Home-based rehabilitation for stroke patients with limb dysfunction
Effects of Appropriate Technology for Home-based Rehabilitation in Patients With Post-stroke Physical Dysfunction
NA · Harbin Medical University · NCT06437587
This study is testing if a home-based rehabilitation program can help stroke survivors with limb problems improve their movement and daily activities better than just regular care.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 72 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Harbin Medical University (other) |
| Locations | 1 site (Daqing, Heilongjiang) |
| Trial ID | NCT06437587 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of a home-based rehabilitation program using appropriate technology (S-HRAT) for stroke survivors experiencing limb dysfunction. The study involves 36 participants who will be randomly assigned to either a control group receiving usual care or an experimental group receiving usual care plus an 8-week S-HRAT training program. The primary focus is to assess improvements in motor function and activities of daily living, with additional evaluations on anxiety, depression, exercise adherence, and patient satisfaction. Assessments will take place at baseline, 8 weeks, and 12 weeks post-discharge.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have experienced a stroke and have limb dysfunction, within two weeks to six months post-onset.
Not a fit: Patients who are returning to a hospital or rehabilitation facility after discharge or have serious, life-threatening conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance motor function and daily living activities for stroke survivors at home.
How similar studies have performed: While this approach is innovative, similar studies have shown promise in enhancing rehabilitation outcomes for stroke patients through home-based interventions.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age≥18; * Patients diagnosed with cerebrovascular disease who have cerebral infarction or cerebral hemorrhage based on cranial CT or MRI and meet the diagnostic criteria; * Patients are in the non-acute phase, meaning between two weeks and six months after the onset of the disease; * Patients with limb dysfunction. Exclusion Criteria: * Return to a hospital or rehabilitation facility after discharge; * The patient has a history of mental illness and dyslexia; * Patients have a combination of serious, life-threatening conditions.
Where this trial is running
Daqing, Heilongjiang
- Daqing Oilfield General Hospital — Daqing, Heilongjiang, China (RECRUITING)
Study contacts
- Study coordinator: Xi Chen
- Email: chenxi3760@163.com
- Phone: 15945313760
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.
Conditions: Stroke, home-based rehabilitation, appropriate technology