NCT04787900

Brief Summary

The validity and reliability of adduction angle measurement of hip with smartphone will be investigate.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
4 days until next milestone

Study Start

First participant enrolled

March 8, 2021

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 9, 2021

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 24, 2021

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 26, 2021

Completed
Last Updated

September 8, 2021

Status Verified

March 1, 2021

Enrollment Period

2 months

First QC Date

March 4, 2021

Last Update Submit

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

EXPERIMENTAL

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.

Device: iPhone measurement application

Bubble inclinometer

ACTIVE COMPARATOR

measurement 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.

Device: Bubble inclinometer

Interventions

The iPhone measurement application will be used to ensure validity and reliability.

iPhone measurement application

Bubble inclinometer with proven validity and reliability will be used for this study.

Bubble inclinometer

Eligibility Criteria

Age20 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

MeSH Terms

Conditions

Iliotibial Band Syndrome

Condition Hierarchy (Ancestors)

Knee InjuriesLeg InjuriesWounds and InjuriesCumulative Trauma DisordersSprains and Strains

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
Model Details: wo 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.
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

Locations