Dual-Task Performance in Patients With Multiple Sclerosis
NCT03508284, Completed, Gazi University
Trial 8
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Dual-Task Performance in Patients With Multiple Sclerosis | ClinicalTrials.gov |
| NCT number | NCT03508284 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Enrollment | 60 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Gazi University | ClinicalTrials.gov |
| Conditions | Multiple Sclerosis | ClinicalTrials.gov |
| First posted | 2018-04-25 | ClinicalTrials.gov |
| Last updated | 2019-07-31 | ClinicalTrials.gov |
Registered outcomes 10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Timed Up and Go Test | ten minutes | Timed up and go test measures the time taken in seconds to arise from a standard chair, walk 3 m, turn through 180 degrees, walk back, and sit down again. Cognitive additional task (arithmetic): Individuals will be asked to perform tasks by counting backward from 3 to 3 from 100. Cognitive additional task (verbal): Individuals will be asked to fulfill their duties by producing a vegetable-fruit name. | ClinicalTrials.gov |
| Primary | Modified Sensory Organization Test | Fifteen minutes | The Modified Sensory Organization Test, which is performed using computerized posturography, measures postural sway in response to 4 different sensory conditions is measured using a force platform. * Cognitive additional task (arithmetic) * Cognitive additional task (verbal) | ClinicalTrials.gov |
| Primary | upper extremity function | ten minutes | 9-Hole Peg Test * Cognitive additional task (arithmetic) * Cognitive additional task (verbal) | ClinicalTrials.gov |
| Secondary | Sleep Quality: PSQI | 5-10 minutes | The Pittsburgh Sleep Quality Index (PSQI) assess sleep quality. It is completed in 5-10 minutes. It consists of seven subscales: subjective sleep efficiency, sleep latency, sleep duration, sleep quality, sleep disturbance, sleep medication use, and daytime dysfunction due to sleepiness. Subscales yield a score from 0 to 3 and PSQI total score of \>5 is indicative of poor sleep. | ClinicalTrials.gov |
| Secondary | Fatigue Severity | Five minutes | In the Fatigue Severity Scale (FSS), participants are asked to rate their fatigue level between 1 and 7 in the 9 statements (including motivation, exercise, physical functioning, carrying out duties, and interfering with work, family, or social life) during the last week. | ClinicalTrials.gov |
| Secondary | Balance Confidence | five minutes | Activities-specific Balance Confidence (ABC) is a scale in which the patient rates his perceived level of confidence while performing 16 daily living activities. | ClinicalTrials.gov |
| Secondary | Mood | one minute | Beck's Depression Inventory | ClinicalTrials.gov |
| Secondary | Visual attention and task switching | Five minutes | Trail Making Test | ClinicalTrials.gov |
| Secondary | selective attention | Five minutes | stroop test | ClinicalTrials.gov |
| Secondary | cognitive function | thirty minutes | The Brief Repeatable Battery of Neuropsychological Tests | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 16
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 2748771 | BACKGROUND | PubMed |
| 11548987 | BACKGROUND | PubMed |
| 11990874 | BACKGROUND | PubMed |
| 12617275 | BACKGROUND | PubMed |
| 12900694 | BACKGROUND | PubMed |
| 13688369 | BACKGROUND | PubMed |
| 14527120 | BACKGROUND | PubMed |
| 16277993 | BACKGROUND | PubMed |
| 17293726 | BACKGROUND | PubMed |
| 17337007 | BACKGROUND | PubMed |
| 19007738 | BACKGROUND | PubMed |
| 19026963 | BACKGROUND | PubMed |
| 20594850 | BACKGROUND | PubMed |
| 23200463 | BACKGROUND | PubMed |
| 24578463 | BACKGROUND | PubMed |
| 28138492 | BACKGROUND | PubMed |
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 4
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 |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)