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The Effectiveness of Telerehabilitation in Stroke Patients

The Effectiveness of Modified-Constraint Induced Movement Therapy Based Telerehabilitation in Stroke Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05128461
Enrollment
18
Registered
2021-11-22
Start date
2021-11-22
Completion date
2022-10-20
Last updated
2023-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

Stroke, Telerehabilitation, modified-Constraint Induced Movement Therapy, Upper Extremity

Brief summary

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.

Detailed 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.

Interventions

OTHERExercise

M-CIMT-based telerehabilitation will be implemented.

Lower and upper extremity exercises and gait training exercises selected according to the Bobath approach will be given as a home program consisting of 10 same exercises.

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

Two groups as exercise group and control group

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Voluntary movement and mobility-Post interventionAssessment will be conducted immediately after the intervention.Stroke Rehabilitation Assessment of Movement (STREAM)
Upper extremity motor ability-BaselineAssessment will be conducted before the intervention.Wolf Motor Function Test
Upper extremity motor ability-Post interventionAssessment will be conducted immediately after the intervention.Wolf Motor Function Test
Upper extremity motor function-BaselineAssessment will be conducted before the intervention.The Fugl-Meyer Assessment of the Upper Extremity
Upper extremity motor function-Post interventionAssessment will be conducted immediately after the intervention.The Fugl-Meyer Assessment of the Upper Extremity
Activities of daily living related to the upper extremity-BaselineAssessment will be conducted before the intervention.Motor Activity Log-28 (MAL-28) The minimum score that can be obtained from this scale is 0, and the maximum score is 5. Higher scores mean that the level of use and quality of use is better.
Activities of daily living related to the upper extremity-Post interventionAssessment will be conducted immediately after the intervention.Motor Activity Log-28 (MAL-28) The minimum score that can be obtained from this scale is 0, and the maximum score is 5. Higher scores mean that the level of use and quality of use is better.
Voluntary movement and mobility-BaselineAssessment will be conducted before the intervention.Stroke Rehabilitation Assessment of Movement (STREAM)

Secondary

MeasureTime frameDescription
Isometric hand strength-BaselineAssessment will be conducted before the intervention.J-Tech™
Isometric hand strength-Post interventionAssessment will be conducted immediately after the intervention.J-Tech™
Isometric pinch strength-BaselineAssessment will be conducted before the intervention.Baseline® pinch meter
Isometric pinch strength-Post interventionAssessment will be conducted immediately after the intervention.Baseline® pinch meter
manual dexterity performance-BaselineAssessment will be conducted before the intervention.nine-hole peg test (9-HTP)
manual dexterity performance-Post interventionAssessment will be conducted immediately after the intervention.nine-hole peg test (9-HTP)
level of independence in activities of daily living-BaselineAssessment will be conducted before the intervention.Functional Independence Measure
level of independence in activities of daily living-Post interventionAssessment will be conducted immediately after the intervention.Functional Independence Measure

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026