Effects of Neurofeedback and Transcranial Pulse Stimulation on Attention
NCT ID: NCT05834920
Last Updated: 2025-03-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
180 participants
INTERVENTIONAL
2023-03-17
2025-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Does Transcranial Magnetic Stimulation of the Cingulate Cortex Modulate the Perception of Dyspnoea?
NCT00830921
The Effect of TPS on Cognitive Functions in Older Adults With MCI
NCT06407141
The Effectiveness of rTMS on Improving Food Craving and Weight Control in Adults Without Serious Mental Illness
NCT07106398
Non Invasive Brain Stimulation Effects on Attentional Performance in ADHD Adults
NCT02286349
Transcranial Pulse Stimulation on Motor Cortex
NCT06312930
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Neurofeedback
Neurofeedback
Participants will engage in a neurofeedback game designed to increase the ratio of theta/beta frequency bands in electroencephalography measurement. This intervention will be delivered for up to 12 sessions within 4 weeks.
Transcranial pulse stimulation
Transcranial pulse stimulation (TPS)
Participants will be treated with the TPS device NEUROLITH (Storz Medical AG). Treatments will be administered for up to 12 sessions within 4 weeks, each session consisting of 6000 TPS pulses of 0.2 mJ/mm².
Waitlist
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Transcranial pulse stimulation (TPS)
Participants will be treated with the TPS device NEUROLITH (Storz Medical AG). Treatments will be administered for up to 12 sessions within 4 weeks, each session consisting of 6000 TPS pulses of 0.2 mJ/mm².
Neurofeedback
Participants will engage in a neurofeedback game designed to increase the ratio of theta/beta frequency bands in electroencephalography measurement. This intervention will be delivered for up to 12 sessions within 4 weeks.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Right-handed
* Normal/corrected hearing and vision
* Having basic literacy skills
* Having sustained attention scores below the threshold
Exclusion Criteria
* Having mild cognitive impairment
* Showing symptoms of depression and anxiety
* Having intellectual disability based on IQ scores
* Having diagnoses of any psychiatric or cognitive disorders besides attention deficit hyperactivity disorder (ADHD) inattentive and combined types
* Having long-term history of smoking cigarettes
* Engaged in alcohol and/or substance abuse
* Having history of hemophilia or other blood clotting disorders or thrombosis
* Having corticosteroid treatment within the last six weeks before first intervention
* Having contraindications for MRI scanning
20 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
The University of Hong Kong
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Maria Teresa Wijaya
Post-doctoral Fellow
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
HKU InnoCentre of Clinical Neuropsychology
Hong Kong, , Hong Kong
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
HKUNFBTPS
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.