Trial · NCT03817086
Physical and Mental Practice for Bimanual Coordination Rehabilitation
NCT03817086, Not applicable, Completed, Kessler Foundation
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Physical and Mental Practice for Bimanual Coordination Rehabilitation. Trials, record NCT03817086. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03817086
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Physical and Mental Practice for Bimanual Coordination Rehabilitation
- NCT number
- NCT03817086
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 19 participants, actual
- Lead sponsor
- Kessler Foundation
- Conditions
- Traumatic Brain Injury, Weakness, Muscle, Coordination Impairment
- Interventions
- Hand coordination and mental practice, Hand coordination and action observation
- First posted
- 2019-01-25
- Last updated
- 2022-10-14
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Maximum voluntary contraction | Pretest (before training), Posttest (immediately after end of training), Retention test (3 weeks after end of training) | maximum force exerted by each hand during squeezing a handgrip force sensor |
| Primary | Change in Reaction Time | day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 8, day 9, day 10, day 11, day 12 | Reaction time is the time between real movement, and the time participant was instructed to move. This reaction time will be recorded for every training trial. The average of reaction time in each training day (total 12) will be used to examine the change in performance (slope) across the 12 training days, from day 1 until day 12 of the intervention. |
| Primary | Change in Percent of Error in force matching | day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 8, day 9, day 10, day 11, day 12 | Percent of error is the mismatch between the force exerted by the participant and the required force as per the instructions in each training trial. This Percent of Error will be recorded for every training trial. The average of errors in each training day (total 12) will be used to examine the change (slope) in performance across the 12 sessions (days) of the intervention. |
| Primary | Change in wolf motor function test | Pretest (before training), Posttest (immediately after end of training), Retention test (4 weeks after end of training) | assessment of upper extremity function |
| Primary | Change in within-brain effective connectivity | Pretest (before training), Posttest (immediately after end of training) | connectivity between sensorimotor and attention network during inphase and out-phase hand coordination task |
| Primary | Change in resting state function connectivity | Pretest (before training), Posttest (immediately after end of training) | connectivity between sensorimotor and attention network at rest |
| Primary | Change in brain structural connectivity (DTI) | Pretest (before training), Posttest (immediately after end of training) | cerebrospinal tract connectivity |
| Secondary | stroop effect test | Pretest (before training), Posttest (immediately after end of training), Retention test (3 weeks after end of training) | neuropsychology assessments of reaction time |
| Secondary | trail making test | Pretest (before training), Posttest (immediately after end of training), Retention test (3 weeks after end of training) | neuropsychology assessments of task switching and visual attention |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests4
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
| Task Switching Test | Secondary outcome | ConductCognition |
| Trail Making Test A | Secondary outcome | ConductCognition |
| Trail Making Test B | Secondary outcome | ConductCognition |
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03817086
GET https://conductscience.org/api/trials/v1/NCT03817086/registered