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Stimulation Change Effects on Quantitative Sensory Testing in Neuromodulation Patients

Primary Purpose

Chronic Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Spinal Cord Stimulator
Sponsored by
Albany Medical College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pain

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Albany Medical Center neurosurgery patients with chronic leg and/or back pain, that have, or are going to have, spinal cord stimulator implantation.
  2. Patients are >/= 18 years old at the time of enrollment.
  3. Patients must be: fluent in English; mentally competent; able to read and answer questionnaires; complete pain assessments; and give informed consent.

Exclusion Criteria:

  1. Patients less than 18 years old.
  2. Patients unable or unwilling to: read and answer questionnaires; complete pain assessments; and give informed consent.

Sites / Locations

  • Albany Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Tonic spinal cord stimulation

Burst spinal cord stimulation

Arm Description

Patients are programmed with tonic (continuous) spinal cord stimulation for a period of four weeks.

Patients are programmed with burst (intermittent) spinal cord stimulation for a period of four weeks.

Outcomes

Primary Outcome Measures

Quantitative Stimulus Testing (QST)-Thermal
Thermal stimulus testing - thermal stimulation system is used to record hot and cold sensation and pain thresholds.

Secondary Outcome Measures

McGill Pain Questionnaire (MPQ)
This outcome measurement tool contains 15 descriptive words (11 sensory and 4 affective) used by subjects to describe their pain. Total number of words chosen is documented
Oswestry Disability Index (ODI)
This measurement tool assesses functional outcome for 10 conditions in subjects with chronic pain. Patients select a statement for each condition that most closely resembles their own situation. Each statement has a score of 0-5, depending on the severity of the particular disability. Raw scores are calculated into a disability percentage.
Beck's Depression Inventory (BDI)
This is a 21 section multiple-choice self-report survey. Patients select a statement in each section that most closely resembles their own situation. Each statement has a score of 0-3, depending on the severity of the depressive content. Raw scores are tallied.
Pain Catastrophizing Scale (PCS)
This is a 13 question survey. It is used to assess the degree to which patients ruminate on, magnify, and/or amplify their pain symptoms. Patients rate on a scale of 0-4 (never - all the time) how often they have each of the thoughts listed. Raw scores are tallied
Numerical Rating Scale (NRS)
Patients rate, on a scale of 0-10, their pain at it's least, most, and average over the past week. They also rate their pain "right now" as well as their perception of Global Improvement.
Epworth Sleepiness Scale (ESS)
This survey is used to assess the 'daytime sleepiness' of patients. Patients rate the likelihood of falling asleep during several daytime scenarios, on a scale of 0-3 (never - very likely). Raw scores are tallied.
Insomnia Severity Index (ISI)
This survey is designed to assess the nature, severity, and impact of insomnia in adults. Patients are asked to rate on a scale of 0-4 (no problem - very much a problem) how much of a problem they have with several sleep conditions. Raw scores are tallied.
Quantitative Stimulus Testing (QST)-Sensitivity
Von Frey fibers are used to determine tactile sensitivity.
Quantitative Stimulus Testing (QST)-Pressure
An algometer is used to measure pain related to pressure.
Quantitative Stimulus Testing (QST)-Vibration
A tuning fork is used to measure sensitivity to vibration.

Full Information

First Posted
July 7, 2020
Last Updated
January 13, 2021
Sponsor
Albany Medical College
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1. Study Identification

Unique Protocol Identification Number
NCT04708392
Brief Title
Stimulation Change Effects on Quantitative Sensory Testing in Neuromodulation Patients
Official Title
Stimulation Change Effects on Quantitative Sensory Testing in Neuromodulation Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
July 29, 2017 (Actual)
Primary Completion Date
July 31, 2018 (Actual)
Study Completion Date
September 11, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Albany Medical College

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
This study is designed to evaluate the effectiveness of two types of spinal cord stimulation programming types, in comparison to each other as well as patient baseline data.
Detailed Description
In this study patients have been implanted with an Abbott spinal cord stimulator capable of delivering both tonic (continuous) stimulation as well as Burst (intermittent) stimulation. Patients are programmed to be in both stimulation modes for a study period of 4 weeks, after which their pain symptoms are evaluated on a variety of surveys: McGill Pain Questionnaire (MPQ), Oswestry Disability Index (ODI), Beck Depression Inventory (BDI), Pain Catastrophizing Scale (PCS), Epworth Sleepiness Scale (ESS), Insomnia Severity Index (ISI), Numerical Rating Scale (NRS) and Global Improvement. They also undergo Quantitative Sensory Testing (QST), where thermal, mechanical, vibration and pressure stimuli are applied to the patient and detection limits are documented.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tonic spinal cord stimulation
Arm Type
Experimental
Arm Description
Patients are programmed with tonic (continuous) spinal cord stimulation for a period of four weeks.
Arm Title
Burst spinal cord stimulation
Arm Type
Experimental
Arm Description
Patients are programmed with burst (intermittent) spinal cord stimulation for a period of four weeks.
Intervention Type
Device
Intervention Name(s)
Spinal Cord Stimulator
Intervention Description
A spinal cord stimulator is a surgically implanted device that delivers an electrical signal to a patient's spinal cord to reduce the perception of pain
Primary Outcome Measure Information:
Title
Quantitative Stimulus Testing (QST)-Thermal
Description
Thermal stimulus testing - thermal stimulation system is used to record hot and cold sensation and pain thresholds.
Time Frame
Change from baseline to 4 weeks
Secondary Outcome Measure Information:
Title
McGill Pain Questionnaire (MPQ)
Description
This outcome measurement tool contains 15 descriptive words (11 sensory and 4 affective) used by subjects to describe their pain. Total number of words chosen is documented
Time Frame
Change from baseline to 4 weeks
Title
Oswestry Disability Index (ODI)
Description
This measurement tool assesses functional outcome for 10 conditions in subjects with chronic pain. Patients select a statement for each condition that most closely resembles their own situation. Each statement has a score of 0-5, depending on the severity of the particular disability. Raw scores are calculated into a disability percentage.
Time Frame
Change from baseline to 4 weeks
Title
Beck's Depression Inventory (BDI)
Description
This is a 21 section multiple-choice self-report survey. Patients select a statement in each section that most closely resembles their own situation. Each statement has a score of 0-3, depending on the severity of the depressive content. Raw scores are tallied.
Time Frame
Change from baseline to 4 weeks
Title
Pain Catastrophizing Scale (PCS)
Description
This is a 13 question survey. It is used to assess the degree to which patients ruminate on, magnify, and/or amplify their pain symptoms. Patients rate on a scale of 0-4 (never - all the time) how often they have each of the thoughts listed. Raw scores are tallied
Time Frame
Change from baseline to 4 weeks
Title
Numerical Rating Scale (NRS)
Description
Patients rate, on a scale of 0-10, their pain at it's least, most, and average over the past week. They also rate their pain "right now" as well as their perception of Global Improvement.
Time Frame
Change from baseline to 4 weeks
Title
Epworth Sleepiness Scale (ESS)
Description
This survey is used to assess the 'daytime sleepiness' of patients. Patients rate the likelihood of falling asleep during several daytime scenarios, on a scale of 0-3 (never - very likely). Raw scores are tallied.
Time Frame
Change from baseline to 4 weeks
Title
Insomnia Severity Index (ISI)
Description
This survey is designed to assess the nature, severity, and impact of insomnia in adults. Patients are asked to rate on a scale of 0-4 (no problem - very much a problem) how much of a problem they have with several sleep conditions. Raw scores are tallied.
Time Frame
Change from baseline to 4 weeks
Title
Quantitative Stimulus Testing (QST)-Sensitivity
Description
Von Frey fibers are used to determine tactile sensitivity.
Time Frame
Change from baseline to 4 weeks
Title
Quantitative Stimulus Testing (QST)-Pressure
Description
An algometer is used to measure pain related to pressure.
Time Frame
Change from baseline to 4 weeks
Title
Quantitative Stimulus Testing (QST)-Vibration
Description
A tuning fork is used to measure sensitivity to vibration.
Time Frame
Change from baseline to 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Albany Medical Center neurosurgery patients with chronic leg and/or back pain, that have, or are going to have, spinal cord stimulator implantation. Patients are >/= 18 years old at the time of enrollment. Patients must be: fluent in English; mentally competent; able to read and answer questionnaires; complete pain assessments; and give informed consent. Exclusion Criteria: Patients less than 18 years old. Patients unable or unwilling to: read and answer questionnaires; complete pain assessments; and give informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julie Pilitsis, MD, PhD
Organizational Affiliation
AMC Department of Neurosurgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Albany Medical Center
City
Albany
State/Province
New York
ZIP/Postal Code
12208
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
28961366
Citation
Deer T, Slavin KV, Amirdelfan K, North RB, Burton AW, Yearwood TL, Tavel E, Staats P, Falowski S, Pope J, Justiz R, Fabi AY, Taghva A, Paicius R, Houden T, Wilson D. Success Using Neuromodulation With BURST (SUNBURST) Study: Results From a Prospective, Randomized Controlled Trial Using a Novel Burst Waveform. Neuromodulation. 2018 Jan;21(1):56-66. doi: 10.1111/ner.12698. Epub 2017 Sep 29.
Results Reference
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PubMed Identifier
27139915
Citation
Hou S, Kemp K, Grabois M. A Systematic Evaluation of Burst Spinal Cord Stimulation for Chronic Back and Limb Pain. Neuromodulation. 2016 Jun;19(4):398-405. doi: 10.1111/ner.12440. Epub 2016 May 3.
Results Reference
background
PubMed Identifier
23321375
Citation
De Ridder D, Plazier M, Kamerling N, Menovsky T, Vanneste S. Burst spinal cord stimulation for limb and back pain. World Neurosurg. 2013 Nov;80(5):642-649.e1. doi: 10.1016/j.wneu.2013.01.040. Epub 2013 Jan 12.
Results Reference
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Stimulation Change Effects on Quantitative Sensory Testing in Neuromodulation Patients

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