search
Back to results

A Physiologic Comparison of Two Approaches to Treating Peripheral Neuropathy (INF)

Primary Purpose

Peripheral Neuropathy With Type 2 Diabetes

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Intraneural Facilitation Treatment™
Standard Physical Therapy Treatment
Sponsored by
Loma Linda University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Neuropathy With Type 2 Diabetes focused on measuring Intraneural Facilitation, Type 2 Diabetes, Neuropathy, Heart rate variability

Eligibility Criteria

45 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Between the ages of 45 and 85
  • Moderate to severe type II diabetic neuropathy with one or more symptoms including: numbness, tingling, burning, sharp pain, and/or increased sensitivity.
  • Diagnosis confirmed by a physician.
  • Cellphone access with Android 5.0 and up or iOS 14.0 or later.

Exclusion Criteria:

Subjects with a medical condition predisposing them to medical decline during the next 6 months will be excluded from the study. Examples include:

  • Chemotherapy
  • Radiation
  • Lower extremity amputations
  • Open wounds
  • Documented active drug and or alcohol misuse
  • Chronic liver disease
  • Active inflammations
  • Other types of neuropathies not associated with diabetes including B12 deficiency and Charcot Marie Tooth
  • Morbid obesity
  • Pregnancy.
  • Taking beta blockers
  • Unable to maintain steady fingers or operate a cellphone
  • Smoking or ingesting marijuana
  • Having a pacemaker
  • Allergies to cobalt, chrome, or nickel

Sites / Locations

  • Loma Linda University Health Neuropathic Therapy Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Intraneural Facilitation™ Treatment Group

Standard Physical Therapy Treatment Group

Arm Description

Subjects will receive nine 60-minute Intraneural Facilitation™ treatments during sessions 2 through 10. Intraneural facilitation™ is a non-invasive treatment that helps eliminate pain, tingling, numbness, and other symptoms that come with neuropathy.

Subjects will receive nine 60-minute standard physical therapy treatments during sessions 2 through 10.

Outcomes

Primary Outcome Measures

The Impact of INF™ and Standard Physical Therapy on Heart Rate Variability
This is a composite measurement combining electrocardiogram and Welltory App measurements. Heart rate variability (HRV) is the variation in the time interval between consecutive heartbeats and can be used to assess the current state of the nervous system. HRV measures will include LF, HF, LF/HF ratio, SDNN, SDANN, RMSSD, and NN50. The calculation of these variables allows HRV to be quantified. A normal result is between 25 to 50 milliseconds while an abnormal result is less than or greater than that range.

Secondary Outcome Measures

The impact of INF™ and Standard Physical Therapy on neuropathy severity
This will be measured by using ultrasound testing with Neurovascular Index assessment. This is a composite measure of blood flow in the limb. Anterograde and retrograde pulsatility index and volume flow measures are combined to form a mathematical descriptor of the waveform followed by a statistical analysis of variation and then a general score is obtained. A normal result is scored at 250 or less.
The impact of INF™ and Standard Physical Therapy on blood flow
This will be measured by laser doppler flow. Laser Doppler Flowmetry (LDF) is a non-invasive method for measuring changes in microvascular blood perfusion (blood flow) in a variety of tissues. The frequency distribution of the backscattered light is then calculated based on the illumination of the tissue sample. A normal result is relative to the non-affected limb and will be quantified in each patient and compared between visit 2 and 10. An abnormal result would be a 20% or greater reduction in flow in the affected limb.
The impact of INF™and Standard Physical Therapy on inflammation
This will be measured through cytokine levels taken by lab collection. Cytokine levels can vary widely and depend upon current inflammatory state in the patient. C-reactive protein (CRP) is an inflammatory protein that increases with inflammation or infection and can be used as a clinical marker for inflammation. A normal result is < 3mg/L for c-reactive protein. Abnormal result would be levels greater than normal for c-reactive protein.

Full Information

First Posted
September 27, 2022
Last Updated
September 6, 2023
Sponsor
Loma Linda University
search

1. Study Identification

Unique Protocol Identification Number
NCT05577390
Brief Title
A Physiologic Comparison of Two Approaches to Treating Peripheral Neuropathy
Acronym
INF
Official Title
A Physiologic Comparison of Two Approaches to Treating Peripheral Neuropathy
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 2023 (Anticipated)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Loma Linda University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Diabetic peripheral neuropathy is one of the most common and costly microvascular complications of diabetes impacting more than 50% of patients and costing more than 10.1 billion dollars annually. Intraneural facilitation™ (INF) is a non-invasive technique that has shown to improve balance and pain in patients with Type 2 Diabetic Peripheral Neuropathy (T2DPN); however, the underlying physiological mechanisms need further understanding. The purpose of this study is to investigate the physiological mechanisms behind two approaches to treating T2DPN, INF and standard physical therapy. Eligible subjects presenting with diabetic neuropathy symptoms will be recruited and referred to the Loma Linda University Health's Neuropathic Therapy Center. Forty patients will be evenly randomized into two groups: an INF™ treatment group and standard physical therapy treatment group. Subjects will participate in 11 study visits over a period of 6 weeks. Non-invasive assessments will measure neuropathy pain, heart rate variability, neuropathy severity, blood oxygen levels, and blood flow under the skin. Lab draws will measure inflammation levels in the blood and how well blood sugar levels have been maintained over a period of about 3 months. Descriptive statistics and repeated measures ANOVA will be used to analyze data and answer the research questions. The findings of this study will provide a better understanding of how INF™ and standard physical therapy work, subsequently improving non-invasive treatment methods for T2DPN patients.
Detailed Description
Study participants will be assessed on the first, second, fifth, tenth and eleventh sessions. During the participants first and eleventh sessions participants will complete the Pain Quality Assessment Scale (PQAS), the Lower Extremity Neuropathy Scale (LENS), a vascular analysis of the Neurovascular Index (NVI) using a Philips Affinity 50 Ultrasound, and Neuropad® testing. The first session will also include completion of the Background Information form. Patients will be asked to wear loose fitting clothing and to arrive 15 minutes early to complete the informed consent documents on the first session. Welltory App measurements to assess heart rate variability will be taken in the morning and evening the day before, the day of, and the day after each treatment session. On the second session the patient will have: Electrocardiogram testing (ECG) for assessment of heart rate variability (HRV) using PowerLab+LabChart and BioAmp (AD Instruments, Colorado Springs, CO). Near-infrared Spectroscopy (NIRS) measurement using a Foresight Elite monitor (Edwards LifeSciences, Irvine, CA Laser Doppler flowmetry (LDF) measurement using a skin surface Laser Doppler add-on for Chart/Powerlab (AD Instruments, Colorado Springs, CO). Welltory App measurements will be taken before and after treatment to assess for heart rate variability (HRV). A blood draw will be completed by a licensed lab technician to measure blood cytokine and HbA1C levels. A total of 1 1/3 teaspoons of blood will collected at this time point. The blood draw will be performed prior to treatment. The patient will then receive a 60 minute INF™ or standard physical therapy session. The aforementioned tests will then be repeated including ECG, NIRS, and LDF to measure post treatment values. During the third, fourth, sixth, seventh, eighth, and ninth sessions, the patient will have a 60 minute INF™ or standard physical therapy session. Welltory App measurements will be taken before and after treatment to assess for heart rate variability (HRV). On the fifth session the patient will have a 60 minute INF™ or standard physical therapy session. Welltory App measurements will be taken before and after treatment to assess for heart rate variability (HRV). Followed by: • A blood draw by a licensed lab technician to measure blood cytokine levels. A total of 1 ¼ teaspoons will be collected at this time point. On the tenth session the patient will have a 60 minute INF™ or standard physical therapy session. Welltory App measurements will be taken before and after treatment to assess for heart rate variability (HRV). Followed by: Electrocardiogram testing (ECG) for assessment of heart rate variability (HRV) using PowerLab+LabChart and BioAmp (AD Instruments, Colorado Springs, CO). Near-infrared Spectroscopy (NIRS) using a Foresight Elite monitor (Edwards LifeSciences, Irvine, CA Laser Doppler flowmetry (LDF) measurement using a skin surface Laser Doppler add-on for Chart/PowerLab (AD Instruments, Colorado Springs, CO). A blood draw will be completed by licensed lab technician to measure blood cytokine levels and HbA1C. A total of 1 1/3 teaspoons will be collected at this time point.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Neuropathy With Type 2 Diabetes
Keywords
Intraneural Facilitation, Type 2 Diabetes, Neuropathy, Heart rate variability

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Two arms: One INF™ treatment group and One standard physical therapy treatment group
Masking
Investigator
Masking Description
Single-blinded study. Subjects will be randomly assigned to one of two treatment groups. Treating therapists will be informed of the study arm assignment. The physical therapist performing the pre and post evaluation measurements will be different than the treating therapists and blinded to the study arm assignment.
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intraneural Facilitation™ Treatment Group
Arm Type
Experimental
Arm Description
Subjects will receive nine 60-minute Intraneural Facilitation™ treatments during sessions 2 through 10. Intraneural facilitation™ is a non-invasive treatment that helps eliminate pain, tingling, numbness, and other symptoms that come with neuropathy.
Arm Title
Standard Physical Therapy Treatment Group
Arm Type
Experimental
Arm Description
Subjects will receive nine 60-minute standard physical therapy treatments during sessions 2 through 10.
Intervention Type
Other
Intervention Name(s)
Intraneural Facilitation Treatment™
Intervention Description
Intraneural facilitation™ uses three manual holds to bias blood flow to closed endoneurial capillaries. The first is the facilitation hold, which is thought to pressurize the nervous system and bias circulation from the artery into the epineurium. This hold stretches the nerve further than the artery, increasing the amount of elastin in the artery and enlarging the opening of the arterial junction increasing blood into the epineurium. The secondary hold then increases epineurial blood into the transperineurial vessels increasing pressure into the endoneurial capillaries of the site being treated. The third hold, known as the sub hold, encourages blood flow through ischemic endoneurial capillaries that have increased resistance/pressure through the application of Bernoulli's principle. The series of stretches will be repeated on the affected side for the treatment duration.
Intervention Type
Other
Intervention Name(s)
Standard Physical Therapy Treatment
Intervention Description
The standard physical therapy treatment includes muscle stretching, balance, and strengthening exercises known to improve neuropathy symptoms.
Primary Outcome Measure Information:
Title
The Impact of INF™ and Standard Physical Therapy on Heart Rate Variability
Description
This is a composite measurement combining electrocardiogram and Welltory App measurements. Heart rate variability (HRV) is the variation in the time interval between consecutive heartbeats and can be used to assess the current state of the nervous system. HRV measures will include LF, HF, LF/HF ratio, SDNN, SDANN, RMSSD, and NN50. The calculation of these variables allows HRV to be quantified. A normal result is between 25 to 50 milliseconds while an abnormal result is less than or greater than that range.
Time Frame
Through study completion, an average of 6 weeks.
Secondary Outcome Measure Information:
Title
The impact of INF™ and Standard Physical Therapy on neuropathy severity
Description
This will be measured by using ultrasound testing with Neurovascular Index assessment. This is a composite measure of blood flow in the limb. Anterograde and retrograde pulsatility index and volume flow measures are combined to form a mathematical descriptor of the waveform followed by a statistical analysis of variation and then a general score is obtained. A normal result is scored at 250 or less.
Time Frame
Through study completion, an average of 6 weeks.
Title
The impact of INF™ and Standard Physical Therapy on blood flow
Description
This will be measured by laser doppler flow. Laser Doppler Flowmetry (LDF) is a non-invasive method for measuring changes in microvascular blood perfusion (blood flow) in a variety of tissues. The frequency distribution of the backscattered light is then calculated based on the illumination of the tissue sample. A normal result is relative to the non-affected limb and will be quantified in each patient and compared between visit 2 and 10. An abnormal result would be a 20% or greater reduction in flow in the affected limb.
Time Frame
Through study completion, an average of 6 weeks.
Title
The impact of INF™and Standard Physical Therapy on inflammation
Description
This will be measured through cytokine levels taken by lab collection. Cytokine levels can vary widely and depend upon current inflammatory state in the patient. C-reactive protein (CRP) is an inflammatory protein that increases with inflammation or infection and can be used as a clinical marker for inflammation. A normal result is < 3mg/L for c-reactive protein. Abnormal result would be levels greater than normal for c-reactive protein.
Time Frame
Through study completion, an average of 6 weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Between the ages of 45 and 85 Moderate to severe type II diabetic neuropathy with one or more symptoms including: numbness, tingling, burning, sharp pain, and/or increased sensitivity. Diagnosis confirmed by a physician. Cellphone access with Android 5.0 and up or iOS 14.0 or later. Exclusion Criteria: Subjects with a medical condition predisposing them to medical decline during the next 6 months will be excluded from the study. Examples include: Chemotherapy Radiation Lower extremity amputations Open wounds Documented active drug and or alcohol misuse Chronic liver disease Active inflammations Other types of neuropathies not associated with diabetes including B12 deficiency and Charcot Marie Tooth Morbid obesity Pregnancy. Taking beta blockers Unable to maintain steady fingers or operate a cellphone Smoking or ingesting marijuana Having a pacemaker Allergies to cobalt, chrome, or nickel
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mark Bussell, DPT, OCS
Phone
909-558-6799
Email
ntcresearch@llu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Bussell, DPT, OCS
Organizational Affiliation
Loma Linda University Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loma Linda University Health Neuropathic Therapy Center
City
Loma Linda
State/Province
California
ZIP/Postal Code
92350
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark Bussell, DPT, OCS
Phone
909-558-6799
Email
ntcresearch@llu.edu
First Name & Middle Initial & Last Name & Degree
Mark Bussell, DPT, OCS

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All de-identified results and locally developed analysis software will be made available via our laboratory GitHub repository (https://github.com/drcgw/BASS) upon publication of manuscripts from this project. Individual data will be de-identified and combined in a master spreadsheet with subject I.D. numbers. As described in the research protocol, metrics will include data from ultrasound assessments, HRV summary data for each subject, Pulse-doppler, and NIRS data, as well as relevant subject notes that do not include PHI.
IPD Sharing Time Frame
The data will be available indefinitely from six months post-manuscript publication.
IPD Sharing Access Criteria
Data stored on our GitHub repository will be made available to clinicians and researchers after reaching out to the project leaders for access to the data repository.
IPD Sharing URL
https://github.com/drcgw/BASS
Citations:
PubMed Identifier
8737210
Citation
Heart rate variability. Standards of measurement, physiological interpretation, and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Eur Heart J. 1996 Mar;17(3):354-81. No abstract available.
Results Reference
background
PubMed Identifier
31518657
Citation
Saeedi P, Petersohn I, Salpea P, Malanda B, Karuranga S, Unwin N, Colagiuri S, Guariguata L, Motala AA, Ogurtsova K, Shaw JE, Bright D, Williams R; IDF Diabetes Atlas Committee. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th edition. Diabetes Res Clin Pract. 2019 Nov;157:107843. doi: 10.1016/j.diabres.2019.107843. Epub 2019 Sep 10.
Results Reference
background
PubMed Identifier
31197153
Citation
Feldman EL, Callaghan BC, Pop-Busui R, Zochodne DW, Wright DE, Bennett DL, Bril V, Russell JW, Viswanathan V. Diabetic neuropathy. Nat Rev Dis Primers. 2019 Jun 13;5(1):41. doi: 10.1038/s41572-019-0092-1.
Results Reference
background
PubMed Identifier
12766111
Citation
Gordois A, Scuffham P, Shearer A, Oglesby A, Tobian JA. The health care costs of diabetic peripheral neuropathy in the US. Diabetes Care. 2003 Jun;26(6):1790-5. doi: 10.2337/diacare.26.6.1790.
Results Reference
background
PubMed Identifier
16256902
Citation
Gore M, Brandenburg NA, Dukes E, Hoffman DL, Tai KS, Stacey B. Pain severity in diabetic peripheral neuropathy is associated with patient functioning, symptom levels of anxiety and depression, and sleep. J Pain Symptom Manage. 2005 Oct;30(4):374-85. doi: 10.1016/j.jpainsymman.2005.04.009.
Results Reference
background
PubMed Identifier
31456118
Citation
Hicks CW, Selvin E. Epidemiology of Peripheral Neuropathy and Lower Extremity Disease in Diabetes. Curr Diab Rep. 2019 Aug 27;19(10):86. doi: 10.1007/s11892-019-1212-8.
Results Reference
background
PubMed Identifier
31974731
Citation
Callaghan BC, Gallagher G, Fridman V, Feldman EL. Diabetic neuropathy: what does the future hold? Diabetologia. 2020 May;63(5):891-897. doi: 10.1007/s00125-020-05085-9. Epub 2020 Jan 23.
Results Reference
background
PubMed Identifier
26808781
Citation
Alshahrani A, Bussell M, Johnson E, Tsao B, Bahjri K. Effects of a Novel Therapeutic Intervention in Patients With Diabetic Peripheral Neuropathy. Arch Phys Med Rehabil. 2016 May;97(5):733-8. doi: 10.1016/j.apmr.2015.12.026. Epub 2016 Jan 22.
Results Reference
background
PubMed Identifier
23241514
Citation
Sun PC, Kuo CD, Chi LY, Lin HD, Wei SH, Chen CS. Microcirculatory vasomotor changes are associated with severity of peripheral neuropathy in patients with type 2 diabetes. Diab Vasc Dis Res. 2013 May;10(3):270-6. doi: 10.1177/1479164112465443. Epub 2012 Dec 14.
Results Reference
background
PubMed Identifier
33385123
Citation
Zheng H, Sun W, Zhang Q, Zhang Y, Ji L, Liu X, Zhu X, Ye H, Xiong Q, Li Y, Lu B, Zhang S. Proinflammatory cytokines predict the incidence of diabetic peripheral neuropathy over 5 years in Chinese type 2 diabetes patients: A prospective cohort study. EClinicalMedicine. 2020 Dec 23;31:100649. doi: 10.1016/j.eclinm.2020.100649. eCollection 2021 Jan.
Results Reference
background
PubMed Identifier
25281566
Citation
Lockhart CJ, McCann AJ, Pinnock RA, Hamilton PK, Harbinson MT, McVeigh GE. Multimodal functional and anatomic imaging identifies preclinical microvascular abnormalities in type 1 diabetes mellitus. Am J Physiol Heart Circ Physiol. 2014 Dec 15;307(12):H1729-36. doi: 10.1152/ajpheart.00372.2014. Epub 2014 Oct 3.
Results Reference
background
PubMed Identifier
12190997
Citation
McVeigh GE, Morgan DR, Allen P, Trimble M, Hamilton P, Dixon LJ, Silke B, Hayes JR. Early vascular abnormalities and de novo nitrate tolerance in diabetes mellitus. Diabetes Obes Metab. 2002 Sep;4(5):336-41. doi: 10.1046/j.1463-1326.2002.00220.x.
Results Reference
background
PubMed Identifier
30617218
Citation
Selvarajah D, Wilkinson ID, Fang F, Sankar A, Davies J, Boland E, Harding J, Rao G, Gandhi R, Tracey I, Tesfaye S. Structural and Functional Abnormalities of the Primary Somatosensory Cortex in Diabetic Peripheral Neuropathy: A Multimodal MRI Study. Diabetes. 2019 Apr;68(4):796-806. doi: 10.2337/db18-0509. Epub 2019 Jan 7.
Results Reference
background
PubMed Identifier
12716821
Citation
Vinik AI, Maser RE, Mitchell BD, Freeman R. Diabetic autonomic neuropathy. Diabetes Care. 2003 May;26(5):1553-79. doi: 10.2337/diacare.26.5.1553.
Results Reference
background
PubMed Identifier
34309223
Citation
Pop-Busui R, Backlund JC, Bebu I, Braffett BH, Lorenzi G, White NH, Lachin JM, Soliman EZ; DCCT/EDIC Research Group. Utility of using electrocardiogram measures of heart rate variability as a measure of cardiovascular autonomic neuropathy in type 1 diabetes patients. J Diabetes Investig. 2022 Jan;13(1):125-133. doi: 10.1111/jdi.13635. Epub 2021 Aug 14.
Results Reference
background
PubMed Identifier
30292692
Citation
Iannetta D, Inglis EC, Soares RN, McLay KM, Pogliaghi S, Murias JM; CAPES scholarship holder. Reliability of microvascular responsiveness measures derived from near-infrared spectroscopy across a variety of ischemic periods in young and older individuals. Microvasc Res. 2019 Mar;122:117-124. doi: 10.1016/j.mvr.2018.10.001. Epub 2018 Oct 4.
Results Reference
background
PubMed Identifier
15929677
Citation
Brown CD, Davis HT, Ediger MN, Fleming CM, Hull EL, Rohrscheib M. Clinical assessment of near-infrared spectroscopy for noninvasive diabetes screening. Diabetes Technol Ther. 2005 Jun;7(3):456-66. doi: 10.1089/dia.2005.7.456.
Results Reference
background

Learn more about this trial

A Physiologic Comparison of Two Approaches to Treating Peripheral Neuropathy

We'll reach out to this number within 24 hrs