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Effect of Weight-Bearing Exercise on People With Diabetes and Neuropathic Feet

Primary Purpose

Diabetes Mellitus, Peripheral Neuropathy

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
weightbearing exercise
nonweightbearing exercise
nonexercising control
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetes Mellitus focused on measuring diabetes mellitus, peripheral neuropathy, exercise

Eligibility Criteria

40 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 1 or Type 2 DM and PN
  • biothesiometer > 25mV and
  • unable to sense the 5.07 Semmes Weinstein monofilament on at least one spot on the plantar foot
  • Relatively sedentary
  • step count of 2-9,000 steps per day
  • exercising less than 3 times per week (<20 min/session).
  • Have the approval of his/her primary care physician to participate in the study.

Exclusion Criteria:

  • Subjects who weigh greater than 300 pounds (DXA scanner's weight limit).
  • A history of severe foot deformity, such as Charcot neuroarthropathy or partial foot amputation that would require custom therapeutic footwear.
  • Any co-morbidity or medication that would interfere with ability to exercise according to ADA and ACSM guidelines.
  • People with severe depression as determined by the Beck Depression Inventory II with a score of 29 or greater.
  • People who are physically incapable of tolerating one hour of activity.
  • Women of child bearing age due to risk of exposure from radiation in DXA testing.

Sites / Locations

  • Program in Physical Therapy, Washington University in St. Louis

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Placebo Comparator

Experimental

Arm Label

nonweightbearing exercise

nonexercising control

weightbearing exercise

Arm Description

Outcomes

Primary Outcome Measures

daily step count

Secondary Outcome Measures

skin breakdown

Full Information

First Posted
September 26, 2008
Last Updated
November 3, 2017
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00763087
Brief Title
Effect of Weight-Bearing Exercise on People With Diabetes and Neuropathic Feet
Official Title
Effect of Weight-Bearing Exercise on People With Diabetes and Neuropathic Feet
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
January 2011 (Actual)
Study Completion Date
January 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if people with Diabetes Mellitus and peripheral neuropathy can increase their activity (i.e. walking or stationary biking) and leg strength without having an increase in foot problems compared to a group of people with diabetes and peripheral neuropathy that do no exercise. Our hypothesis is that the weight-bearing exercise group will achieve greater increases in weight-bearing activity (i.e., increased steps/day and cumulative load) and leg strength compared to the non-weight bearing exercise group and the non-exercising control group; and there will be no clinically meaningful difference in incidence or indicators of foot lesions between groups.
Detailed Description
People with diabetes and peripheral neuropathy (DM+PN) have substantial lower extremity impairments, functional limitations and disability. In addition to muscle weakness and poor balance, they also are at high risk for foot ulcerations, especially if they have a history of ulceration. Although there is a large and growing body of knowledge about the effect of exercise on people with DM, there is little evidence about the effect of exercise in people with DM+PN. Exercise is an important treatment component to help control the complications of DM. The American Diabetes Association (ADA), and the American College of Sports Medicine (ACSM)4 recommend that adults with DM participate in at least 30 minutes a day of moderate-intensity physical activity that is consistent with a brisk walk. The ADA and ACSM, however, discourage weight-bearing exercise for people with DM+PN due to risk of exercise-induced foot injury. No data support this guideline to restrict those with DM+PN from weight-bearing activity, and in fact, some evidence suggests that those with DM+PN who are most active are least likely to develop skin breakdown. The Primary Goal of this proposal is to conduct a pilot randomized prospective controlled clinical trial to determine if people with DM+PN can benefit from a progressive weight-bearing exercise program to improve impairments, functional limitations, disability, and pathophysiology without an increase in skin breakdown or foot lesions. The benefits of a weight bearing program will be compared to the benefits of a non weight bearing exercise program and to a non-exercising control group. The results of this study also will help to determine if neuropathic skin and muscle can adapt to increasing physical stress levels without injury which could have important implications for weight-bearing and exercise guidelines for people with DM+PN. A. SPECIFIC AIMS Aim 1. Determine the effect of a weight-bearing exercise program compared to a non-weight bearing exercise program and to a non-exercising control group on indicators of impairments, functional limitations, disability, and pathophysiology in patients with DM+PN. Measures of Impairment: Ankle joint range of motion, ankle plantar flexor and dorsiflexor muscle strength (peak torque), muscle volume (magnetic resonance imaging), and standing balance. H1: Both exercise groups will show an improvement in ankle joint range of motion and ankle plantar flexor / dorsiflexor muscle strength / volume compared to the non-exercising control group, but only the weight-bearing exercise group will show an improvement in standing balance because of exposure to challenging weight-bearing activities. Measures of Functional Limitations: Physical Performance Test, Foot & Ankle Ability Measure. H2: Both exercise groups will show improvement in the Physical Performance Test and Foot & Ankle Ability Measure compared to the non-exercising control group, and the weight-bearing exercise group will show greater improvements than the non-weight bearing exercise group because of improved balance and exposure to challenging weight-bearing activities. Measures of Disability / Participation: Diabetes Symptom Checklist, Beck Depression Inventory. H3: Both exercise groups will show improved measures of disability compared to the non-exercising control group, and the weight-bearing exercise group will show greater improvements than the non-weight bearing exercise group because of improved ability to participate in community activities which require weight-bearing and walking ability. Measures of Pathophysiology: HbA1c, serum lipids, DXA (body composition), and body mass index. H4: Both exercise groups will show modest but statistically significant improvements compared to the non-exercising control group in the above measures of pathophysiology. Aim 2: Determine the effect of weight-bearing exercise program and non-weight bearing exercise program compared to a control group on 1) daily step count (steps/day), 2) an estimate of cumulative load (step count * plantar pressure integral), 3) unilateral increase in surface foot temperature, and 4) incidence of foot lesions (digital photograph). H5: The weight-bearing exercise group will achieve greater increases in weight-bearing activity (i.e., increased steps/day and cumulative load) compared to the non-weight bearing exercise group and the non-exercising control group; and there will be no clinically meaningful difference in incidence or indicators of foot lesions between groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Peripheral Neuropathy
Keywords
diabetes mellitus, peripheral neuropathy, exercise

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
43 (Actual)

8. Arms, Groups, and Interventions

Arm Title
nonweightbearing exercise
Arm Type
Active Comparator
Arm Title
nonexercising control
Arm Type
Placebo Comparator
Arm Title
weightbearing exercise
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
weightbearing exercise
Intervention Description
All subjects in the exercise group will participate, as able, in 3 supervised 1 hour exercise sessions per week for the first month and 2 supervised and 1 unsupervised exercise session per week for the remaining 2 months. Subjects in each exercise group will be seen on alternating times to avoid cross contamination of treatment intervention. Walking intensity for all subjects will be applied with the intent to exceed their routine physical stress level, and therefore incur positive adaptations to physical stress, but not exceed their threshold for injury.
Intervention Type
Behavioral
Intervention Name(s)
nonweightbearing exercise
Intervention Description
All subjects in the 2 exercise groups will participate, as able, in 3 supervised 1 hour exercise sessions per week for the first month and 2 supervised and 1 unsupervised exercise session per week for the remaining 2 months. Subjects in each exercise group will be seen on alternating times to avoid cross contamination of treatment intervention. Biking intensity for all subjects will be applied with the intent to exceed their routine physical stress level, and therefore incur positive adaptations to physical stress, but not exceed their threshold for injury.
Intervention Type
Behavioral
Intervention Name(s)
nonexercising control
Intervention Description
All subjects will be instructed, verbally and with written documents, regarding appropriate foot and skin care twice per month.
Primary Outcome Measure Information:
Title
daily step count
Time Frame
3 months
Secondary Outcome Measure Information:
Title
skin breakdown
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 1 or Type 2 DM and PN biothesiometer > 25mV and unable to sense the 5.07 Semmes Weinstein monofilament on at least one spot on the plantar foot Relatively sedentary step count of 2-9,000 steps per day exercising less than 3 times per week (<20 min/session). Have the approval of his/her primary care physician to participate in the study. Exclusion Criteria: Subjects who weigh greater than 300 pounds (DXA scanner's weight limit). A history of severe foot deformity, such as Charcot neuroarthropathy or partial foot amputation that would require custom therapeutic footwear. Any co-morbidity or medication that would interfere with ability to exercise according to ADA and ACSM guidelines. People with severe depression as determined by the Beck Depression Inventory II with a score of 29 or greater. People who are physically incapable of tolerating one hour of activity. Women of child bearing age due to risk of exposure from radiation in DXA testing.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael J Mueller, PT, PhD
Organizational Affiliation
Washington University in St. Louis, Program in Physical Therapy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Program in Physical Therapy, Washington University in St. Louis
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63108
Country
United States

12. IPD Sharing Statement

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Effect of Weight-Bearing Exercise on People With Diabetes and Neuropathic Feet

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