Effect of Robotic Therapy on Upper Extremity With Stroke

NCT ID: NCT05815823

Last Updated: 2023-04-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-01-01

Study Completion Date

2017-01-01

Brief Summary

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The purpose of this study is to determine how adding virtual reality assisted robotic treatment to traditional rehabilitation affects stroke patients' pain levels, functional status, and daily living activities.After conventional and robotic therapy Each patient was evaluated The Barthel Index (BI), the Fugl Meyer Assessment Upper Extremity (FMA-UE), and the Visual Analogue Scale (VAS) were used to assess the patients' pain, daily living activities, and upper extremity motor function.

Detailed Description

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The purpose of this study is to determine how adding virtual reality assisted robotic treatment to traditional rehabilitation affects stroke patients' pain levels, functional status, and daily living activities.

Materials and Methods: The study included 40 stroke patients. Two groups of patients were created. Group I also underwent 20 sessions of upper extremity robot-assisted therapy for 4 weeks, 5 days a week, for 30 minutes per session, in addition to receiving conventional therapy (5 days a week for 4 weeks, 1 hour each day). Group II only got traditional therapy. Each patient was assessed both before and after the procedure.

The Barthel Index (BI), the Fugl Meyer Assessment Upper Extremity (FMA-UE), and the Visual Analogue Scale (VAS) were used to assess the patients' pain, daily living activities, and upper extremity motor function.

Conditions

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the Effect of Virtual Reality on Stroke Rehabilitation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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conventional therapy

20 sessions of conventional therapy was applied for 5 days a week for 4 weeks, 1 hour a day

Group Type EXPERIMENTAL

conventional therapy

Intervention Type OTHER

streching, range of motion, strengthening, balance and walking exercise

robot-assisted therapy

20 sessions of upper extremity robot-assisted therapy was applied for 4 weeks, 5 days a week, 30 minutes a day.

Group Type EXPERIMENTAL

robotic exercise therapy

Intervention Type OTHER

Functional exercise programs such as collecting rain in a glass, grating vegetables, goalkeeper, cleaning the stove, watering flowers, wiping windows, catching fish, and exploring landscapes were applied by robotic games to the patients

conventional therapy

Intervention Type OTHER

streching, range of motion, strengthening, balance and walking exercise

Interventions

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robotic exercise therapy

Functional exercise programs such as collecting rain in a glass, grating vegetables, goalkeeper, cleaning the stove, watering flowers, wiping windows, catching fish, and exploring landscapes were applied by robotic games to the patients

Intervention Type OTHER

conventional therapy

streching, range of motion, strengthening, balance and walking exercise

Intervention Type OTHER

Other Intervention Names

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robotic exercise

Eligibility Criteria

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Inclusion Criteria

\- Ischemic or hemorhagic hemiplegia

* Brunnstrom upper extremity motor stage ≥3
* At least 3 months have passed
* Modified Ashworth Score ≤2
* 18-85 year old patients with diagnosis of stroke

Exclusion Criteria

* Aphasia
* Cognitive impairment
* mini mental test \<24
* deformity and / or contracture in the upper extremity
* Patients diagnosed with KBAS
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul Physical Medicine Rehabilitation Training and Research Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Canan Avcı

Specialist of physical medicine and rehabilitation

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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2015/14/01

Identifier Type: -

Identifier Source: org_study_id

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