Normal VolunteersNCT02828813
Neural Mechanisms of Motor and Cognitive Networks
An observational study of Normal Volunteers and Cognition Disorders, run by National Research Center for Rehabilitation Technical Aids at 1 site in China.
Trial summary
This study investigates the neural mechanisms of motor and cognitive networks using cognitive assessment, reaction time measurement, high-density EEG and fMRI. Read more about this study
- Who is it for?
- Ages 14 to 80 yearsHealthy volunteers can take part
- Conditions the study is for
- Normal Volunteers, Cognition Disorders, Motor Disorders
- How many people
- 120 participants
- Where
- 1 siteChina
- Study dates
- Jun 2016to Feb 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 14 to 80 years
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Healthy Volunteers: Advertising recruitment Persons with cognitive impairments: from inpatients and outpatients Persons with motor deficits: from inpatients and outpatients
Who may be able to join
- right handed,
- no history of psychological/psychotic problems,
- no history of important diseases.
- right handed
- in a stable condition
- ability to follow complex commands
Who cannot join
- Being Pregnant or breast feeding
- having any non-MRI compatible conditions
- having any non-MRI compatible conditions
- inability to perform required tasks
Trial locations and contacts
1 site in 1 country.
China1 site
National Research Center for Rehabilitation Technical Aids
Beijing, 100176
About this study
This study investigates the neural mechanisms of motor and cognitive networks using cognitive assessment, reaction time measurement, high-density EEG and fMRI.
- Conditions
- Normal Volunteers, Cognition Disorders, Motor Disorders
- Medical subject headings
- Cognition Disorders, Motor Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Normal | healthy subjects | |
| CogImpair | persons with cognitive impairments | |
| MotorDeficits | persons with motor deficits |
What is being measured
The primary outcome is the main question the study is designed to answer.
cognitive assessment scores
Measured: within one week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jul 2016 (estimated)
- Study startJun 2016
- Primary completionFeb 2019
- Study completionFeb 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Normal VolunteersStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Ecologic or community
- Time perspective
- Cross-sectional
- Enrolment
- 120 participants (actual)
Sponsor and investigators
- Lead sponsor
- National Research Center for Rehabilitation Technical Aids
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Pengxu Wei, National Research Center for Rehabilitation Technical Aids
- Investigators
- PX Wei, Dr., Principal investigator, National Research Center for Rehabilitation Technical Aids
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02828813
- Sponsor's protocol ID
- NRRA201607
- Status last verified
- Mar 2019
- First submitted
- 5 Jul 2016
- Last updated
- 13 Mar 2019
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No: no plan to share data
Study at a glance
From the registry record, last updated by the sponsor on 13 Mar 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Neural Mechanisms of Motor and Cognitive Networks
- ClinicalTrials.gov ID
- NCT02828813
- Acronym / sponsor ID
- NRRA201607
- Conditions
- Normal Volunteers, Cognition Disorders, Motor Disorders
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 120 participants (actual)
- Lead sponsor
- National Research Center for Rehabilitation Technical AidsUniversity, hospital or other
- Study start
- Jun 2016
- Primary completion
- Feb 2019 (actual)
- Study completion
- Feb 2019 (actual)
- First posted
- 12 Jul 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study investigates the neural mechanisms of motor and cognitive networks using cognitive assessment, reaction time measurement, high-density EEG and fMRI.
Study design
- Observational model
- Ecologic or community
- Time perspective
- Cross-sectional
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Normal | – | –healthy subjects |
| CogImpair | – | –persons with cognitive impairments |
| MotorDeficits | – | –persons with motor deficits |
Who may qualify
- Ages
- 14 to 80 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Healthy Volunteers: Advertising recruitment Persons with cognitive impairments: from inpatients and outpatients Persons with motor deficits: from inpatients and outpatients
Key inclusion criteria (6 listed)
- right handed,
- no history of psychological/psychotic problems,
- no history of important diseases.
- right handed
- in a stable condition
Key exclusion criteria (4 listed)
- Being Pregnant or breast feeding
- having any non-MRI compatible conditions
- having any non-MRI compatible conditions
- inability to perform required tasks
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
cognitive assessment scores
Time frame: within one week
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Mar 2019.
- Individual participant dataSharing planned: No. no plan to share data
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
PX Wei, Dr. principal investigator
National Research Center for Rehabilitation Technical Aids
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Normal Volunteers and Cognition Disorders, run by National Research Center for Rehabilitation Technical Aids at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 13 Mar 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
cognitive assessment scores (time frame: within one week). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Mar 2019.