KinectROM Application for Assessing Range of Motion in Upper and Lower Extremity: A Development and Validation Study

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03731507

Acronym

KinectROM

Enrollment

Registered

2018-11-06

Start date

2018-11-05

Completion date

2018-12-15

Last updated

2020-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Range of Motion

Keywords

range of motion, upper extremity, lower extremity

Brief summary

The aim of the study is to investigate the validity and reliability of KinectROM application for objectively evaluating range of motion (ROM)

Detailed description

The application KinectROM called has been developed for assessing ROM with Kinect controller by our team. So, shoulder, elbow, knee, hip and ankle ROM measurements will be made with universal goniometer and developed KinectROM application.

Interventions

DEVICEAssessment of Range of Motion with Kinect Controller

A ROM measurement method called as KinectROM by us has been developed with Kinect Controller

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 40 Years

Healthy volunteers

Yes

Inclusion criteria

-Healthy individuals with 18-40 years

Exclusion criteria

-Have any limited extremity between the ages of 18-40 years.

Design outcomes

Primary

Measure	Time frame	Description
Range of Motion	baseline	ROM of shoulder, elbow, knee, hip and ankle will be made with universal goniometer and developed Kinect controller based measurement method.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026