Reliability and Validity of Goniometric iPhone Applications

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Texas Woman's University
ClinicalTrials.gov Identifier:
NCT01629641
First received: June 18, 2012
Last updated: June 26, 2012
Last verified: June 2012
  Purpose

The purpose of this study is to determine the test-retest and inter-rater reliability and concurrent validity of two iPhone goniometric applications in the measurement of active shoulder external rotation as compared to a standard manual goniometer. The scientific hypotheses for this study are as follows:

  1. There will be significant Pearson correlations (>.8) to demonstrate test-retest reliability for each of the tools between the 1st and 2nd round of testing as assessed by novice testers.
  2. There will be significant intra-class correlation coefficients (>.8) to demonstrate inter-rater reliability between the novice tester and the experienced tester for each of the three tools.
  3. There will be significant Pearson correlations (>.8) to demonstrate concurrent validity between the standard goniometer and the photo capture application, the standard goniometer and the accelerometer-based application and the photo capture application with the accelerometer-based app. as assessed by novice testers.

Condition
Shoulder Pain

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Reliability and Validity of Goniometric iPhone Applications for the Assessment of Active Shoulder External Rotation

Further study details as provided by Texas Woman's University:

Primary Outcome Measures:
  • Active Shoulder External Rotation Range of Motion [ Designated as safety issue: No ]
    Range of Motion will be collected via two iPhone applications and a standard goniometer.


Enrollment: 94
Study Start Date: January 2012
Study Completion Date: March 2012
Primary Completion Date: January 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
Normals
Texas Woman's University students from the School of Physical Therapy - Houston campus will be recruited to participate in this study. The participant will be excluded if they have pain in the shoulder on the day of testing, less than 90 degrees of active or passive shoulder abduction, less than 90 degrees of active or passive elbow flexion, have had any previous surgeries or procedures to either shoulder or identify by self-report any reason that they should not perform active external rotation at the shoulder.

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   20 Years to 50 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Texas Woman's University students from the School of Physical Therapy - Houston campus will be recruited to participate in this study.

Criteria

Inclusion Criteria:

  • Current graduate student at Texas Woman's University. Must be enrolled in the DPT graduate program in Physical Therapy at the Houston campus.

Exclusion Criteria:

  • The participant will be excluded if they have pain in the shoulder on the day of testing, less than 90 degrees of active or passive shoulder abduction, less than 90 degrees of active or passive elbow flexion, have had any previous surgeries or procedures to either shoulder or identify by self-report any reason that they should not perform active external rotation at the shoulder.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01629641

Locations
United States, Texas
Texas Woman's University
Houston, Texas, United States, 77030
Sponsors and Collaborators
Texas Woman's University
Investigators
Principal Investigator: Katy Mitchell, PT, PhD Texas Woman's University
  More Information

No publications provided

Responsible Party: Texas Woman's University
ClinicalTrials.gov Identifier: NCT01629641     History of Changes
Other Study ID Numbers: 17008
Study First Received: June 18, 2012
Last Updated: June 26, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by Texas Woman's University:
goniometry
outcome measures
shoulder assessment

Additional relevant MeSH terms:
Shoulder Pain
Arthralgia
Joint Diseases
Musculoskeletal Diseases
Pain
Signs and Symptoms

ClinicalTrials.gov processed this record on July 22, 2014