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HealthyNCT03733080

Large-Scale Online Studies of Early Motor Skill Learning

An observational study of Healthy, run by National Institute of Neurological Disorders and Stroke (NINDS) at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background: Our goal is to gain insight into early human motor skill learning by carrying out online substudies using online crowd-sourcing tools. Objective: To learn more about motor behavior in a large group of people using motor tasks, and questions. Eligibility: Adults ages 18 and older based in the U.S. Read more about this study

Who is it for?
Ages 18 to 120 years
Conditions the study is for
Healthy
How many people
2,529 participants
Where
1 siteUnited States
Study dates
9 Jan 2019to 17 Oct 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 18 to 120 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: A total of 2,529 volunteers have participated in this protocol. It is possible that some of these participants may have been NIH or NINDS employees, since participant identities were anonymous to the experimenters. Data aquired from 97 participants was used for testing and debugging the typing task application during initial technical development. These data are not useable for research purposes.

Who may be able to join

  • U.S.-based English speakers greater than 18 years of age are eligible to participate in the study.

Who cannot join

  • Subjects are excluded if they are less than 18 years of age. NIH and NINDS employees are not excluded from the study, since participation is anonymous and personal identifiers unknown to the experimenters.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • National Institute of Neurological Disorders and Stroke (NINDS)

    Bethesda, Maryland, 20892

Other trials in United States

About this study

Official title: Large-scale Online Studies of Motor Responses and Cognition

Background:

Our goal is to gain insight into early human motor skill learning by carrying out online substudies using online crowd-sourcing tools.

Read more

Objective:

To learn more about motor behavior in a large group of people using motor tasks, and questions.

Eligibility:

Adults ages 18 and older based in the U.S. who speak English

Design:

Participants will be recruited from a crowd-sourcing website like Amazon Mechanical Turk.

Participants will do online tasks. They can use their own computers anywhere with Internet access. They will not need to directly interact with researchers.

Participants will be asked for general data, like their age and gender. No personally identifiable data will be collected.

Participants will see a list of tasks on their computer screen. They will be able to choose tasks they wish to do. They will get a description of the experiment, how long it takes, and how much compensation they will get.

Participants will complete on their screen a motor behavioral task, a cognitive task, and/or a questionnaire. For example, they may be asked to press sequences of numbers on the keyboard or move the mouse when a stimulus appears on the screen. Experiments may last up to 1 hour.

Participants can complete as many experiments as they wish. They can quit at any point.

Read the detailed description

Objective:

Our overall goal in this protocol has been to gain insight into early motor skill learning (micro-learning) in large-scale healthy volunteer cohorts using online crowd-sourcing. We have used a simple keyboard typing task to study micro-offline performance improvements during early motor skill learning. This online approach limits the burden on participants (who perform tasks in the comfort of their homes instead of traveling to NIH) and substantially reduces burden on in-house human, financial and technical resources. Results from this protocol contribute to a better understanding of factors relevant to human motor skill learning, with important implications for the design of better motor learning and neurorehabilitative strategies after brain lesions. We had completed data collection for four aims under this protocol at the time we were informed by the NIH IRB that they determined this to be a thematic protocol (September 23, 2019).

The four specific aims addressed under this protocol are:

  1. Aim 1. To validate a motor skill learning task previously used by our group in lab-based studies {Bonstrup, 2019 #36} within an online, crowd-sourcing platform.
  2. Aim 2. To compare the influence of an interfering task applied during early ("early interference") vs late ("late interference") rest periods on motor learning, thus evaluating resistance to interference, a feature of consolidation.
  3. Aim 3. To evaluate the effects of a shorter practice period duration (i.e. - 5s vs. previously studied 10s duration) on micro-offline motor learning to gain insight into the impact of fatigue-related factors on learning.
  4. Aim 4. To evaluate the effects of randomly variable practice period durations between 5-10s in length on micro-offline gains

As instructed, the purpose of this amendment is to request authorization to proceed with data analysis and publication. No new experiments will be carried out under this protocol.

Study Population:

U.S.-based English speakers aged 18 and above were recruited under this minimal risk protocol. Participants completed an online task in the comfort of their own homes using the internet, and did not need to directly interact with the investigators. All participants were given an anonymized random ID by the on-line site. We did collect general demographic information including age (needed to determine elegibility), and gender, race and ethnicity (per IRB reporting requirements, i.e. - Cumulative Inclusion Enrollment Report). However, we did not collect personally identifiable information (PII) about the participants.

Design:

Under this protocol, we have conducted experiments supporting four aims using Amazon Mechanical Turk (AMT). All experiments consisted of a brief keyboard typing task where participants were asked to repeatedly type a 5-key sequence (4-1-3-2-4) as fast and as accurately as possible for several seconds (i.e. - practice trial). Each practice trial was followed by a rest period lasting several seconds. Following the task, participants completed a short questionnaire designed to query compliance with task instructions, and collect general demographic data required for IRB reporting. The average total time for participation across all experiments was approximately 20 minutes.

Outcome Measures:

The primary outcome measures for the keyboard typing task were correct sequence typing speed and typing accuracy. Microlearning scores were derived by quantifying the speed change between the end of a previous practice trial and the beginning of the subsequent one (micro-offline learning) and the speed difference between the beginning and end of the same practice trial (micro-online learning). Information from the questionaires related to task instruction compliance was primarily used to exclude data from further analysis if needed.

Conditions
Healthy
Keywords
AMT, Natural History

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT03733080
Study groupRoleWhat they receive
1ages 18 and older

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. data analysis

    Aim 1. To validate a motor skill learning task previously used by our group in lab-based studies {Bonstrup, 2019 #36} within an online, crowd-sourcing platform. Aim 2. To compare the influence of an interfering task applied during early ( early interference group) vs late ( late interference ) rest periods on stabilization of motor learning. Aim 3. To evaluate the effects of shorter practice period durations (i.e. - 5s vs. previously studied 10s duration) on micro-offline motor learning to gain insight into the impact of fatigue-relatedfactors on learning. Aim 4. To evaluate the effects of randomly variable practice period durations between 5-10s in length on micro-offline gains

    Measured: in data analysis

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Nov 2018
  2. Study start9 Jan 2019
  3. Primary completion17 Oct 2019
  4. Study completion17 Oct 2019

Resources

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
Case only
Time perspective
Cross-sectional
Enrolment
2,529 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03733080
Sponsor's protocol ID
999919012
Other IDs
19-N-N012
Status last verified
Apr 2025
First submitted
6 Nov 2018
Last updated
15 Apr 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Healthy, run by National Institute of Neurological Disorders and Stroke (NINDS) at 1 site in United States.

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 1 inclusion and 1 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 15 Apr 2025. 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 United States. 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?

data analysis (time frame: in data analysis). 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 15 Apr 2025.

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