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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01040962
Other study ID # 11481
Secondary ID GCRC Protocol #0
Status Completed
Phase N/A
First received December 28, 2009
Last updated June 15, 2012
Start date August 2008
Est. completion date December 2010

Study information

Verified date June 2012
Source University of Kansas Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Fall risk is increased in people with diabetic peripheral neuropathy (DPN) and yet, minimal research has been conducted to identify appropriate fall risk assessment tools and improve our understanding of falls in these individuals. Purpose: The primary purpose of this study is to establish a foundation of knowledge needed to address falls in people with DPN. This will be accomplished through 1) comparing the validity of 4 fall risk assessment tools, 2) identifying risk factors for falls and 3) determining how quality of life is influenced by factors related to falls in people with DPN.


Description:

All subjects participate in testing that involves questionnaires, cognitive testing, fall risk assessment, and other testing related to physical parameters including body mass index, glycosylated hemoglobin, lower extremity nerve conduction study, and ankle range of motion, proprioception and strength. After testing, subjects are interviewed to determine fall status (faller or non-faller). A "faller" is defined as someone that has fallen at least 2 times in the past year. Data Analysis: The validity of the fall risk assessment tools will be compared using sensitivity and specificity analyses. Variables related to ankle function, neuropathy, glycemic control and general activity will be analyzed for association with recent fall history through multivariable logistic regression. Variables related to falls, neuropathy and activity level will be analyzed for association with health-related quality of life through multivariable linear regression.


Recruitment information / eligibility

Status Completed
Enrollment 37
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria:

- diagnosed with diabetic peripheral neuropathy

Exclusion Criteria:

- major medical depression

- non-diabetes related musculoskeletal problems that limit ambulation

- open wounds on the weight bearing surfaces of the feet

- requires another person's assistance to walk

- uncorrected visual deficits that influence gait and/or balance

- history of stroke or other CNS pathology that impairs gait and/or balance

- diagnosed untreated vestibular disorder that results in gait and/or balance disturbances

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
United States North Kansas City Hospital Kansas City Missouri
United States University of Kansas Medical Center Kansas City Kansas

Sponsors (1)

Lead Sponsor Collaborator
Stephen D. Jernigan, PT, PhD

Country where clinical trial is conducted

United States, 

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