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Mind over bionic hand: can imagining movements improve prosthetic control?

NCT ID NCT06541379

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 15, 2026 · Updated 2 times

Summary

This study looks at how well people with below-elbow amputations can imagine movements (motor imagery) and whether that skill helps them use their myoelectric prosthetic arm more effectively. Researchers will compare 30 amputees with a control group, using questionnaires and mental rotation tests. The goal is to understand the link between mental imagery, arm function, and body awareness, which could lead to better rehabilitation strategies.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this research could help design better rehabilitation programs that improve how well people use their myoelectric prostheses.
What could go wrong
This is a small observational study with only 30 participants, so results may not apply to everyone. It measures abilities and perceptions, not a treatment, so direct benefits are limited.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

30 people

The number who actually took part.

Started

Jun 2025

Finished

Jun 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Being an amputee using a unilateral transradial and myoelectric prosthesis and control group

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Amputee group inclusion criteria * Being an amputee using a unilateral transradial and myoelectric prosthesis * Having at least 6 months of prosthesis experience * Having a maximum score of 15 on the Beck Depression Inventory * Having a minimum score of 26 on the Standardized Mini Mental Test * Being willing to participate in the study Control Group inclusion criteria * Being between the ages of 18-65 * Having a minimum score of 26 on the Standardized Mini Mental Test * Having signed the Informed Voluntary Consent Form * Having a maximum score of 15 on the Beck Depression Inventory * Being literate Exclusion Criteria: Amputee group exclusion criteria * Having another physical problem other than amputation * Having a diagnosed cognitive disorder * Not being able to read or write Exclusion criteria for the control group from the study * Having any neurological, orthopedic, psychological (such as schizophrenia, psychosis) and systemic problems * Having an unchangeable visual or auditory disability

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Istanbul Medipol University

    Istanbul, Beykoz, 34158, Turkey (Türkiye)

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