Abstract

Background Stroke is ischemia and neurological dysfunction caused by acute brain circulation loss. It causes acute localized neurological abnormalities such as weakness, sensory deficit, or language issues that require long-term treatment. These deficiencies harm the patient and their family psychologically, socially, and economically. Thus, combination treatment can rapidly rehabilitate such patients. Detoxification methods like Ayurvedic medicated enema help stroke pathophysiology. Physical modalities in physiotherapy have been shown to facilitate normal movement and function on the stroke patient’s affected side, increasing independence with everyday duties. A stroke patient may benefit from Dashmoola Niruha Vasti, Function Electrical Stimulation (FES), and Motor Relearning Programme (MRP). Aim & Objectives This study compares the adjuvant role of Dashmoola Vasti with MRP and FES in stroke recovery. The main goals of this study are to assess and compare the adjuvant role of Dashmoola Vasti with standard control over sensorimotor function of lower extremities; static & dynamic balance in stroke patients; gait parameters; resistance experienced during passive range of motion; quality of life of patients; Barthel Index; Modified Ashworth Scale; and Fuglmeyer assessment, Single Limb Stance Test, Functional Reach Test. Methods A total of 40 patients will be enrolled and divided randomly into two equal groups. In Group A (control), standard treatment (modern + physiotherapy) will be prescribed for one month. In Group B (interventional group), Dashmoola Vasti will be added to the afore-said standard treatment for one month. Expected results Improvement in Fuglmeyer assessment, Single Limb Stance Test, Functional reach test, quality of life of patients, Barthel Index, Modified Ashworth scale and National Institute of Health (NIH) stroke-scale-score, will be observed and recorded. Conclusions Results and conclusions will be derived according to the data collected in case record form and assessment sheets filled at baseline and follow-up visits. Trial registration CTRI/2021/10/037445 dated 21.10.2021.

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