Trial · NCT07895602
Effects of Custom 3D Printed Insoles and Short Foot Exercises in Pes Planus
NCT07895602, Not applicable, Recruiting, Kutahya Health Sciences University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of Custom 3D Printed Insoles and Short Foot Exercises in Pes Planus. Trials, record NCT07895602. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07895602
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of Custom 3D Printed Insoles and Short Foot Exercises in Pes Planus
- NCT number
- NCT07895602
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 54 participants, estimated
- Lead sponsor
- Kutahya Health Sciences University
- Conditions
- Pes Planus
- Interventions
- Custom 3D Printed Insoles and Short Foot Exercises
- First posted
- 2026-10-26
- Last updated
- 2026-11-05
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Foot Posture Index-6 (FPI-6) | Baseline and 8 Weeks | Assesses foot posture across 6 criteria. Total scores range from -12 (highly supinated) to +12 (highly pronated). |
| Primary | Navicular Drop Test (NDT) | Baseline and 8 Weeks | Assesses medial longitudinal arch height difference (in mm) between seated (non-weight bearing) and standing (weight bearing) positions. Higher values indicate increased pronation. |
| Primary | Modified Star Excursion Balance Test (MSEBT) | Baseline and 8 Weeks | Evaluates dynamic balance by measuring the maximum reach distance (in cm) in three directions: anterior, posteromedial, and posterolateral. |
| Primary | Spatiotemporal Gait and Plantar Pressure Parameters | Baseline and 8 Weeks | Evaluated using the Zebris system. Includes gait speed (m/s), cadence (steps/min), stride length (cm), stance percentage (%), and plantar pressure parameters (e.g., peak pressure, contact area). |
| Secondary | Numeric Pain Rating Scale (NPRS) | Baseline and 8 Weeks | Assesses pain intensity on an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain). |
| Secondary | 36-Item Short Form Health Survey (SF-36) | Baseline and 8 Weeks | Assesses health-related quality of life across 8 domains. Subscale scores are transformed to a 0 to 100 scale, where higher scores indicate better health status. |
| Secondary | 6-Minute Walk Test (6MWT) and Modified Borg Scale | Baseline and 8 Weeks | Evaluates functional capacity by measuring the total distance walked in 6 minutes (in meters). Perceived exertion is assessed before and after the test using the Modified Borg Scale (0-10 scale; higher scores indicate greater exertion). |
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.
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.
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/NCT07895602
GET https://conductscience.org/api/trials/v1/NCT07895602/registered