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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00187863
Other study ID # 61-2005
Secondary ID
Status Completed
Phase N/A
First received September 12, 2005
Last updated March 20, 2015
Start date May 2005
Est. completion date June 2014

Study information

Verified date March 2015
Source University of Florida
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine which factors are associated with the development of chronic shoulder pain and disability.


Description:

The purpose of this study is to determine which factors are associated with the development of chronic shoulder pain and disability. Previous studies have suggested that specific genes influence pain perception. Other studies have suggested that specific psychological factors influence pain perception. We plan to investigate both of these factors to see if they contribute to the development of chronic shoulder pain and disability.


Recruitment information / eligibility

Status Completed
Enrollment 340
Est. completion date June 2014
Est. primary completion date June 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- chronic shoulder pain and disability

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Behavioral:
pain perception
pain perception

Locations

Country Name City State
United States UF Orthopaedics and Sports Medicine Institute Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disability Measurement using the quick DASH Baseline to 12 months No
Primary Pain intensity Measured by the Brief Pain Inventory Baseline to 12 months No
Secondary Physical impairment Measured shoulder range of motion Baseline to 12 months No
Secondary Activity evoked pain Measured by Numerical Rating Scale with shoulder movement Baseline to 12 months No
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