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Effect of Virtual Reality on TMD Following Maxillofacial Surgery

Cairo University (CU) logo

Cairo University (CU)

Status

Active, not recruiting

Conditions

Temporomandibular Disorder

Treatments

Other: Virtual reality
Other: Traditional exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT06537661
P.T.REC/012/005153

Details and patient eligibility

About

Sixty eight patients who have TMJ pain and ROM restriction after maxillofacial surgery participated in this study , they are selected from government hospitals (general and insurance ).

Will be randomly divided into two equal groups ( group A, group B ). Their ages range from 20 - 35 years.

The Purpose of the study is to evaluate the therapeutic efficacy of VR in decreasing pain and improve ROM for Patients after maxillofacial surgery.

Full description

Sixty eight patients who have TMJ pain and ROM restriction after maxillofacial surgery participated in this study , they are selected from government hospitals (general and insurance ).

Will be randomly divided into two equal groups ( group A, group B ). Their ages range from 20 - 35 years.

The VR glasses which were the source of visual and auditory feedback, were connected by Bluetooth to a mobile phone and all the videos of selected tasks (tasks of Active mobility exercises and isometric contraction exercises, massage exercises) were turned on. Active mobility exercises (jaw opening 6 times of 30 s; lateralization 10 times of 5 s; protrusion 10 times Of 5 s).

  • Self-massage masticatory Muscles, After each session.
  • Isometric contraction exercises The Purpose of the study is to evaluate the therapeutic efficacy of VR in decreasing pain and improve ROM for Patients after maxillofacial surgery.

Enrollment

2 estimated patients

Sex

All

Ages

30 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • The subject selection will be according to the following criteria:

    • Patients after Arthrocentesis .
    • Patients after Temporomandibular joint condylar discopexy.
    • Age ranges between 30 - 45 years.
    • All patients will have informed consent .Exclusion Criteria:
  • • Surgery That conducted on the temporomandibular joint (meniscectomy, arthroscopy, etc.).

    • oral surgery (e.g., surgery for impaction of the third molar), as well as patients with concomitant systemic or neurological conditions.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

2 participants in 2 patient groups

Study group
Experimental group
Description:
VR and traditional Ex
Treatment:
Other: Virtual reality
Control group
Experimental group
Description:
traditional physical therapy ex
Treatment:
Other: Traditional exercises

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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