Effects of a Exercise Program on Health Outcomes in People With Diabetic Foot Ulcers
Primary Purpose
Diabetic Foot Ulcer, Diabetes Mellitus, Type 2
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EnhanceFitness community exercise program
Sponsored by
About this trial
This is an interventional prevention trial for Diabetic Foot Ulcer
Eligibility Criteria
Inclusion Criteria:
- 18 or more years of age
- diagnosis of type 2 diabetes
- undergoing treatment for a Wagner grade II, III, or IV diabetic foot ulcer
- able to attend regular exercise classes and two data collection sessions
Exclusion Criteria:
- medical conditions where aerobic or resistance exercise is contraindicated (e.g., uncontrolled cardiovascular problems)
- a score of less than 18 on the Montreal Cognitive Assessment indicating moderate cognitive impairment
- response from primary physician requesting that the participant not engage in exercise
- current participation in a regular exercise program (more than 30 minutes, more than 2 times a week)
Sites / Locations
- Northwest Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Exercise
Control
Arm Description
EnhanceFitness exercise class, 1 hour, 3 times a week, duration of 12 weeks.
Usual care.
Outcomes
Primary Outcome Measures
Glycated Hemoglobin (HbA1c) at 12-week Session
Average blood glucose over a three-month period
Chair Stand Test (5x Sit-to-Stand) at 12-week Session
Measure of functional mobility and lower extremity strength. The 5x Sit-to-Stand test measures the total amount of time that it takes a individual to stand up and sit down in a chair five times. The individual is asked to stand up and sit down five times as quickly as they are able. The research staff started the stopwatch on "begin" and stopped timing after the individual had completed the fifth round of standing/sitting. Faster times are better, and scores are recorded in seconds.
Secondary Outcome Measures
PROMIS-Global at 12-week Session
Patient-Reported Outcome Measurement Information System (PROMIS) Global 10-item short form. Results are reported as a T-score. PROMIS-Global is a self-reported questionnaire to assess global health. T-scores are calculated for 2 subscales- physical health and mental health. A higher T-score indicates better physical health and better mental health; a T-score of 50 indicates the general population mean with a standard deviation of 10. T-scores for physical health range from 16.2 to 67.7. T-scores for mental health range from 21.2 to 67.6.
PROMIS-Depression at 12 Weeks
Patient-Reported Outcome Measurement Information System (PROMIS) Depression 4-item short form. Results are reported as a T-score. PROMIS-Depression is a self-reported questionnaire to assess depression. A higher T-score indicates greater depression; a T-score of 50 indicates the general population mean with a standard deviation of 10. T-scores range from 41.0 to 79.4 for the 4-item short form.
PROMIS-Physical Function
Patient-Reported Outcome Measurement Information System (PROMIS) Physical Function 11-item short form. Results are reported as a T-score. PROMIS-Physical Function is a self-reported questionnaire to assess physical function. A higher T-score indicates better physical function; a T-score of 50 indicates the general population mean with a standard deviation of 10. T-scores range from 11.9 to 57.9 for the 11-item short form.
Retention
Feasibility measure- did the participant attend all study data collection sessions?
Adherence
Feasibility measure- % classes attended by participants in the intervention group
EnhanceFitness Program Evaluation
Feasibility measure, satisfaction with exercise program for participants in the intervention group. This satisfaction measure was designed by EnhanceFitness. It included 5 items, each item was rated by participants as 1 (not at all satisfied) to 5 (very satisfied). Responses for the five questions were summed and divided by 5. Scores ranged from 1-5, with better scored indicating higher satisfaction.
Adverse Events
Feasibility measure- number of adverse events, if any, that occurred for each participant.
Full Information
NCT ID
NCT03002155
First Posted
December 14, 2016
Last Updated
September 29, 2022
Sponsor
University of Washington
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT03002155
Brief Title
Effects of a Exercise Program on Health Outcomes in People With Diabetic Foot Ulcers
Official Title
Effects of a Community Exercise Program on Physical, Physiological, and Psychosocial Health Outcomes in People With Diabetic Foot Ulcers
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
January 2017 (undefined)
Primary Completion Date
June 2018 (Actual)
Study Completion Date
June 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
5. Study Description
Brief Summary
People with diabetes are at risk for life altering complications, including diabetic foot ulcers. To heal a diabetic foot ulcer, people are often required to refrain from bearing weight on their affected limb for months. These long periods of non-weight bearing can result in severe physical deconditioning, putting these individuals at risk for further health decline. The goal of this pilot, randomized controlled trial is to evaluate the effects of a seated exercise program on clinically meaningful outcomes in people with diabetic foot ulcers. The long-term aim of this research is to improve overall health and quality of life in people with complications from diabetes.
Detailed Description
People with diabetes are at risk for life-altering complications and comorbidities. One of the most serious complications is a diabetic foot ulcer, which significantly increases risk for limb amputation. To heal a diabetic foot ulcer, patients are often instructed to refrain from bearing weight on the affected limb. This non-weight bearing protocol results in extended periods of inactivity that can lead to severe physical deconditioning, including diminished strength, endurance, and flexibility. EnhanceFitness, a community exercise program designed for older adults, holds classes that can be adapted for people who are non-weight bearing due to a healing foot ulcer. These exercise classes focus specifically on strength training, aerobic fitness, and stretching - activities that can counteract progressive deconditioning in people with diabetic foot ulcer. Health benefits associated with exercise in people with diabetes are well-established. However, for those experiencing declines in health and physical function because of healing protocols for a diabetic foot ulcer, the potential benefits of exercise are not yet known. The proposed project aims to address this gap in diabetes research.
The long-term goal of this research is to improve the health and quality of life of people with complications from diabetes. The specific goal of this project is to evaluate the effect of a seated community exercise program, EnhanceFitness, on clinically-meaningful outcomes in people with diabetic foot ulcers. Study investigators will recruit people with diabetic foot ulcers from local wound care clinics and randomly assign them to two groups. The first group will engage in EnhanceFitness, an existing community fitness program appropriate for people with weight-bearing restrictions due to wound-healing protocols. The second group will receive the standard of care, which does not include exercise recommendations. To assess the effectiveness of the seated exercise program, the investigators will compare important health outcomes between people with diabetic foot ulcers participating in EnhanceFitness and a control group with diabetic foot ulcers. Specifically, the investigators will assess physical and physiological outcomes, including glycated hemoglobin (HbA1c), lower-extremity strength, and wound healing. The investigators will also measure psychosocial outcomes, such as depression, perceived physical function, overall health, and self-reported ability to continue with exercise. Further, the investigators will evaluate the feasibility of conducting research assessing the effects of seated exercise in people with foot ulcers. The data collected in this pilot research will be used to apply for large, extramural funding that aims to mitigate physical deconditioning in people with diabetic foot ulcers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot Ulcer, Diabetes Mellitus, Type 2
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Exercise
Arm Type
Experimental
Arm Description
EnhanceFitness exercise class, 1 hour, 3 times a week, duration of 12 weeks.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Usual care.
Intervention Type
Other
Intervention Name(s)
EnhanceFitness community exercise program
Other Intervention Name(s)
Seated Exercise, Group exercise, Fitness program
Intervention Description
Level I EnhanceFitness class is a seated fitness class that includes warm up, aerobics, cool down, balance training, strength training, and stretching.
Primary Outcome Measure Information:
Title
Glycated Hemoglobin (HbA1c) at 12-week Session
Description
Average blood glucose over a three-month period
Time Frame
12 weeks post-intervention
Title
Chair Stand Test (5x Sit-to-Stand) at 12-week Session
Description
Measure of functional mobility and lower extremity strength. The 5x Sit-to-Stand test measures the total amount of time that it takes a individual to stand up and sit down in a chair five times. The individual is asked to stand up and sit down five times as quickly as they are able. The research staff started the stopwatch on "begin" and stopped timing after the individual had completed the fifth round of standing/sitting. Faster times are better, and scores are recorded in seconds.
Time Frame
12 weeks post-intervention
Secondary Outcome Measure Information:
Title
PROMIS-Global at 12-week Session
Description
Patient-Reported Outcome Measurement Information System (PROMIS) Global 10-item short form. Results are reported as a T-score. PROMIS-Global is a self-reported questionnaire to assess global health. T-scores are calculated for 2 subscales- physical health and mental health. A higher T-score indicates better physical health and better mental health; a T-score of 50 indicates the general population mean with a standard deviation of 10. T-scores for physical health range from 16.2 to 67.7. T-scores for mental health range from 21.2 to 67.6.
Time Frame
12 weeks post-intervention
Title
PROMIS-Depression at 12 Weeks
Description
Patient-Reported Outcome Measurement Information System (PROMIS) Depression 4-item short form. Results are reported as a T-score. PROMIS-Depression is a self-reported questionnaire to assess depression. A higher T-score indicates greater depression; a T-score of 50 indicates the general population mean with a standard deviation of 10. T-scores range from 41.0 to 79.4 for the 4-item short form.
Time Frame
12 weeks post-intervention
Title
PROMIS-Physical Function
Description
Patient-Reported Outcome Measurement Information System (PROMIS) Physical Function 11-item short form. Results are reported as a T-score. PROMIS-Physical Function is a self-reported questionnaire to assess physical function. A higher T-score indicates better physical function; a T-score of 50 indicates the general population mean with a standard deviation of 10. T-scores range from 11.9 to 57.9 for the 11-item short form.
Time Frame
12 weeks post-intervention
Title
Retention
Description
Feasibility measure- did the participant attend all study data collection sessions?
Time Frame
Through the end of study participation, approximately 12 weeks
Title
Adherence
Description
Feasibility measure- % classes attended by participants in the intervention group
Time Frame
Through the end of study participation, approximately 12 weeks
Title
EnhanceFitness Program Evaluation
Description
Feasibility measure, satisfaction with exercise program for participants in the intervention group. This satisfaction measure was designed by EnhanceFitness. It included 5 items, each item was rated by participants as 1 (not at all satisfied) to 5 (very satisfied). Responses for the five questions were summed and divided by 5. Scores ranged from 1-5, with better scored indicating higher satisfaction.
Time Frame
12-weeks post-intervention
Title
Adverse Events
Description
Feasibility measure- number of adverse events, if any, that occurred for each participant.
Time Frame
Through the end of study participation, approximately 12 weeks
Other Pre-specified Outcome Measures:
Title
Recruitment
Description
Feasibility measure- were overall recruitment targets reached? This feasibility measure will be assessed for the overall study and not for each participant.
Time Frame
At the completion of the 2-year study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 or more years of age
diagnosis of type 2 diabetes
undergoing treatment for a Wagner grade II, III, or IV diabetic foot ulcer
able to attend regular exercise classes and two data collection sessions
Exclusion Criteria:
medical conditions where aerobic or resistance exercise is contraindicated (e.g., uncontrolled cardiovascular problems)
a score of less than 18 on the Montreal Cognitive Assessment indicating moderate cognitive impairment
response from primary physician requesting that the participant not engage in exercise
current participation in a regular exercise program (more than 30 minutes, more than 2 times a week)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sara J Morgan, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwest Hospital
City
Seattle
State/Province
Washington
ZIP/Postal Code
98133
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Effects of a Exercise Program on Health Outcomes in People With Diabetic Foot Ulcers
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