly allocated to the AOT group ( n = 17) or control group ( n = 17). All participants underwent a 4‐week (5 sessions per week) conventional swallowing therapy. The AOT group watched exercise videos before doing these exercises, and the control group performed the same exercises without the videos. Surface electromyographic (sEMG) activation of suprahyoid muscles, Eating Assessment Tool 10 Turkish Version (T‐EAT 10) and Swallowing Ability and Function Evaluation (SAFE) for swallowing difficulties and swallowing function, Swallow Quality of Life Questionnaire (SWAL‐QOL) and Beck Depression Inventory (BDI) for quality of life and depressive symptom severity were evaluated. Results Post‐treatment SH amplitude level and T‐EAT‐10 scores were significantly lower in the AOT group compared to the control group ( p = 0.001, p = 0.012). There was a significant improvement in SAFE after treatment in the AOT group ( p < 0.05); however, there was no significant difference between the two groups ( p > 0.05). Both groups showed similar improvement in quality of life and depression. Conclusion This study showed that AOT can be a good option for improving the SH muscle activation and dysphagia difficulties in ND patients. Trial Registration ClinicalTrials.gov identifier: NCT05782790
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