The Effects of Telerehabilitation in Chronic Hemiplegic Patients

Sponsor
Hasan Kalyoncu University (Other)
Overall Status
Completed
CT.gov ID
NCT05897762
Collaborator
(none)
40
1
1
12
3.3

Study Details

Study Description

Brief Summary

The present study was conducted to investigate the effects of telerehabilitation on upper extremity functions and activities of daily living in chronic hemiplegic patients.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Tele rehabilitation Group
N/A

Detailed Description

A total of 40 chronic hemiplegic subjects were included in the study. The patients were divided into 2 groups by simple randomization method. As the Telerehabilitation Group (TR), Group 1 completed the treatment program, which included upper extremity and lower extremity strengthening exercises, for eight weeks, three days a week for 45-60 minutes, 10 repetitions, with online supervision. Group 2 was planned as a face-to-face training group and the same exercises were performed in the clinical setting, accompanied by a physiotherapist. The evaluations were made before and after the treatment. The Modified Ashworth Scale was used for upper extremity spasticity evaluation. The Wolf Motor Function Test was used to evaluate upper extremity functionality. The Barthel ADL Index was used to evaluate Activities of Daily Living (ADL). The Brunnstrom Staging Survey was used to evaluate the level of motor recovery. The Treatment Satisfaction Inquiry Survey was used to evaluate the satisfaction of the patients with the treatment method. Heart Rate (HR) values and oxygen saturation (SaO2) were measured with Pulse Oximetry to monitor vital signs.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
The Effects of Telerehabilitation on Upper Extremity Functions and Activities of Daily Living in Chronic Hemiplegic Patients
Actual Study Start Date :
Jan 1, 2021
Actual Primary Completion Date :
Jun 1, 2021
Actual Study Completion Date :
Jan 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Clinic Grup

the same exercises were performed in the clinical setting, accompanied by a physiotherapist. The evaluations were made before and after the treatment.

Behavioral: Tele rehabilitation Group
It has been determined that the telerehabilitation method applied in chronic hemiplegic patients increases daily living activities, upper extremity functionality, and spasticity levels decrease.

Outcome Measures

Primary Outcome Measures

  1. spasticity levels [Pre-Treatment and post treatment evaluations will ve recorded. (8 Weeks periods)]

    Spasticty will ve evaluated with Modifiye Ashworth Scale

  2. Upper Extremity functionality [Pre-Treatment and post treatment evaluations will ve recorded. (8 Weeks periods)]

    Upper extremity functionality evaluated with DASH

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Having been diagnosed with stroke between the ages of 40-70

  • It has been 12 months since the stroke

  • Individuals with upper extremity spasticity level (Modified Ashworth Scale (MAS) score ≤ 3)

  • Hand and upper extremity values above 3 according to Brunnstrom motor staging

  • Individuals with ischemic, middle cerebral artery involvement will be taken.

Exclusion Criteria:
  • Having advanced apraxia and aphasia

  • Patients who do not have the cooperation to perform verbal commands and exercise training

  • Patients who have undergone any botulinum toxin application in the last 6 months

  • Patients with significant visual and hearing loss

  • Individuals who do not have the necessary technological competence to provide remote video communication at home will not be accepted.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hasan Kalyoncu University Gaziantep Turkey 27010

Sponsors and Collaborators

  • Hasan Kalyoncu University

Investigators

  • Study Director: Deniz Kocamaz, Assist Prof, Hasan Kalyoncu University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hacer Karakurt, Student, Hasan Kalyoncu University
ClinicalTrials.gov Identifier:
NCT05897762
Other Study ID Numbers:
  • HasanKU"
First Posted:
Jun 9, 2023
Last Update Posted:
Jun 9, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hacer Karakurt, Student, Hasan Kalyoncu University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 9, 2023