[All participants] First assessment session for research purposes only: Participants will
complete the informed consent, VAS pain scale, HIPAA, and medical screening documents. Using
the block randomization method, patients will be randomly assigned to the INF® Therapy only
group or the INF® Therapy+ group by a research coordinator who will not be conducting any
participant assessments. Ten participants will be recruited at a time with five randomly
assigned to each of the two groups. Then all participants will be given brief explanations
before administration of the questionnaires.
Participants will first be instructed to complete the visual analog scale (VAS) for pain, a
subjective measure of pain intensity consisting of a 10-centimeter (cm) line with anchor
statements on the left (no pain) and extreme pain on the right. Pain scores will be
determined by measuring the distance in cm from "no pain" to the participant's anchor point.
Participants who rate their pain level on the visual analog scale (VAS) as greater than seven
out of ten level will be excluded from study participation due to poorly controlled pain.
Next, participants will complete a series of self-report questionnaires beginning with the
CDAT questionnaire which gathers selected information on frequency of purposeful gluten
consumption and self-efficacy to maintain compliance with a gluten-free diet.
The medical screening questionnaire will assess for important comorbid conditions that may
influence outcomes.
Next, the PSQI is a clinical questionnaire assessing quality of sleep and sleep disturbances
over the past month. The 19-item questionnaire provides seven component scores assessing
subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep
disturbance, use of sleep medications, and daytime dysfunction.
Further, the IPAQ-S measures intensity of physical activity and sitting time to estimate
total physical activity per week. Computation of the total score for the short form requires
summation of the duration (in minutes) and frequency (days) of walking, moderate-intensity
and vigorous-intensity activities.
Finally, participants will complete the STAI-form Y which is a definitive clinical measure of
state and trait anxiety in adults. Form Y has 20 items for assessing trait anxiety and 20 for
state anxiety. All items are rated on a 4-point scale (e.g., from "Almost Never" to "Almost
Always"). Higher scores indicate greater anxiety.
All participants will be familiarized to the Neuropad® test and MiniBESTest prior to taking
measurements. The Neuropad® test measures sweat production as an indicator for peripheral
neuropathy severity in people with type 2 diabetes. The time for the cobalt (II) chloride
indicator to complete color change from blue to pink is correlated to severity of nerve
conduction impairment: 892±179 seconds in severe nerve conduction impairment, and 1983±386 in
those with moderate nerve conduction impairment (P =.01). Sudometrics image analysis software
will be utilized to analyze Neuropad® time to color change since it produces continuous
outputs to quantify neuropathic severity. The test will be applied between the first and
second metatarsal bases, avoiding calloused areas after a standard 10-minute prior period
without socks or shoes sitting in a room at a constant 20-25 degrees Celsius. After 10
minutes of test applied, the Neuropad® square will be removed and immediately scanned on a
flatbed scanner to capture the color change result. The image will be analyzed using
Sudometrics software which produces objective continuous outputs to quantify neuropathic
severity.
Next, participants will perform mini balance evaluation system test (Mini-BESTest) which
contains 14 tasks under 4 balance-related subcategories of anticipatory (3 items), reactive
postural control (3 items), sensory orientation (3 items), and dynamic gait (5 items), and
takes approximately 15 minutes to administer. Each item is scored from 0 (unable) to 2
(normal) with a maximum score of 28.
All participants will receive the standard of care INF® Therapy evaluations and treatments
for ten sessions total, two sessions per week (visits two through eleven). During the initial
INF® Therapy evaluation (visit two), three questionnaires will be administered (Background
Information, PQAS, and LENS), and selected data collected for analysis as specified below. An
INF® Therapy treatment will follow the INF® Therapy evaluation.
During INF® Therapy treatment sessions (visits three through ten), either a physical
therapist or physical therapist assistant will provide INF® Therapy treatments. No research
data will be collected during the INF® Therapy treatment sessions.
During the INF® Therapy re-evaluation on visit eleven, the LENS and PQAS questionnaires will
be administered as a post assessment.
[To be completed at initial INF® Therapy evaluation only, visit two] Participants will
complete the Background Information form (self-report) and the following data will be
collected from the form for research purposes as these factors may influence participant
outcomes: participant's gender, smoking, peripheral arterial disease (PAD), hypertension
(HTN), hypercholesteremia, and consumption of the following medications: statins, gabapentin,
or Neurontin.
[To be completed at INF® Therapy initial & re-evaluation, visits two and eleven] The Lower
Extremity Neuropathy Scale (LENS) is a combined assessment including patient report of
sensory and balance disturbances, and clinician-administered, objective assessment of ankle
dorsiflexion strength, vibration and light touch sensitivity, gait mechanics, and balance
during conditions of both static single leg stance and dynamic heel-to-toe pattern during
gait. Use of the LENS is for INF® Therapy PT evaluation only as part of the standard of care.
A separate study for the validation of this tool is in progress. No data from this tool will
be collected for the proposed study.
[To be completed at INF® Therapy initial & re-evaluation, visits two and eleven] The Pain
Quality Assessment Scale (PQAS) is an adjusted version of the validated Neuropathic Pain
Scale and includes 20 pain qualities and descriptors. The tool is validated for detecting
changes in pre-post treatment pain quality and spatial characteristics of pain. Four of the
10 new items showed statistically significant (P .0025) pretreatment to post-treatment
changes, while nine of the items showed at least a moderate effect size (d > .50).12 The
validation study for the original Neuropathic Pain Scale found Pearson correlation
coefficients ranging from .04 to .73.13 The majority of these (39 or 87%) were less than
0.50, indicating minimal overlap (i.e., less than 25% of variance) between most items.13 The
means and standard deviations between items for patients with diabetic neuropathy ranged from
1.76 to 6.54 (2.27 to 3.75) with excellent significance (p < .01).13. [For INF® Therapy+ group only: The clinical therapists will receive training to standardize
the gluten-free dietary (GFD) education to be provided to study participants:
1. Dr. Bussell will conduct an in-service with the clinic's physical therapists and
physical therapist assistants to ensure consistency with GFD education.
2. Therapists will be instructed to review the GFD documents with the participants.
3. The therapists will answer participant questions as appropriate.
During the course of the study: the INF® Therapy+ group will receive individual, face-to-face
standardized verbal dietary education with weekly follow-up by a physical therapist either in
person, via email, or over the phone. The INF® Therapy+ group will additionally receive meal
preparation ideas and sample menus from the Gluten-Free Living website which promotes a
gluten-free lifestyle. A co-investigator not involved in other participant assessments will
complete these tasks] [For all participants] During the first visit, participants will be
instructed verbally and in writing to report any unexpected medical care visits during the
course of the study to the clinic via phone or email prior to any upcoming visits to allow
for processing and re-scheduling. Therapists/student investigator will ask participants at
the beginning of each session if they have had any unexpected visits to the urgent care,
emergency department, physician, or surgeries. Should any adverse or serious adverse events
(AE/SAE) be reported by the participants during enrollment in the study, the participant will
not receive treatment or assessment that day, but be rescheduled.
- - A NTC staff member (Jamie Hankins or Mark Bussell) will notify the student investigator
(Criss Carlson) that same day if an AE or SAE occurs, and the principle investigator
(Eric Johnson) will report the SAE/AE to the IRB in writing within the appropriate time
limits established by the IRB.
- - The principle investigator will notify the NTC in writing if the participant can
continue with treatment or not within 24 to 48 hours.
- - Participants may make up one missed session later in the same week or the following week
after a missed session by receiving three INF® Therapy sessions within a week.
- - If the patient returns and needs to be rescheduled for a second time, the patient will
be dropped from the study.
- - Should any participant miss treatment for more than seven consecutive days, they will be
dropped from the study.
[All participants] Second assessment session for research purposes only (visit 12):
Participants will return the week after completion of the ten INF® Therapy sessions for
immediate post-intervention measurements. Participants will have opportunity to ask any
questions they may have.
[Only for participants in the INF® Therapy+ group: For the INF® Therapy+ group, participants
will be reminded to continue with dietary changes and follow up each week using the CDAT
form. Participants will be contacted weekly by text message, e-mail, or phone call to
facilitate compliance with the dietary changes. The evaluator (PT not involved in other
participant assessments) will either assist participant in completing or review the CDAT
questionnaire that the participant will be instructed to complete prior to the appointment
each week. The weekly CDAT scores will be documented in a spreadsheet maintained separate
from electronic medical records to keep principle evaluator blinded.
In order to accurately assess consistency, it may be ideal to randomly call or text massage
participants by phone (with prior permission) each week with a reminder to complete the
modified CDAT questionnaire.]
[All participants] Final assessment session for research purposes only (visit 13): At the end
of three months post-INF® Therapy completion (10-14 weeks after second assessment),
participants will return for post-intervention measurements. The post-intervention
measurements will include Neuropad® neuropathy severity measure, MiniBESTest functional
balance assessment, visual analog scale (VAS) for pain, the Celiac Dietary Adherence Test
(CDAT), self-reported adherence to dietary changes questionnaire, the Pittsburg Sleep Quality
Index (PSQI), International Physical Activity Questionnaire-short form (IPAQ-S), and
State-Trait Anxiety Inventory Form Y (STAI-form Y).
After the three-month retesting, if a statistically significant difference emerges in the
final analysis, then the INF® Therapy only group will be provided with the same dietary
education materials the INF® Therapy+ group received.
