EFFECT OF SUPER INDUCTIVE SYSTEM THERAPY COMBINED WITH MCIMT ON SPASTIC HAND IN STROKE PATIENTS– A SINGLE BLINDED, RANDOMIZED CONTROLLED TRIAL.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 16
- 试验地点
- 1
研究概览
简要总结
This study aims to investigate the effect of**Super Inductive System (SIS) therapy combined with modified Constraint-Induced Movement Therapy (mCIMT)**on hand spasticity and upper limb function in individuals with stroke. Post stroke spasticity is a common and disabling motor disorder that limits functional independence, reduces quality of life, and leads to secondary complications such as contractures, pain, and pressure sores. Although conventional physiotherapy, pharmacological management, and invasive procedures are available, they often provide only short term benefits or have limitations related to cost, accessibility, and adverse effects.
mCIMT is an evidence based intervention that promotes use of the affected limb through intensive task specific training and restraint of the unaffected limb, thereby enhancing neuroplasticity and functional recovery. However, its direct effect on spasticity is limited, especially in patients with marked hypertonia. SIS therapy is a recent, non invasive modality that uses high intensity electromagnetic stimulation to induce controlled muscle contractions, improve circulation, modulate neuromuscular activity, and reduce muscle tone. The combined application of SIS and mCIMT is expected to produce complementary effects by reducing spasticity physiologically while simultaneously promoting motor relearning and functional use of the hand.
This single-blinded randomized controlled trial will be conducted on 16 stroke patients recruited from a tertiary care hospital and allocated into two groups: mCIMT alone and SIS with mCIMT. The intervention will be administered over two weeks. Outcomes will be measured using the Modified Ashworth Scale, Fugl-Meyer Assessment for Upper Extremity, Nine Hole Peg Test, goniometry, and the DASH questionnaire.
The study intends to establish an effective, non invasive, multimodal rehabilitation approach for improving hand function, dexterity, and quality of life in stroke survivors.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 75.00 Year(s)(—)
- 性别
- All
入选标准
- •Participants of all genders from the age group of 18 to 75 years who are willing to participate.
- •With a score of more than grade 1 of Modified Ashworth scale.
- •3.With a score of more than grade 1 of Brunnstrom Stages Of Stroke Recovery.
- •4.Participants who shows at least 10° of active wrist extension, 10 degree of thumb abduction/extension, and 10 degree of extension in at least 2 additional digits on ipsilateral side.
排除标准
- •1.Other Neurological Conditions.
- •2.Other conditions affecting hand function like Burns, Rheumatoid Arthritis, Leprosy, Diabetic neuropathy.
- •3.Acute cardiac conditions.
- •4.Metallic implants, Cancer, Fever, Pregnancy.
研究者
Shreya Pande
KLE Institute of Physiotherapy
