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TerminatedNCT03440008IDCTUpdated Dec 5, 2024Results posted

Improving the Detection, Classification and Treatment of Misaligned Arthritic Ankles

An observational study in Ankle Osteoarthritis, sponsored by VA Office of Research and Development. Terminated at 1 site in United States. Open to participants aged 45 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-12-05.

Sponsored by VA Office of Research and Development · Observational

Why this study was terminated
As a consequence of the COVID-19 pandemic, this study was first paused then ended as the PI moved to a different service line over the course of the VHA's COIVD-19 response.
Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
33
Ages
45 Years to 70 Years
Sex
All
01

Study summary

The Veteran population is prone to foot and ankle maladies from common injuries such as sprains, and diseases such as ankle osteoarthritis (cartilage damage). More specific to Veterans are prior service injuries of the foot and ankle, which historically account for nearly a quarter of injuries received. These injuries include bone fractures and ligament damage. Some of these injuries may lead to poor ankle joint alignment, which over time could lead to osteoarthritis due to abnormal wear on a day to day basis. The goal of this proposal is to use a novel technology - biplane fluoroscopy, to study the movement of ankles which are misaligned in subjects with ankle osteoarthritis. This proposal will also benefit current diagnostic methods with additional information. Last, this proposal will test the effectiveness of a conservative treatment (modified shoe insoles) to correct or reduce the misalignment in ankles. This proposal will create evidence about: the nature of ankle osteoarthritis, the accuracy of diagnosing alignment, and conservative treatment for patients with ankle OA.

Read the detailed description

Ankle osteoarthritis (OA) is a debilitating and mobility limiting condition. It can commonly stem from the result of a traumatic injury - such trauma has a high prevalence in military service. If cartilage is not severely damaged in that trauma, the stability and alignment of the joint may be. Over time, an unstable or misaligned ankle joint can experience abnormal rates of cartilage wear and tear due to aberrant kinematics. While OA may take decades to develop, the resulting arthritic state from this trauma will ultimately require ankle replacement or fusion, consequences with a tremendous financial burden and quality of life impact.

With regards to alignment, particularly in the coronal plane, current clinical diagnosis relies on static X-ray of the ankle joint. Static images may not indicate dynamic misalignment during gait. Further, the effect of wedged insoles, a potential conservative treatment, on the restoration of ankle function is undocumented.

This proposal aims to use biplane fluoroscopy, an X-ray based dynamic imaging approach, to measure ankle kinematics in OA subjects (with varus, neutral and valgus ankle alignment) and controls. With this method, tibio-talar kinematics during gait can be measured. Furthermore, subjects classified as neutral from their static radiograph, but that exhibit ankle varus or valgus alignment during gait, will be identified. Improving the accuracy of a diagnostic outcome provides a patient group with additional avenues for treatment. The investigators will investigate correlations between the investigators' 3D kinematics and clinical 2D imaging - to the benefit of clinical diagnostics. The investigators will also be able to measure the effect of wedged insoles on the restoration of ankle function. With this in mind, the following aims and methodology are proposed.

Specific Aim 1: To investigate ankle kinematics in controls and subjects with OA. In support of Specific Aim 1, 90 ankle OA subjects will be recruited (30 each of varus, neutral or valgus aligned ankles). The investigators will also recruit 20 control subjects. Subjects will receive CT scans of their feet to quantify bone geometry (a step necessary for biplane fluoroscopy). Subjects will then be imaged in the biplane system during gait trials and while wearing neutral study shoes. This will yield tibio-talar kinematics during gait for these populations. Specific Aim 2: To identify dynamically misaligned ankles in OA subjects who are currently classified as neutrally aligned using static analysis. The investigators will compare the static X-ray and the gait kinematics of OA subjects, particularly those with clinically determined neutral alignment. The investigators will determine what proportion of neutral OA subjects actually exhibit misalignment during gait and are thus improperly categorized. The investigators will also re-create 2D clinical X-ray views from the investigators' 3D data in an attempt to translate the investigators' improvement (with 3D fluoroscopy) to more accurately classify alignment to clinical 2D diagnostics. Specific Aim 3: To evaluate the potential of lateral or medial wedging to restore alignment in misaligned ankle OA subjects. OA subjects will be imaged wearing shoes with wedged insoles which correspond to their type of misalignment. Neutral OA subjects, who demonstrate misalignment during gait, will be recalled for a wedged insole session. This yields conservative treatment kinematics.

This study will generate baseline data describing the kinematics of control and ankle OA subjects. This data is not currently available in the literature, and represents a novel contribution to the field. Second, this proposal determines how accurate current 2D X-ray methods are at detecting dynamic misalignment. This information can inform clinicians about the accuracy of their diagnostic tools, and may lead to improvements. Third, this proposal will generate data to evaluate the utility of wedged insoles for the conservative management of ankle misalignment. In Summary, this study has immediate impact potential on the diagnosis and treatment of ankle OA. Last, there are numerous additional avenues of classification, diagnostic, and preventative research for the benefit of the Veterans which will stem from this Career Development Award.

"As a consequence of the COVID-19 pandemic, and after consultation with the appropriate research oversight, regulatory and monitoring entities, screening and enrollment has been placed on temporary administrative hold as of 03/16/2020."

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Conditions studied

  • Ankle Osteoarthritis

Browse trials for

03

Who can participate

Ages eligible
45 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Controls and those with ankle osteoarthritis

Inclusion criteria

  • Be ambulatory (able to walk at least 15 m, and tolerate \~1 hour of standing and walking with rest periods)

Exclusion criteria

Exclusion Criteria:

  • Recent (\<1 year) surgical, neurological, metabolic or lower limb musculoskeletal problem that might impair the ambulation measures in the study

    • Such as severe knee or hip osteoarthritis
  • Diagnosed with diabetes, peripheral neuropathy, or peripheral vascular disease
  • For OA subjects, a radiographic discontinuity of the cartilage of the tibial plafond or talar dome
  • Also for OA subjects, rapid onset of OA (\<3 years) following ankle fracture
  • Diagnosis of severe ankle instability or deformity such as pes planus
  • Inadequate cognitive or language function to consent or to participate
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Study design

Observational model
Cohort
Time perspective
Other
Enrollment
33 participants (actual)
Patient registry
No
Biospecimen retention
None retained

Groups and cohorts

  • Control

    Able-bodied, age matched subjects with no foot and ankle pathology

    Other: Dynamic 3D bone motion capture

  • OA

    Subjects with ankle OA, with all classifications of ankle misalignment (varus, neutral, valgus)

    Other: Dynamic 3D bone motion capture · Device: wedged insole

Interventions

  • OtherDynamic 3D bone motion capture

    Two x-ray systems will image the subjects ankle while they walk, allowing us to calculate ankle joint angle and alignment

    Also known as: Biplane fluoroscopy

  • Devicewedged insole

    medial or lateral wedge (appropriate for varus or valgus misalignment) will be applied during 1 data collection session to evaluate effect of wedging on misalignment

    Also known as: orthotic/insole

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What researchers measure

Primary outcomes

  1. Tibio-talar Kinematics During Gait

    The 3D movement between the tibia and talus bones will be assessed using biplane fluoroscopy, for OA and control subjects during shod gait.

    Time frame: 4 hour session

  2. Static Ankle Alignment Sensitivity

    The sensitivity to correctly diagnose dynamic misalignment by using static x-ray images, will be determined for the OA population.

    Time frame: 4 hour session

  3. Decrease in Misalignment During Gait Using Wedged Insoles

    The effect that wedged insoles have on varus / valgus misalignment will be assessed using dynamic 3D x-ray

    Time frame: 4 hour session

06

Results

Posted Dec 5, 2024

Participant flow

Participants were recruited from a combination of clinician introduction to the study, and posted recruitment materials in 2 hospital systems (VA and academic). The study was open for recruitment in 2016 but due to a laboratory move and hardware update, the first participant was not enrolled until February 2019. The last participant was enrolled in March 2020, three days before a local hold on in-person research was enacted due to the COVID-19 pandemic.

Participant flow — Overall Study
MilestoneControlOA (Osteoarthritis)
Started267
Completed00
Not completed267
Withdrew: Cessation of research visits due to covid-19, pi was transferred to a crisis-response department257
Withdrew: Withdrawal by subject10

Outcome measures

PrimaryTibio-talar Kinematics During Gait

The 3D movement between the tibia and talus bones will be assessed using biplane fluoroscopy, for OA and control subjects during shod gait.

Time frame:
4 hour session

No measurements were reported for this outcome.

PrimaryStatic Ankle Alignment Sensitivity

The sensitivity to correctly diagnose dynamic misalignment by using static x-ray images, will be determined for the OA population.

Time frame:
4 hour session

No measurements were reported for this outcome.

PrimaryDecrease in Misalignment During Gait Using Wedged Insoles

The effect that wedged insoles have on varus / valgus misalignment will be assessed using dynamic 3D x-ray

Time frame:
4 hour session

No measurements were reported for this outcome.

Adverse events

Collected over No participants performed any study visits (e.g. for Primary Outcome 1-3), therefore there were no periods of time over which AE, SAE, or UAPs could be collected.. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Control———
OA (Osteoarthritis)———

Baseline characteristics

Age, Continuous
Age, Continuous(Years)ControlOA (Osteoarthritis)Total
Mean59.0 (41 to 78)55.4 (38 to 68)58.2 (38 to 78)
Sex: Female, Male
Sex: Female, Male(Participants)ControlOA (Osteoarthritis)Total
Female12012
Male13720
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)ControlOA (Osteoarthritis)Total
Hispanic or Latino202
Not Hispanic or Latino23528
Unknown or Not Reported022
Race (NIH/OMB)
Race (NIH/OMB)(Participants)ControlOA (Osteoarthritis)Total
American Indian or Alaska Native101
Asian000
Native Hawaiian or Other Pacific Islander011
Black or African American606
White17421
More than one race101
Unknown or Not Reported022
Region of Enrollment
Region of Enrollment(Participants)ControlOA (Osteoarthritis)Total
United States25732
Varus/Neutral/Valgus Alignment
Varus/Neutral/Valgus Alignment(Participants)ControlOA (Osteoarthritis)Total
Varus Misaligned000
Neutral Alignment000
Valgus Misaligned000
Unknown Alignment25732
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Study locations

1 site
  • VA Puget Sound Health Care System Seattle Division, Seattle, WA
    Seattle, Washington 98108, United States
08

References and documents

Study documents

  • Protocol and statistical analysis plan · Dec 9, 2020

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Registry details

Key details

Study ID
NCT03440008
Lead sponsor
VA Office of Research and Development
Responsible party
Sponsor
First posted
Feb 20, 2018
Start date
Dec 22, 2016
Primary completion
Mar 10, 2020
Completion
Nov 16, 2023
Results posted
Dec 5, 2024
Last update
Dec 5, 2024

Study contacts

Joseph Iaquinto, PhD
principal investigator · VA Puget Sound Health Care System Seattle Division, Seattle, WA

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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