Perceptual Learning Study in Sensory and Motor Function
Trial Summary
What is the purpose of this trial?
The purpose of this study is to understand how the sensory and motor areas of the brain work together to keep a person's hand movements accurate (sensorimotor learning). The investigators hope this information may be useful one day to improve rehabilitation techniques in patients with brain lesions.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of this treatment in the Perceptual Learning Study in Sensory and Motor Function?
Research shows that sensory and motor learning can improve tactile and proprioceptive (sense of body position) abilities in stroke patients, suggesting that similar training might enhance sensory and motor functions in other contexts. Additionally, placebo effects, which are improvements due to belief in treatment rather than the treatment itself, can be conditioned and may contribute to perceived effectiveness.12345
Is perceptual learning in sensory and motor function safe for humans?
How does the Perceptual Learning Study in Sensory and Motor Function treatment differ from other treatments?
This treatment is unique because it combines perceptual learning with motor learning, which means it not only focuses on improving motor skills but also enhances sensory perception. This dual approach leads to changes in both sensory and motor areas of the brain, potentially offering more comprehensive improvements in sensorimotor function compared to treatments that target only motor or sensory systems separately.67111213
Research Team
Hannah Block
Principal Investigator
Indiana University, Bloomington
Eligibility Criteria
This trial is for right-handed individuals aged 18-45, free of COVID symptoms and fully vaccinated or with a recent negative test. Exclusions include BMI over 30, inability to perform tasks or follow instructions, IUD users without MR compatibility confirmation, claustrophobia, pregnancy, vision issues not correctable by MRI-compatible glasses at the center, neurological disorders or upper limb conditions.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Familiarization
Participants undergo a familiarization session for fMRI and the behavioral task
Main Session
Participants perform the main session tasks including resting state scans and behavioral tasks
Follow-up
Participants are monitored for any immediate effects post-session
Treatment Details
Interventions
- Control
- Motor learning
- Perceptual learning
Find a Clinic Near You
Who Is Running the Clinical Trial?
Indiana University
Lead Sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborator