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A clinical study on ankle proprioception and balance function in stroke patients

A clinical study on ankle proprioception and balance function in stroke patients

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054720
Enrollment
Unknown
Registered
2021-12-25
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Stroke

Interventions

conventional rehabilitation group:60 minutes of regular rehab and 20 minutes of power cycling
unilateral passive group:60 minutes of routine rehabilitation treatment and 20 minutes of passive ankle proprioception training on the affected side
Bilateral passive group:60 minutes of routine rehabilitation treatment and 20 minutes of bilateral passive ankle proprioception training.
Bilateral active-passive group:60 minutes of routine rehabilitation treatment and 20 minutes of bilateral passive ankle proprioceptive training after contralateral trigger.

Sponsors

Huashan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for stroke patients: (1) Voluntary participation, the patient himself understands and signs the informed consent form or his immediate family members sign the informed consent; (2) Meet the diagnostic criteria of the "Chinese Classification of Cerebrovascular Diseases 2015", and were diagnosed with cerebral infarction, cerebral embolism, cerebral hemorrhage, and unilateral limb motor dysfunction by cranial MRI or CT examination. (3) Initial onset, duration of 2 weeks to 6 months (subacute stage); (4) Men and women are not limited; aged 40 to 80 years; (5) The condition is stable, the consciousness is clear, the vital signs are stable, and the instructions can be understood and executed; (6) Blood pressure is controlled at <140/90mmHg; (7) Waterloo Predominant Foot Questionnaire (Revised): Right-handed; Edinburgh Predominant-handed Questionnaire: Right-handed; (8) Brunnstrom stage lower extremity above stage II; (9) Able to walk independently for more than 10 meters with assistive devices. 2. Inclusion criteria for non-stroke group: (1) Voluntary participation, I understand and sign the informed consent form or have their immediate family members sign the informed consent; (2) Men and women are not limited; aged 40 to 80 years; (3) No history of stroke; (4) Blood pressure is controlled at <140/90mmHg; (5) Waterloo Predominant Foot Questionnaire (Revised): Right-handed; Edinburgh Predominant-handed Questionnaire: Right-handed.

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for stroke patients: (1) Combined with other neuromusculoskeletal diseases, neurological diseases and vestibular system diseases that affect walking ability and balance function (such as: cerebellar injury, Parkinson's disease, peripheral neuropathy, Meniere's syndrome, various Patients with osteoarthritis, history of lower extremity surgery, history of ankle sprain within 10 years); (2) The modified Ashworth scale (MAS) score of the affected lower limb is greater than 2, and the joint has obvious contracture; (3) Patients with intracranial tumors, severe respiratory, heart, liver, kidney, endocrine and hematopoietic system diseases; (4) women who are pregnant; (5) Those who are participating in other clinical trials that affect the evaluation of the results of this study. 2. Exclusion criteria for non-stroke group: (1) Participating in other clinical trials that affect the evaluation of the results of this study; (2) There is a history of related diseases that will affect this study, such as: history of lower extremity surgery, history of ankle sprain within 10 years, etc.; (3) There are any circumstances that will cause this research to not be completed; (4) Women in pregnancy.

Design outcomes

Primary

MeasureTime frame
active movement extent discrimination assessment, AMEDA;"Rise-and-walk" timed test;10 meter walk test;

Secondary

MeasureTime frame
Berg balance scale;Single leg stance;Function in Sitting Test, FIST;

Countries

China

Contacts

Public ContactZhu Yulian

Huashan Hospital Affiliated to Fudan University

zhuyulian@fudan.edu.cn+86 138 1678 3039

Outcome results

None listed

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