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Trial · NCT03847545

Muscle Strain in Multiple Sclerosis Patients Measured by Ultrasound Speckle Tracking Technique

NCT03847545, Not applicable, Completed, University of Southern Denmark

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Muscle Strain in Multiple Sclerosis Patients Measured by Ultrasound Speckle Tracking Technique. Trials, record NCT03847545. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03847545

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Muscle Strain in Multiple Sclerosis Patients Measured by Ultrasound Speckle Tracking Technique
NCT number
NCT03847545
Status
Completed
Phases
Not applicable
Enrollment
48 participants, actual
Lead sponsor
University of Southern Denmark
Conditions
Multiple Sclerosis
Interventions
Fampridine
First posted
2019-02-20
Last updated
2022-04-05

Source ClinicalTrials.gov

Registered outcomes42

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryGait Profile Score (GPS) - (subgroup of 30 allocated to 3D gait analysis)Baseline, 14 days (Change from baseline to 14 days follow-up)
Change in GPS. GPS is a summary measure of kinematic data. The GPS evaluates the overall quality of gait by comparing nine kinematic variables, described as Gait Variable Scores (GVS), relative to normative data. GPS is the root mean square (RMS) difference between the data of relevant kinematic variables of an individual patient and the averaged data from a reference group comprised of people without gait impairments. Originally we had registred that we would use the Gait Deviation Index (GDI). GDI is a unitless value from 0 to 100. It is based upon kinematic data and is an overall quantitative index that summarises the overall gait pathology into a single score for each patient by comparison with non-pathological gait. The GDI and GPS is highly correlated. We chose to use the GPS due to the inclusion of the GVS.
SecondaryGait Variable Scores (GVS) - (subgroup of 30 allocated to 3D gait analysis)Baseline, 14 days (Change from baseline to 14 days follow-up)
Change in GVS. GVS refers to the Root Mean Square difference between the data of the following kinematic variables of an individual patient and the averaged data from a reference group comprised of people without gait impairments: Pelvic tilt, obliquity and rotation; hip flexion-extension, adduction-abduction, and rotation; knee flexion-extension; ankle dorsiflexion; and foot progression.
SecondaryFunctional test - 6 Spot Step Test (SSST)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in time it takes the participant to walk through a rectangular area of 1x 5 meters while 5 cylinder blocks must be kicked out of 5 circles marked on the floor.
SecondaryFunctional test - Timed 25 Footwalk (T25-FW)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in time it takes the participant to walk as safe and as quickly as possible through a straight clearly marked lane of 7.62 meters (25 feet).
SecondaryFunctional test - 2-minute Walk Test (2MWT)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in distance that the participant is able to walk in 2 minutes.
SecondaryWalking speed - (subgroup of 30 allocated to 3D gait analysis)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in walking speed (m/s)
SecondaryStep length - (subgroup of 30 allocated to 3D gait analysis)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in step length (m)
SecondaryStep width - (subgroup of 30 allocated to 3D gait analysis)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in step width (m)
SecondaryStride length - (subgroup of 30 allocated to 3D gait analysis)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in stride length (m)
SecondaryCadence - (subgroup of 30 allocated to 3D gait analysis)Baseline, 14 days (Change from baseline to 14 days follow-up)Change in cadence (steps/min.)

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.

Papers9

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
11687106BACKGROUNDPubMed
17086907BACKGROUNDPubMed
19249634BACKGROUNDPubMed
20976768BACKGROUNDPubMed
21193707BACKGROUNDPubMed
24587826BACKGROUNDPubMed
24852920BACKGROUNDPubMed
27237758BACKGROUNDPubMed
36436320DERIVEDPubMed

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.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT03847545

GET https://conductscience.org/api/trials/v1/NCT03847545/registered?page=2