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NCT Number: NCT03979235

Developing Effectiveness Evaluation and Therapeutic Programs of Rehabilitation

Using robotics, sensors, and sEMG to develop clinic-oriented quantitative effectiveness evaluation and individualized programs of rehabilitation

Recruiting

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Key information

Conditions

Healthy Volunteers Deglutition Disorders Digestive System Diseases Dysphagia Esophageal Diseases Gastrointestinal Diseases Motor Deficits Nervous System Diseases Neurologic Manifestations Otorhinolaryngologic Diseases Pathological Conditions, Signs and Symptoms Pharyngeal Diseases Signs and Symptoms

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

National Research Center for Rehabilitation Technical Aids

Beijing, 100176, China

Location status: Recruiting

Location contact

PX Wei, Dr.

CONTACT

[email protected]

86-10-58122921

About this study

Using robotics, sensors, sEMG or other methods to develop clinic-oriented quantitative effectiveness evaluation and individualized programs of rehabilitation

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(for healthy people):

  • no history of psychological/psychotic problems, no history of important diseases.

Exclusion criteria

(for healthy people):

  • history of psychological/psychotic problems

Inclusion criteria

(for patients with motor deficits or dysphagia):

  • patients with motor function impairment such as post stroke hemiplegia.

Exclusion criteria

(for patients with motor deficits or dysphagia):

  • cognitively or physically unable to cooperate with the examiner to finish the test

Treatment and study plan

Motor function assessment

Diagnostic Test

perform motor function assessment by using scales, sEMG, and inertia sensors

Primary outcomes

  1. Motor function assessment

    Time frame: Change from Baseline scores at 1 month

    Fugl-Meyer Assessment

Secondary outcomes

  1. surface EMG

    Time frame: Change from Baseline status at 1 month

    high-density surface EMG

  2. Kinematics test

    Time frame: Change from Baseline status at 1 month

    Using inertia sensors to assess kinematics during movement

Study contacts

Contact information is provided by the study sponsor or research team.

LT Wang, PhD

CONTACT

[email protected]

86-10-58122882

PX Wei, PhD

CONTACT

[email protected]

86-10-58122921

Sponsors and collaborators

Lead sponsor

National Research Center for Rehabilitation Technical Aids

Other

Registry information

Official study title

Developing Clinic-oriented Quantitative Effectiveness Evaluation and Individualized Therapeutic Programs of Rehabilitation

Important dates

Study start
2019
Primary completion
2026
Study completion
2026
First posted
Jun 7, 2019
Registry last updated
May 23, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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