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OpenTrials
Completed

NCT Number: NCT07425158

Differences in Treatment Characteristics and Patient and Therapist Satisfaction Between Robot Assisted Therapy and Conventional Occupational Therapy Among Individuals Post Stroke

The purpose of this study is to compare the differences in treatment characteristics and patient and therapist satisfaction, between Robot Assisted Therapy (RAT) and Conventional Occupational Therapy (COT) single session in individuals post stroke.

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Key information

About this study

Method and research procedure: The study will include 30 sub-acute post stroke patients, aged 18-85, with severe motor impairment in the upper limb and with normal-mild cognitive ability, hospitalized at the Loewenstein Rehabilitation Hospital. Each subject will receive two 30-min treatment sessions, one Conventional Occupational Therapy (COT) and one Robot Assisted Therapy (RAT). Before and during each session, the Visual Analogue Scale (VAS) for reporting the level of pain will be administered. The number of repetitions and compensations will be counted by observation. After each session, a subjective satisfaction questionnaire regarding the treatment will be administered.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 to 85 year old following stroke (first-ever stroke).
  • Individuals in the sub-acute phase (up to three months)
  • Intact cognitive function (score > 21 points on the Mini Mental State Examination)
  • Sever weakness of the affected upper limb (score 5-20 points on the FMA)
  • Understanding and reading Hebrew
  • Normal or corrected eyesight.
  • Subjects were at least in one session of RAT and one session of COT

Exclusion criteria

  • Neurological, cardio-vascular or orthopedic impairment, unrelated to the stroke, which restrict upper limb function.
  • High muscle tone (score > 4 in Modified Ashworth Scale)
  • Apraxia (score <68 in De Renzi Apraxia Test)
  • Severe Sensory impairment.

Treatment and study plan

Robot Assisted Therapy (RAT)

Other

Robot Assisted Therapy (RAT): 30-min treatment session of active- assisted movements of shoulder and elbow, using a robotic arm and a computer screen, provides different exercises according to the motor ability of the patient. The robot provides proximal upper limb training in a three-dimensional (3D) environment. The occupational therapist will be planning the treatment by determining the range of motion, the amount of help and support and the level of difficulty of the game.

Conventional occupational therapy (COT): 30-min treatment session of active- assisted movements of the shoulder and elbow, using conventional facilities and devices. Treatment includes passive range of motion exercises and active- assistive exercises. The level of support and help will be determined by the occupational therapist.

Other names: Conventional occupational therapy (COT)

Primary outcomes

  1. Observation

    Time frame: 30 min

    The number of repetitions and compensations will be counted by observation

Secondary outcomes

  1. VAS

    Time frame: 1min

    The Visual Analogue Scale (VAS) is a common scale for estimating pain level from one to ten.

  2. Questionnaire

    Time frame: 5 min

    A subjective satisfaction questionnaire regarding the treatment will be administered.

Sponsors and collaborators

Lead sponsor

linor kennet

Other

Collaborators

  • Tel Aviv University

Registry information

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Feb 20, 2026
Registry last updated
Feb 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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