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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05579613
Other study ID # P.T.REC/012/003549
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 20, 2022
Est. completion date October 3, 2022

Study information

Verified date October 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Forward head posture (FHP) is one of the most common postural deformities, which affects 66% of the patient population and this study will be designed to investigate the effect of interactive virtual reality device on cervical proprioception and range of motion in symptomatic forward head posture.


Description:

Thirty subjects of both sex with ages ranging from 20-24 years and BMI ranging from 18-25 kg/m² with symptomatic forward head posture will be participated in this study. They will be assigned randomly to two groups. Group A will receive traditional treatment (chin tuck exercise for posture correction); 3 min each day for 4 weeks, three sets of 10 repetitions (each repetition was held for 5 sec) were performed. Group B will receive the same as group "A" and received VR training by Xbox Kinect 360 (15 min per session 3 times per week) for 4 weeks. Cervical joint position error (JPE) (CROM device) and cervical range of motion will be measured pre and post treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date October 3, 2022
Est. primary completion date July 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria : 1. Subject's age range from 18-24 years old distance of = 2 cm between the acromion and the earlobe when they were positioned perpendicular to the ground.( Kim et al 2018). 2. Prolonged neck pain for more than three months; and the Neck Disability Exclusion Criteria:1- Existing vestibular pathology. 2- Cervical fracture/dislocation. 3- Sys- temic diseases. 4- Neurological/cardiovascular/respiratory disorders affecting physical performance. 5- History of traumatic head injury. 6- Pregnancy. -

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Interactive virtual reality device
The Kinect sensor is an infrared camera that can recognize the positions and motions of the player without the need for special controller. The console controls the various games .For the VR training, the Xbox Kinect, console, and monitor will set up in a dedicated space. The patient will placed 1.5-2 m away from the Kinect sensor.

Locations

Country Name City State
Egypt Ibtsam Abdelkarim Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cervical propriception Assessment of cervical proprioception using cervical range of motion 4 weeks
Primary Cervical range of motion Assessment of cervical range of motion by CROM 4 weeks
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