NCT06537830

Brief Summary

Objective: The aim of this study is to examine the validity and reliability of a wearable motion sensor, which is an inertial measurement units (IMUs) sensor, in measuring knee joint active flexion movement angles. Methods: The study included 70 Health Sciences Faculty students between the ages of 18-25. The dominant knee joint range of motion of the participants was measured by two raters with a digital goniometer (Meloq EasyAngle) and wearable motion sensors (MetaMotionRL). A 10-minute rest was given between each measurement. The data were analyzed using the IBM® SPSS® Statistics for Windows software (Version 27.0). Mean ± standard deviation (Mean ± SD) and percentage (%) were used for the descriptive variables. Intra- and inter-rater reliability was tested with intraclass correlation coefficient (ICC) and Bland-Altman analysis. ICC values less than 0.5 were classified as poor, values between 0.5 and 0.75 as moderate, values between 0.75 and 0.9 as good, and values greater than 0.90 as excellent reliability. Paired samples t test was used to compare test-retest measurements. Concurrent validity was determined by Pearson correlation coefficient. The significance value was accepted as p\<0.05.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
70

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2021

Shorter than P25 for all trials

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

Study Start

First participant enrolled

December 15, 2021

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2022

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2022

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

July 28, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

August 5, 2024

Completed
Last Updated

August 5, 2024

Status Verified

August 1, 2024

Enrollment Period

5 months

First QC Date

July 28, 2024

Last Update Submit

August 1, 2024

Conditions

Keywords

Wearable motion sensorsMetamotionRLIMUs

Outcome Measures

Primary Outcomes (2)

  • Digital goniometer measurement

    Participants were asked to wear shorts that exposed their knees. While the participants were lying in the prone position on the examination table, their dominant knee range of motion was measured with EasyAngle (Meloq©, Stockholm, Sweden) digital goniometer by physiotherapists (rater I). The participant was instructed to bend his knee and bring his heel as close to his hip as possible. The degree of dominant knee active flexion was measured three times by the rater I with a EasyAngle (Meloq©, Stockholm, Sweden) digital goniometer (the pivot point was determined as the lateral epicondyle of the femur), and the highest value was recorded.

    at baseline

  • MetaMotionRLs measurement

    Two MetaMotionRLs were fixed to the lateral thigh and leg with velcro strap, at the level of the midpoint of the tibia and femur in the dominant lower extremity by the rater I. Two MetaMotionRL motion sensors were used simultaneously. MetaMotionRL was used by connecting via Bluetooth with the free MetaROM (application) smart phone application. The participant was asked to flex his knee as much as possible. Three measurements were made and the highest value shown in the app was recorded. Following this, the sensors were removed and placed again after 10 minutes and measured a second time by the same rater using the same method, the highest value was recorded. Following removal of the sensors, the participant was taken to a different examination table in the same room. And the rater II placed the sensors and repeated the MetaMotionRL measurement.

    at baseline

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Seventy healthy student were included between December 2021 and April 2022, the study was approved by Haliç University Non-Invasive Ethics Committee (173/01.12.2021). All participants completed written informed consent. Seventy healthy students (40 female, 30 male) from Haliç University Faculty of Health Sciences were included in the study.

You may qualify if:

  • being between the ages of 18-25
  • volunteering to participate in the study

You may not qualify if:

  • a history of orthopedic surgery or trauma to the lower extremity
  • knee pain felt during joint range of motion measurement
  • inability to maintain a prone position

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Halic University

Istanbul, 34445, Turkey (Türkiye)

Location

Study Officials

  • Melek Güneş Yavuzer, Prof.

    Halic University

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 28, 2024

First Posted

August 5, 2024

Study Start

December 15, 2021

Primary Completion

April 30, 2022

Study Completion

July 15, 2022

Last Updated

August 5, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations