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.
UNKNOWN
PHASE2/PHASE3
40 participants
INTERVENTIONAL
2012-10-31
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.
Compensatory Brain Activity in Older Adults.
NCT06235840
Computer-based Attention Training in Patients With Acquired Brain Injury
NCT02399293
Neural Bases of Cognitive Rehabilitation for Brain Injury
NCT01120756
Training Cognition With Neurofeedback After Stroke
NCT06852209
Computerized Cognitive Training for MCI
NCT03232047
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
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Working Memory Training
The subjects of experimental group received a series of working memory training, 30 min for 5 days per week during 6 weeks.
Working memory training
Non-Working Memory Training
The subjects of control group performed traditional cognitive rehabilitation without working memory training, 30 min for 5 days per week during 6 weeks.
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.
Working memory training
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Diagnosis of traumatic brain injury or stroke
* Course of disease within one year
* The score of MoCA test \> 24
* Able to understand instructions
Exclusion Criteria
* Hearing impairment or visual impairment
* History of taking psychiatric drugs
18 Years
55 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
China Rehabilitation Research Center
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yun XiaoPing
Director of Department of Rehabilitation Evaluation
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Xiaoping Yun, MD
Role: PRINCIPAL_INVESTIGATOR
Department of Rehabilitation Evaluation, China Rehabilitation Research Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Rehabilitation Evaluation, China Rehabilitation Research Center
Beijing, Beijing Municipality, China
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.
NSFC-81272165
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.