Ignite Creation Date:
2024-05-06 @ 8:07 PM
Last Modification Date:
2024-10-26 @ 3:21 PM
Study NCT ID:
NCT06261099
Status:
RECRUITING
Last Update Posted:
2024-02-15
First Post:
2024-02-08
Brief Title:
Telerehabilitation-Based Early Upper Extremity Training in Stroke Patients
Sponsor:
Suleyman Demirel University
Organization:
Suleyman Demirel University
Study Overview
Official Title:
The Effect of Telerehabilitation-Based Early Upper Extremity Training on Upper Extremity Function and Proprioception in Stroke Patients
Status:
RECRUITING
Status Verified Date:
2024-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Telerehabilitation method which is an alternative to face-to-face rehabilitation practices for stroke patients who need intensive regular and long-term rehabilitation in the early period has been popularly used in recent years Telerehabilitation is a practice in which the patient participates in the treatment via digital media without the need for the patient to come to the clinic
Detailed Description:
After the sociodemographic data of the participants are recorded Mini Mental Test MMT will be applied to evaluate the cognitive status Upper extremity functions of patients eligible for the study will be evaluated with the Fugl-Meyer Upper Extremity Scale FM-UE proprioception evaluation will be evaluated with the Laser-pointer Assisted Angle Reproduction Test activities of daily living will be evaluated with the Modified Barthel Index and reaching performance will be evaluated with the Reaching Performance Scale Characteristics of the patients participating in the study and all outcome measurements before and after treatment will be evaluated by a blinded physiotherapist A researcher blinded to the exercise groups and evaluation results will perform the statistical analysis
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None