Validity and Reliability of Rebee Sensor to Measure Knee ROM

NCT05137951 | Completed

• 1 other identifier: Validity of rebee sensor (PT)
• Study Type: observational
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

This study was conducted to investigate: The criterion related validity of Rebee wearable sensor in measuring active flexion and extension of knee joint ROM compared with digital goniometer measurement. The intra-rater reliability of Rebee wearable sensor in measuring active flexion and extension of knee joint ROM compared with digital goniometer measurement.

Conditions

Physical Therapy Modalities

Keywords

Rebee Sensor; Digital goniometer; Knee joint Range of motion

Outcome Measures

Primary Outcomes (2)

• test Validation of rebee wearable sensor for measuring knee Range of motion

  The criterion related validity andof Rebee wearable sensor in measuring active flexion and extension of knee joint ROM compared with digital goniometer measurement.

  day 1

• test intrarater reliability of rebee wearable sensor to measure active knee flexion and extension ROM

  the procedures was repeated two times with one week interval between measurements. Researcher was recorded all the measurement.

  day 1

Interventions

Rebee sensor DEVICE

Rebee is a wearable motion sensor package of sensor with its own mobile application, which measures range of joint movement in different planes easily which the patient able to wear the sensor and move easily to measure ROM and record the measurement at the application software Digital goniometer Goniometry has been described as a tool to measure angle. It gives the physician a useful method to diagnose musculoskeletal function in terms of ROM, monitor the progress of an intervention, record the data for future follow-up, and meet statutory and legal requirements for impairment rating and disability determinations where applicable

Also known as: Digital goniometer

Eligibility Criteria

• Age: 30 Years - 45 Years
• Sex: all
• Age Groups: Adult (18-64)
• Sampling Method: Probability Sample

Study Population

The participants were recruited from Faculty, staff, and students of Pharos University, Alexandria, Egypt. Graduate Program in Physical Therapy after achieving the inclusion criteria .

You may qualify if:

• Forty normal participant's age ranged from 30 to 45.
• The participant from both sex.
• Participant Body mass index (BMI) from (19 to 25) normal weight (BMI= weight (kg) / \[height (m)\] 2)

Sponsors & Collaborators

• Cairo University: lead

Study Sites (1)

Pharos university at alexandria

Alexandria, 21500, Egypt

Location

Study Officials

• Wadida H Abd elkader, PhD

  Professor.dr

  STUDY DIRECTOR

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: demonstrator of basic science faculty of physical therapy

Study Record Dates

• First Submitted: October 3, 2021
• First Posted: November 30, 2021
• Study Start: June 1, 2021
• Primary Completion: September 1, 2021
• Study Completion: September 25, 2021
• Last Updated: December 13, 2021

Record last verified: 2021-11

Locations

EG (1)