Ignite Creation Date:
2024-05-06 @ 3:51 PM
Last Modification Date:
2024-10-26 @ 1:58 PM
Study NCT ID:
NCT04787900
Status:
COMPLETED
Last Update Posted:
2021-09-08
First Post:
2021-03-04
Brief Title:
Reliability and Validity of iPhone Application for OBER
Sponsor:
KTO Karatay University
Organization:
KTO Karatay University
Study Overview
Official Title:
Concurrent Validity and Reliability of the iPhone Measurement Application to Evaluate Iliotibial Band Length
Status:
COMPLETED
Status Verified Date:
2021-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The validity and reliability of adduction angle measurement of hip with smartphone will be investigate
Detailed Description:
Our study is to investigate the intra-rater reliability inter-rater reliability and concurrent validity of iPhone Measurement Applications to measure iliotibial band length in individuals without iliotibial band-related pathology The aim of this study is to evaluate the intra-rater reliability inter-rater reliability and concurrent validity of bubble inclinometer and iPhone Measurement Applications in the evaluation of iliotibial band tension in healthy individuals This research is being done to determine if there are other more reliable valid or innovative technological ways to measure iliotibial band length
Participants
A priori power analysis indicated that a minimum 16 or more participants should be enrolled the study for a correlation of 07 with an α level of 05 and power of 95 The study protocol comply with the Declaration of Helsinki for Human Experimentation Participants were excluded if they had hip or knee surgery in the past year and iliotibial band syndrome All participants provide written informed consent Permission for the study was obtained from KTO Karatay University Faculty of Medicine Drug and Non-Medical Device Research Ethics Committee with decision number 2019012
Two experienced physiotherapists will evaluate the elasticity of both the dominant and non-dominant iliotibial bands after 2 minutes of warm-up before the evaluation Measurements will be made by two physical therapists for each participant in different rooms without seeing each other The examiners will carry out three measurements for both extremities using both the bubble inclinometer and the iPhone measurement app A 5-minute passive rest will be give between measurements All evaluations will be first conducted by Examiner 1 and then by Examiner 2 Measurement values will be record by a third physiotherapist Data obtained from both devices will be compare in terms of validity and reliability using statistical analysis used in previous studies
All inclinometric measurements will be do by two independent blind examiners BSU and HG and the range of motion ROM will be read directly from the devices by a third examiner
Before the first measurement the participant will be ask to warm up for five minutes For the measurement the participant will be ask to lie on his side and flex the knee to 90 degrees The examiner will stabilize 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 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 participants position measurements will be make with the other device immediately and the values will bw record by the Examiner3
After the first measurement second and third measurements will be take at 2-minute passive intervals
After the participants will complete their first examiner evaluation they will move to the second examiners room The same protocol will be use for all measurements by the Examiner 2
Instruments We will use 2 devices to measure iliotibial band length bubble inclinometer Baseline Fabrication Enterprises Inc New York and iPhone Measurement Applications Apple Inc California The iPhone Measurement Applications measurements will make with the iPhone 6s plus running IOS 1331 Apple Inc California
Participants
A priori power analysis indicated that a minimum 16 or more participants should be enrolled the study for a correlation of 07 with an α level of 05 and power of 95 The study protocol comply with the Declaration of Helsinki for Human Experimentation Participants were excluded if they had hip or knee surgery in the past year and iliotibial band syndrome All participants provide written informed consent Permission for the study was obtained from KTO Karatay University Faculty of Medicine Drug and Non-Medical Device Research Ethics Committee with decision number 2019012
Two experienced physiotherapists will evaluate the elasticity of both the dominant and non-dominant iliotibial bands after 2 minutes of warm-up before the evaluation Measurements will be made by two physical therapists for each participant in different rooms without seeing each other The examiners will carry out three measurements for both extremities using both the bubble inclinometer and the iPhone measurement app A 5-minute passive rest will be give between measurements All evaluations will be first conducted by Examiner 1 and then by Examiner 2 Measurement values will be record by a third physiotherapist Data obtained from both devices will be compare in terms of validity and reliability using statistical analysis used in previous studies
All inclinometric measurements will be do by two independent blind examiners BSU and HG and the range of motion ROM will be read directly from the devices by a third examiner
Before the first measurement the participant will be ask to warm up for five minutes For the measurement the participant will be ask to lie on his side and flex the knee to 90 degrees The examiner will stabilize 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 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 participants position measurements will be make with the other device immediately and the values will bw record by the Examiner3
After the first measurement second and third measurements will be take at 2-minute passive intervals
After the participants will complete their first examiner evaluation they will move to the second examiners room The same protocol will be use for all measurements by the Examiner 2
Instruments We will use 2 devices to measure iliotibial band length bubble inclinometer Baseline Fabrication Enterprises Inc New York and iPhone Measurement Applications Apple Inc California The iPhone Measurement Applications measurements will make with the iPhone 6s plus running IOS 1331 Apple Inc California
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None