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The Effectiveness of Telerehabilitation in Stroke Patients

G

Gazi University

Status

Completed

Conditions

Stroke

Treatments

Other: Exercise
Other: Home program

Study type

Interventional

Funder types

Other

Identifiers

NCT05128461
1-Stroke-CIMT-Telerehab.

Details and patient eligibility

About

Stroke, according to the definition of the World Health Organization (WHO); It is a syndrome characterized by a rapid settlement of signs and symptoms of focal loss of cerebral function without a cause other than vascular causes. As it is known, it is important for patients to regain functional skills in the upper extremities after stroke. Modified-Constraint Induced Movement Therapy (m-CIMT) is a versatile neurorehabilitation technique that aims to improve motor function in the hemiparetic upper extremity and increase its use in daily life activities. However, as in the Covid-19 pandemic, patients cannot always reach rehabilitation services. In such cases, telerehabilitation is a treatment option. There are a limited number of studies in which m-CIMT is applied according to the principle of telerehabilitation, which has become a necessity, especially due to the Covid-19 pandemic. Therefore, the aim of this study is to examine the effects of m-CIMT on upper extremity motor functions in stroke patients.

Full description

This study is a randomized controlled study. The patients will be randomly divided into two groups as exercise and control. Patients in both groups will be given lower-upper extremity exercises and gait training exercises selected according to the Bobath approach as a home program consisting of 10 exercises to be applied 5 days a week for 3 weeks. All patients will perform the same exercises. In addition, the exercise group will receive Modified-Constraint Induced Movement Therapy (m-CIMT) based telerehabilitation via video conferencing 5 days a week for 3 weeks. Patients in the m-CIMT group will be asked to restrict the movements of their less affected hands by using mitt for 5 hours a day/ 5 days a week for 3 weeks while the patients are awake. Evaluations for both groups will be made by a physiotherapist blinded to the study twice, at the beginning and 3 weeks later. As outcome measures functional performance, hand strength, activities of daily living and quality of life will be evaluated.

Enrollment

18 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-65 years of age
  • Being diagnosed with stroke for the first time by a doctor
  • Having been diagnosed with stroke at least 1 month ago
  • Mini-Mental Test Score more than or equal 24
  • In the upper extremities; Starting from the angle of full flexion, wrist extension of at least 20° or more, thumb extension or abduction of at least 10°, minimum extension of all other fingers at the metacarpophalangeal and interphalangeal joints
  • Having less than 2.5 points in the pre-treatment evaluation from both parts of MAG-28
  • Being able to stand for 2 minutes without any help by using the upper extremity as a support tool when necessary.
  • Absence of severe pain to affect the treatment
  • Absence of severe spasticity to affect the treatment (spasticity in any joint of the upper extremity ≤ 2 according to the Modified Ashworth Scale)

Exclusion criteria

  • Any orthopedic, vision, hearing or perception problems that may affect the research results
  • Having an additional neurological, cardiovascular, pulmonary or hormonal disorder that would prevent participation in the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

18 participants in 2 patient groups

Exercise Group
Experimental group
Description:
The group will receive modified-Constraint Induced Movement Therapy via telerehabilitation and a home exercise program.
Treatment:
Other: Exercise
Other: Home program
Control group
Active Comparator group
Description:
The group only will be given a home exercise program.
Treatment:
Other: Home program

Trial contacts and locations

1

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Central trial contact

Fettah SAYGILI, PT, M.Sc.

Data sourced from clinicaltrials.gov

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