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Trial · NCT07887100

Plantar Fascia Thickness and Pedobarometric Parameters in Sacroiliac Joint Dysfunction

NCT07887100, Completed, Dokuz Eylul University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Plantar Fascia Thickness and Pedobarometric Parameters in Sacroiliac Joint Dysfunction. Trials, record NCT07887100. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07887100

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Trial

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

Title
Plantar Fascia Thickness and Pedobarometric Parameters in Sacroiliac Joint Dysfunction
NCT number
NCT07887100
Status
Completed
Enrollment
52 participants, actual
Lead sponsor
Dokuz Eylul University
Conditions
Sacroiliac Joint Dysfunction, Plantar Fascia Thickness, Pedobarography, Foot Posture Index Score, Pedobarometric
First posted
2026-10-21
Last updated
2026-10-21

Source ClinicalTrials.gov

Registered outcomes9

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

ListOutcomeTime frameDescription
PrimaryPlantar Fascia ThicknessAt enrollment (single assessment visit)
Plantar fascia thickness was measured by ultrasonography in the sagittal plane at the calcaneal insertion of the fascia. Three measurements were taken for each foot, and their mean was recorded in millimeters.
PrimaryCenter of Force Ellipse AreaAt enrollment (single assessment visit)
Center of force (CoF) ellipse area was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded in square centimeters.
PrimaryCenter of Force Path LengthAt enrollment (single assessment visit)
Center of force (CoF) path length was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded in centimeters.
PrimaryCenter of Force VariabilityAt enrollment (single assessment visit)
Center of force (CoF) variability was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded in centimeters.
PrimaryCenter of Force Anteroposterior ExcursionAt enrollment (single assessment visit)
Center of Force Anteroposterior Excursion was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded in centimeters.
PrimaryCenter of Force Mediolateral ExcursionAt enrollment (single assessment visit)
Center of Force Mediolateral Excursion was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded in centimeters.
PrimaryTotal Foot LoadAt enrollment (single assessment visit)
The percentage of body weight borne by each foot was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded as a percentage of body weight.
PrimaryForefoot LoadAt enrollment (single assessment visit)
The percentage of body weight borne by the forefoot region of each foot was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded as a percentage of body weight.
PrimaryRearfoot LoadAt enrollment (single assessment visit)
The percentage of body weight borne by the rearfoot region of each foot was measured with a TekScan MatScan pressure mat under static (eyes open and eyes closed) and dynamic (three-step protocol) conditions. Each measurement was repeated three times, and the mean was recorded as a percentage of body weight.

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.

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/NCT07887100

GET https://conductscience.org/api/trials/v1/NCT07887100/registered