Clinical Application of Portable Intelligent Multi Joint Isokinetic Training and Evaluation System Technology

Ran Shi90 enrolled

Overview

The goal of this clinical trial is to compare in describeparticipant population. The main question it aims to answer is:By using intelligent portable isokinetic tester and traditional isokinetic tester, isokinetic knee flexor and extensor muscles of stroke patients with hemiplegia were trained respectively, so as to observe and compare the effects of the two treatment methods. In addition, the therapeutic effect of the above two treatments was compared with that of exercise therapy alone. Participants will be divided into three groups: control group, intelligent isokinetic treatment group, and traditional isokinetic treatment group. Participants of both the control group and the two treatment groups received exercise therapy. On the basis of exercise therapy, participants of the intelligent isokinetic treatment group used the intelligent portable isokinetic tester to train the affected knee flexion and extensor muscle, while the participants of traditional isokinetic treatment group used the intelligent portable isokinetic tester to train the affected knee flexion and extensor muscle.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Stroke Hemiplegia Rehabilitation; Tobacco Use

Interventions

Intelligent portable isokinetic muscle strength test trainingDEVICE

The isokinetic training of knee flexors and extensors was carried out by using intelligent portable isokinetic muscle strength test training system

isokinetic muscle strength test trainingDEVICE

The isokinetic training of knee flexors and extensors was carried out by using isokinetic muscle strength test training system

without test trainingOTHER

Treatment was performed without using any isokinetic muscle strength test training system

Eligibility

Sex: ALLMin age: 25 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Clinical diagnosis of Cerebral apoplexy's Disease * Confirmed by CT or MR Examination of the head * First onset, duration ≤1 month * The lower extremity of the hemiplegic limb was above Brunnstrom stage III * Must be able to sign the informed consent form Exclusion Criteria: * Vital signs are unstable * Severe cognitive, visual and hearing impairment * Orthopaedic disease * Muscle pain lower extremity * Congenital disease * History of other encephalopathy * History of mental illness

Outcomes

Primary Outcomes

Body function

Evaluate lower limb motor function using the Fugl Meyer method (total lower limb motor score 0-34 points, total balance score 0-14 points).

Time frame: up to 1 month

Measured peak moment

Peak moment of knee joint at 60 °/s angular velocity in Nm

Time frame: up to 1 month

Secondary Outcomes

Satisfaction questionnaire survey

Survey of patients' comfort and satisfaction with the treatment process and effectiveness(score 0-100 points).

Time frame: up to 1 month

Clinical Application of Portable Intelligent Multi Joint Isokinetic Training and Evaluation System Technology

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts