Effects of Different Instrument Assisted Soft Tissue Mobilization Force Applications on Ankle Stiffness and Dorsiflexion
NCT07927179, Not applicable, Not yet recruiting, University of Idaho
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effects of Different Instrument Assisted Soft Tissue Mobilization Force Applications on Ankle Stiffness and Dorsiflexion | ClinicalTrials.gov |
| NCT number | NCT07927179 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 45 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | University of Idaho | ClinicalTrials.gov |
| Conditions | Range of Motion, Articular, Ankle Joint, High Force IASTM Treatment, Low Force IASTM Treatment, Control Condition With no Treatment | ClinicalTrials.gov |
| Interventions | Instrument Assisted Soft Tissue Mobilization | ClinicalTrials.gov |
| First posted | 2026-11-10 | ClinicalTrials.gov |
| Last updated | 2026-11-10 | ClinicalTrials.gov |
Registered outcomes 2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Change in Weight Bearing Ankle Dorsiflexion Range of Motion | Baseline and immediately after the intervention or control condition (within 30 minutes, same session) | Ankle dorsiflexion is the ability to bend the ankle so the shin moves forward over the foot. It is measured with the Weight Bearing Lunge Test. The participant stands in a split stance, keeps the back heel on the floor, and bends the front knee forward as far as possible until the front heel begins to lift. An inertial measurement unit (a small motion sensor) on the shin records the angle of the shin relative to vertical at the moment the heel lifts. \[Confirm this is how the angle is derived.\] Each leg is tested 3 times, and the mean of the 3 trials is used. Values are reported in degrees, and higher values indicate greater ankle mobility. Change is calculated as the post-treatment value minus the baseline value | ClinicalTrials.gov |
| Primary | Change in Dynamic Stiffness of the Calf Muscles, Achilles Tendon, and Plantar Fascia | Baseline and immediately after the intervention or control condition (within 30 minutes, same session) | Tissue stiffness is measured with the MyotonPRO (Myoton AS, Tallinn, Estonia). This handheld device applies a brief, painless mechanical tap to the skin and records how the underlying tissue oscillates in response. Participants lie face down on an examination table with a foam roller under the front of the ankles to keep the knees slightly bent and the legs relaxed. The probe is held perpendicular to the skin. | 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 |
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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 3
The papers the trial lists on ClinicalTrials.gov.
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 0
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 |
|---|
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)