Examining Effects of Aerobic Exercise on Pain Sensation

September 26, 2019 updated by: University of Kansas Medical Center

Phenotyping Chronic Low Back Pain Patients With Central Sensitization

By doing this study, researchers hope to learn effects of aerobic exercise on over activated nervous system in people with chronic low back pain.

Study Overview

Status

Completed

Detailed Description

Chronic low back pain is a common condition in the world. About 85% of people with low back pain do not know the cause of their pain. This leads to ineffective treatments.

Recently, the idea of an over activated nervous system is thought to be one of the main reasons for chronic pain. Over activated nervous system means pain processing areas in the spine or brain might be more sensitive. Aerobic exercise, such as walking and cycling, is often used to decrease chronic pain. Aerobic exercise is a form of physical exercise that strengthen the heart and lungs in order to improve the body's utilization of oxygen.

The researchers want to examine if aerobic exercise is effective in decreasing over activation of the nervous system. Gaining a better understanding of effects of aerobic exercise on the nervous system may lead to more effective treatments for low back pain.

Study Type

Interventional

Enrollment (Actual)

10

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kansas
      • Kansas City, Kansas, United States, 66160
        • University of Kansas Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Lower back pain (LBP) for more than 3 months
  • A minimal pain level of 3 on the 0-10 pain numerical rating scale (NRS) in the last 7 days
  • Can read and understand English.

Exclusion Criteria:

  • Nerve root compression that resulted in numbness or decrease in sensation in the areas for the pain sensitivity tests as reported by the subject
  • cervical or thoracic pain as a main complaint
  • spinal pathologies such as fracture, tumor, infection, and severe inflammation
  • severe spinal deformity
  • severe cardiovascular and neurological diseases
  • cancer
  • history of spinal surgery
  • currently seeking active treatments for LBP other than medications
  • resting blood pressure more than 160/90 mmHg 49
  • currently taking blood thinning medications
  • uncontrolled diabetes
  • cannot have blood pressure taken
  • participated in a similar trial in the past

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Aerobic exercise program
Participants will complete 12 week exercise program.
Exercise program consists of training for 60 minutes, three times per week for 12 weeks. Participants will use a treadmill, Nu stepper/bike or elliptical to exercise.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain sensitivity (Pressure pain threshold)
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Sensitivity will be measured using a pressure algometer.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
2011 FM survey
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Sensitivity will be measured using the 2011 Fibromyalgia (FM) Survey Criteria. The survey includes widespread pain index and symptom severity scale. The total score is 31 and scores more than 13 is considered fibromyalgia positive, suggesting presence of central sensitization.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Opioid consumption
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Use of opioids (dose, frequency, and duration) will be obtained by interviewing the subjects
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Oswestry Disability Index
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
This questionnaire consists of questions related to daily functions and degrees to which back pain interferes with these functions. Each items is measured on a 6-point scale with a total possible score of 50. Higher numbers indicate greater disability.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain Sensitivity (CPM test)
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Measure of the functionality of descending inhibitory pain pathways with use of pressure algometry.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Fear Avoidance Belief Questionnaire
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
The survey has items related to fear about physical and work activities. Each item is scored from 0-6 points, with higher number indicating increased fear of activity or work.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Pain Catastrophizing Scale
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
PCS is a validated 13--item scale with questions related to catastrophizing behavior. Total score is 52 with higher scores indicating greater catastrophic thoughts.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Beck Depression Inventory
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Beck depression questionnaire contains 21 multiple-choice depression related questions on a scale value of 0 to 3. Higher scores indicate greater depressive symptoms.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Beck Anxiety Inventory
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Beck anxiety questionnaire contains 21 multiple-choice questions, each score 0 (not al all) to 3 (severely). Higher scores indicate greater anxiety symptoms.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Pittsburgh Sleep Quality Index
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Pittsburgh sleep quality index contains 19 questions, creating 7 components that produce one global score. Higher scores indicate poorer sleep quality.
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Lumbar spine range of motion
Time Frame: Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)
Lumbar spine range of motion into forward, backward, and side bending will be assessed with two inclinometers or a tape measure. subjects will
Change from Baseline (pre-treatment) to after completion of 3 months of aerobic exercise training (post-treatment)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Neena Sharma, PT, PhD, CMPT, University of Kansas Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2018

Primary Completion (Actual)

September 1, 2019

Study Completion (Actual)

September 1, 2019

Study Registration Dates

First Submitted

May 22, 2018

First Submitted That Met QC Criteria

June 1, 2018

First Posted (Actual)

June 6, 2018

Study Record Updates

Last Update Posted (Actual)

September 27, 2019

Last Update Submitted That Met QC Criteria

September 26, 2019

Last Verified

September 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • STUDY00141062

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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