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

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

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100004699
Enrollment
Unknown
Registered
2021-04-06
Start date
2021-04-06
Completion date
Unknown
Last updated
2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

dyskinesia caused by non-acute stage stroke

Interventions

Sponsors

Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

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 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

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.

Design outcomes

Primary

MeasureTime frame
general criterion;isokinetic muscle test outcome;Simplify Fugl-Meyer scoring;3-D gait analysis outcome;biochemical criterion;Modified Ashworth grading;MMT freehand muscle strength grading;Functional Independence Measure;

Countries

China

Contacts

Public ContactZhang Di
364557347@qq.com+86 13688420533

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026