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Clinical Trials in China / NCT06437587
Recruiting Not applicable

Effects of Appropriate Technology for Home-based Rehabilitation in Patients With Post-stroke Physical Dysfunction

NCT06437587 · tracked via the Priya Life Science China tracker
Sponsor
Xi Chen
Phase
Not applicable
Started
2024-06-01
Last updated
2024-09-23

Condition(s) studied

Stroke

Investigational drug(s) / intervention(s)

Home-based rehabilitation appropriate technology (S-HRAT) training

Home-based rehabilitation appropriate technology (S-HRAT) training: The S-HRAT training instruction consists of two phases: in-hospital training and post-discharge remote home training. Based on the S-HRAT list, we select individualized home rehabilitation training exercises for the participants and conduct five offline training instruction sessions one week before discharge to ensure that the participants master the correct method for each exercise and clarify precautions. At discharge, participants will receive an S-HRAT brochures, which will include detailed text, pictures and video demonstrations of exercises, to visualize the rehabilitation instructions and make them easy to understand. Participants learn how to use the S-HRAT booklet and follow a daily training program to complete the prescribed content. They will be asked to record a video of their training and send it to the researcher via WeChat for monitoring purposes and feedback.

Study summary

The goal of this clinical trial is to assess the effect of S-HRAT to improve patients' motor function and activities of daily living.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Daqing Oilfield General Hospital Daqing Heilongjiang Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06437587 on ClinicalTrials.gov ↗ ← All trials in China