CompletedNot Applicable

Upper Extremity Robotic Rehabilitation in Patients With Hemiplegia

Turkey (Türkiye)37 participantsStarted 2016-04-14

Plain-language summary

Comparison of Upper Extremity Robotic Rehabilitation Efficiency with Conventional Rehabilitation in Patients with Hemiplegia after Cerebrovascular Event

Who can participate

Age range

18 Years – 85 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Having a single stroke * Being an adult * Having a duration of 4 to 30 months after stroke * A score greater than 16 in mini-mental test * Upper extremity Brunnstrom stage 2 or higher * Being a fluent speaker in Turkish. Exclusion Criteria: * Severe apraxia * Skin ulcers * Multiple cerebrovascular events * Severe decompensated diseases (cardiopulmonary, neurological, orthopedic and psychiatric etc), cardiac pacemakers, severe neuropsychological impairment, * Neglect syndrome * Spasticity greater than 3 in Modified Ashworth Scale * Severe joint contractures * Botulinum toxin-A injection in their upper extremity and dose change in drugs for spasticity in the last 3 months.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Change from baseline hand grip strength at 4th week.

Timeframe: Up to 4 weeks

Change from baseline hand functions (Minnesota manuel dexterity test) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline hand functions (Purdue peg board) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline spasticity (Modified Ashworth Scale (MAS)) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline neurophysiological development (Brunnstrom stage) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline motor function (Fugl Meyer Assessment (FMA)) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline general function (Functional Independance Measure (FIM)) at 4th week.

Timeframe: Up to 4 weeks

Trial details

NCT IDNCT04393480

SponsorSahel Taravati, M.D.

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-04-14

View on ClinicalTrials.gov More Hemiplegia and/or Hemiparesis Following Stroke trials

Who can participate

Age range

18 Years – 85 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Change from baseline hand grip strength at 4th week.

Timeframe: Up to 4 weeks

Change from baseline hand functions (Minnesota manuel dexterity test) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline hand functions (Purdue peg board) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline spasticity (Modified Ashworth Scale (MAS)) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline neurophysiological development (Brunnstrom stage) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline motor function (Fugl Meyer Assessment (FMA)) at 4th week.

Timeframe: Up to 4 weeks

Change from baseline general function (Functional Independance Measure (FIM)) at 4th week.

Timeframe: Up to 4 weeks