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Active, not recruitingNCT06537661Updated Aug 5, 2024

Effect of Virtual Reality on TMD Following Maxillofacial Surgery

An interventional study of Virtual reality and Traditional exercises in Temporomandibular Disorder, sponsored by Cairo University. Active, not recruiting at 2 sites in Egypt. Open to participants aged 30 Years to 45 Years. Per ClinicalTrials.gov, last updated 2024-08-05.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Mar 2024, registered Jul 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
2
Allocation
Randomized
Ages
30 Years to 45 Years
Sex
All
01

Study summary

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.

Read the detailed 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.
02

Conditions studied

  • Temporomandibular Disorder

Keywords

  • VR
  • TMD
  • Maxillofacial surgery
03

In context

Temporomandibular Joint Disorders

609 studies on the registry are indexed under Temporomandibular Joint Disorders; 160 are open to participants now.

This study's planned enrollment of 2 is below the median of 46 across 434 interventional studies indexed under Temporomandibular Joint Disorders.

Browse Temporomandibular Joint Disorders studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility 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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
2 participants (estimated)

Study arms

  • Experimental
    Study group

    VR and traditional Ex

    Other: Virtual reality

  • Experimental
    Control group

    traditional physical therapy ex

    Other: Traditional exercises

Interventions

  • OtherVirtual reality

    Virtual reality (VR): is the artificial construction of a 3D environment viaThe 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.

  • OtherTraditional exercises

    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 Were included (3 times of 10 s)

06

What researchers measure

Primary outcomes

  1. Measure pain

    Measure by visual analog scale (VAS) 0: low in pain 10:high in pain

    Time frame: 6weeks

Secondary outcomes

  1. Maximum mouth opnening (MMO )

    Measure by milemeter

    Time frame: 6weeks

07

Study locations

2 sites
  • Nehal mohamed
    Giza, 20, Egypt
  • Nehal mohamed
    Giza, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06537661
Lead sponsor
Cairo University
Responsible party
Nehal mohamed soliman Elbkery (Principal investigator, Cairo University) — Principal investigator
First posted
Aug 5, 2024
Start date
Mar 10, 2024
Primary completion
Jul 1, 2024
Completion
Sep 10, 2024 (estimated)
Last update
Aug 5, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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