This protocol will investigate the effects of action observation therapy and robotic rehabilitation on upper extremity motor functions in subacute stroke patients. Firstly, for this purpose, conventional rehabilitation approaches will take 60 minutes before both treatment methods in stroke patients. The upper-limb conventional rehabilitation program will be applied to all patients according to their individual needs (60x3x8 minutes/day/week). This program will consist of purposeful clinical exercises with a physiotherapist. After the conventional rehabilitation, one of the groups will receive action observation therapy, while the other will receive robotic rehabilitation. Both additional treatment methods will also be applied for 60 minutes. Treatment durations of both additional treatments are the same (60x3x8 minutes/day/week). Assessments will be made three times (Beginning, 4th week, 8th week).
Randomization: The online randomization software (www.randomizer.org) will be used for the study. After randomization, patients will be divided into two groups (AOT group, Robotic group) Blinding: Due to the nature of the study, patient-practitioner blinding is not possible. But an independent expert will perform the statistical analysis, and single-blind will be provided. Estimating Sample Size: Gpower 3.1.9.7 software was used for sample size calculation. To calculate the effect size, the study of Lima and Christofoletti was taken as a reference, and the effect size was calculated as 1.29. The alpha error was accepted as 5% and the power of the study was 80%. Accordingly, considering that there may be missing data in the study, it was planned to include a minimum of 30 stroke patients. Statistical Analysis: Statistical Package for the Social Sciences (SPSS v11.5) program will be used for analysis. Whether the data is normally distributed or not will be questioned by the Shapiro-Wilks test and histogram curves. When the data are normally distributed, Independent Sample T-test will be used for comparisons between groups, and Paired-Sample T-test will be used for comparisons within groups. When the data do not show normal distribution, Mann-Whitney U Test will be used for intergroup comparisons and Wilcoxon Signed Rank Test will be used for in-group comparisons.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
30
Conventional treatment for the upper extremity will be applied according to the patient's individual needs. A physiotherapist will apply this method in the clinic for 60 minutes. The duration of treatment is 60x3x8 minutes/day/week. Other methods will be applied in addition to the conventional treatment program.
Robotic Rehabilitation
Action Observation Therapy (AOT)
Marmara University
Istanbul, Turkey (Türkiye)
Fugl Meyer Assessment for Upper Extremity
This form is used to detect healing in the upper extremity.
Time frame: Baseline
Fugl Meyer Assessment for Upper Extremity
This form is used to detect healing in the upper extremity.
Time frame: End of the 4th week
Fugl Meyer Assessment for Upper Extremity
This form is used to detect healing in the upper extremity.
Time frame: End of the 8th week
Wolf Motor Function Test
This test is used for the level of motor function.
Time frame: Baseline
Wolf Motor Function Test
This test is used for the level of motor function.
Time frame: End of the 4th week
Wolf Motor Function Test
This test is used for the level of motor function.
Time frame: End of the 8th week
Demographic Data Form
Informations about the patients
Time frame: Baseline
Functional Independence questionnaire
This form helps determine an individual's level of independence.
Time frame: Baseline
Functional Independence questionnaire
This form helps determine an individual's level of independence.
Time frame: End of the 4th week
Functional Independence questionnaire
This form helps determine an individual's level of independence.
Time frame: End of the 8th week
The Stroke-Specific Quality of Life Scale (SS-QoL)
This is a quality of life assessment scale specific to stroke patients. Individuals with a high quality of life also have a high score.
Time frame: Baseline
The Stroke-Specific Quality of Life Scale (SS-QoL)
This is a quality of life assessment scale specific to stroke patients. Individuals with a high quality of life also have a high score.
Time frame: End of the 4th week
The Stroke-Specific Quality of Life Scale (SS-QoL)
This is a quality of life assessment scale specific to stroke patients. Individuals with a high quality of life also have a high score.
Time frame: End of the 8th week
Box and Block Test
This test is used to evaluate gross motor function of the upper extremity.
Time frame: Baseline
Box and Block Test
This test is used to evaluate gross motor function of the upper extremity.
Time frame: End of the 4th week
Box and Block Test
This test is used to evaluate gross motor function of the upper extremity.
Time frame: End of the 8th week
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