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Randomized controlled clinical trials for rehabilitation efficacy of ''Triple Facilitation Therapy'' for stroke patients with dyskinesia at non-acute stage

Phase 1
Recruiting
Conditions
dyskinesia caused by non-acute stage stroke
Registration Number
ITMCTR2100004699
Lead Sponsor
Hospital of Chengdu University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Patients meet with following 8 criteria can be included in this study:
1.Meet with diagnostic criteria of stroke for the first time;
2.With lateral dyskinesia;
3.With MMT freehand muscle strength grading <5, and lowers limb muscle strength >2+;
4.With Modified Ashworth grading of muscle tension >0;
5.With course of disease >4 weeks;
6.With ages 20-80 years old, and who can cooperate with treatment actively;
7.Who can walk alone;
8.Who knows and agree with relevant research content and signs the informed consent form.

Exclusion Criteria

Patients meet with 1 of the following 8 criteria will be excluded in this study:
1. Dyskinesia caused by other diseases and causes, such as Parkinson's disease, Parkinson's syndrome, progressive supranuclear palsy, hepatolenticular degeneration, essential tremor, multiple system atrophy, chorea, throwing syndrome, myoclonus, dystonia, tourette syndrome, and so on;
2. With serious diseases, such as uncontrollable hypertension, arrhythmia, serious coronary heart disease, diabetes complications are not well controlled, or have epilepsy, serious organ failure and second attack of stroke, and so on;
3. With unstable vital signs;
4. Who is susceptible to co-infection, bleeding, tumor, pregnant women, postoperative dysfunction patients;
5. Who receives other traditional Chinese medicine rehabilitation intervention except acupuncture and pestle during treatment;
6. With language or cognitive impairment, therefore can not understand the instructions to communicate or cooperate;
7. With previous mental illness history or long-term use of sedatives;
8. With other diseases to exercise.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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