Reliability and Validity of iPhone Application for OBER
Concurrent Validity and Reliability of the iPhone® Measurement Application to Evaluate Iliotibial Band Length
1 other identifier
interventional
30
1 country
1
Brief Summary
The validity and reliability of adduction angle measurement of hip with smartphone will be investigate.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 4, 2021
CompletedStudy Start
First participant enrolled
March 8, 2021
CompletedFirst Posted
Study publicly available on registry
March 9, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 24, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
April 26, 2021
CompletedSeptember 8, 2021
March 1, 2021
2 months
March 4, 2021
September 7, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
iPhone Measurement Application
Iliotibial band length of the participants will be measured with the iPhone Measurement Application
3 weeks
Secondary Outcomes (1)
Bubble inclinometer
3 weeks
Study Arms (2)
iPhone measurement application
EXPERIMENTALFor the measurement, the participant was asked to lie on his side and flex the knee to 90 degrees. The examiner stabilized the patient from the pelvis with one hand, and with the other hand brought the flexed leg of the participant to abduction and extension. The Examiner 3 recorded the result by placing the device to be measured on the lateral projection of the midpoint of the femur.
Bubble inclinometer
ACTIVE COMPARATORmeasurement will be done by the same method. For the measurement, the participant was asked to lie on his side and flex the knee to 90 degrees. The examiner stabilized the patient from the pelvis with one hand, and with the other hand brought the flexed leg of the participant to abduction and extension. The Examiner 3 recorded the result by placing the device to be measured on the lateral projection of the midpoint of the femur.
Interventions
The iPhone measurement application will be used to ensure validity and reliability.
Bubble inclinometer with proven validity and reliability will be used for this study.
Eligibility Criteria
You may qualify if:
- Being between the ages of 20 and 45 and agreed to participate the study.
You may not qualify if:
- Having hip or knee surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
KTO Karatay University
Konya, 42020, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- The Examiner 3 will be record the result by placing the device to be measured on the lateral projection of the midpoint of the femur. By preserving the participant's position, measurements will be make with the other device immediately and the values will bw record by the Examiner3.
- Purpose
- DIAGNOSTIC
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 4, 2021
First Posted
March 9, 2021
Study Start
March 8, 2021
Primary Completion
April 24, 2021
Study Completion
April 26, 2021
Last Updated
September 8, 2021
Record last verified: 2021-03
Data Sharing
- IPD Sharing
- Will not share