Trial · NCT03478059
Dual-task Assessment and Rehabilitation for Individuals With Residual Symptoms After mTBI
NCT03478059, Not applicable, Completed, Allina Health System
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Dual-task Assessment and Rehabilitation for Individuals With Residual Symptoms After mTBI. Trials, record NCT03478059. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03478059
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Dual-task Assessment and Rehabilitation for Individuals With Residual Symptoms After mTBI
- NCT number
- NCT03478059
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 24 participants, actual
- Lead sponsor
- Allina Health System
- Conditions
- Brain Injury Traumatic Mild, Concussion, Brain
- Interventions
- Cognitive and Motor Dual-task Intervention
- First posted
- 2018-03-27
- Last updated
- 2019-08-30
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in peak velocity turns during Instrumented Stand and Walk Test | At baseline and after 6 weeks of intervention | Change in peak velocity during 180 degree turns during Instrumented Stand and Walk Test in single task (ST) and dual-task (DT) conditions. DT condition involves grid memorization task. |
| Secondary | Change in peak turning velocity during walking a custom turning course | At baseline and after 6 weeks of intervention | Change in peak turning velocity during walking a custom turning course in ST and DT conditions. |
| Secondary | Change in peak turning velocity during running an agility course | At baseline and after 6 weeks of intervention | Change in peak turning velocity during running an agility course in ST and DT conditions. |
| Secondary | Change in medial -lateral (coronal plane) sway area during eyes closed, narrowed stance | At baseline and after 6 weeks of intervention | Change in medial -lateral (coronal plane) sway area during eyes closed, narrowed stance in ST and DT conditions. |
| Secondary | Change in Beck Depression Inventory-II | At baseline and after 6 weeks of intervention | Change in Beck Depression Inventory-II: 21 item self-administered questionnaire that measures intensity of depression. |
| Secondary | Change in Beck Anxiety Inventory | At baseline and after 6 weeks of intervention | Change in Beck Anxiety Inventory: 21 item self-administered questionnaire measuring subjective, somatic, or panic-related symptoms of anxiety. |
| Secondary | Change in Patient-specific Functional Scale | At baseline and after 6 weeks of intervention | Change in Patient-specific Functional Scale -quantifies the amount of functional limitation secondary to symptoms in up to 3 activities that are relevant to the individual patient. 0 to 10 scale, where 0 = unable to perform activity and 10 = able to perform activity at same level as before injury or problem. |
| Secondary | Change in Neurobehavioral Symptom Inventory (NSI) | At baseline and after 6 weeks of intervention | Change in Neurobehavioral Symptom Inventory (NSI): Self-report of residual symptoms "in last 2 weeks", a measure of post-TBI symptom severity, 0-4 scale on 22 symptom questions. |
| Secondary | Rey Auditory Verbal Learning Test Score | At baseline | Rey Auditory Verbal Learning Test which measures verbal learning and memory (short-term) |
| Secondary | Comprehensive Trails Making Test Score | Baseline | Comprehensive Trails Making Test which measures set shifting, attention, psychomotor speed |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
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.
Tests3
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 |
| Verbal Fluency | Secondary outcome | ConductCognition |
| Verbal Learning | 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/NCT03478059
GET https://conductscience.org/api/trials/v1/NCT03478059/registered