Trial · NCT07889765
Comparative Effect of Training Methods to Reduce Forefoot Loading in Carbon Fiber Custom Dynamic Orthoses
NCT07889765, Not applicable, Recruiting, Jason Wilken
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparative Effect of Training Methods to Reduce Forefoot Loading in Carbon Fiber Custom Dynamic Orthoses. Trials, record NCT07889765. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889765
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparative Effect of Training Methods to Reduce Forefoot Loading in Carbon Fiber Custom Dynamic Orthoses
- NCT number
- NCT07889765
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 51 participants, estimated
- Lead sponsor
- Jason Wilken
- Conditions
- Healthy
- Interventions
- Carbon Fiber Custom Dynamic Orthosis
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Peak Forefoot Force | Baseline | Peak plantar forces, normalized to body mass (N/kg) will be measured across the forefoot (distal 40% of sensor). |
| Primary | Forefoot Force Impulse | Baseline | Plantar force impulse, normalized to body mass (Ns/kg) across the forefoot (distal 40% of sensor) will be calculated using the integral of the force over the stance phase. |
| Secondary | Peak Midfoot Force | Baseline | Peak plantar forces, normalized to body mass (N/kg) will be measured across the midfoot (middle 30% of sensor). |
| Secondary | Midfoot Force Impulse | Baseline | Plantar force impulse, normalized to body mass (Ns/kg) across the midfoot (middle 30% of sensor) will be calculated using the integral of the force over the stance phase. |
| Secondary | Peak Hindfoot Force | Baseline | Peak plantar forces, normalized to body mass (N/kg) will be measured across the hindfoot (proximal 30% of sensor). |
| Secondary | Hindfoot Force Impulse | Baseline | Plantar force impulse, normalized to body mass (Ns/kg) across the hindfoot (proximal 30% of sensor) will be calculated using the integral of the force over the stance phase. |
| Secondary | Peak Total Foot Force | Baseline | Peak plantar forces, normalized to body mass (N/kg) will be measured across the total foot (100% of sensor). |
| Secondary | Total Foot Force Impulse | Baseline | Plantar force impulse, normalized to body mass (Ns/kg) across the total foot (100% of sensor) will be calculated using the integral of the force over the stance phase. |
| Other | Numerical Pain Rating Scale | Baseline | Pain will be assessed using a standard 11-point numerical pain rating scale, in which 0 = no pain and 10 = worst pain imaginable |
| Other | Modified Socket Comfort Score (Comfort) | Baseline | Comfort scores range from 0 = most uncomfortable to 10= most comfortable |
1 to 10 of 11Source ClinicalTrials.gov
See all 11 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.
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/NCT07889765
GET https://conductscience.org/api/trials/v1/NCT07889765/registered