Comparing intelligent and traditional muscle training for stroke rehabilitation
Clinical Application of Portable Intelligent Multi Joint Isokinetic Training and Evaluation System Technology
This study is testing whether a new smart training system can help stroke patients regain muscle strength better than traditional training methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 25 Years to 65 Years |
| Sex | All |
| Sponsor | Qianfoshan Hospital Academic / other |
| Locations | 1 site (Jinan, Shandong) |
| Trial ID | NCT06153992 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of a portable intelligent isokinetic training system compared to a traditional isokinetic training system for stroke patients with hemiplegia. Participants will be divided into three groups: a control group receiving standard exercise therapy, an intelligent isokinetic treatment group, and a traditional isokinetic treatment group. The study will assess the impact of these training methods on knee flexor and extensor muscle strength. The goal is to determine which approach yields better rehabilitation outcomes for patients.
Who should consider this trial
Good fit: Ideal candidates are stroke patients with hemiplegia who are within one month of their first onset and have a lower extremity muscle function above Brunnstrom stage III.
Not a fit: Patients with unstable vital signs, severe cognitive impairments, or other significant health issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance rehabilitation strategies for stroke patients, leading to improved muscle strength and recovery.
How similar studies have performed: While similar approaches have been explored, this specific use of a portable intelligent isokinetic system in stroke rehabilitation is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Jinan, Shandong
- Intelligent Multi Joint Isokinetic — Jinan, Shandong, China (Recruiting)
Study contacts
- Study coordinator: Ran Shi, doctor
- Email: zm17686689905@126.com
- Phone: 17686689905
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.