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NCT Number: NCT06537661

Effect of Virtual Reality on TMD Following Maxillofacial Surgery

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

30 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nehal mohamed, Giza, Egypt

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Virtual Reality

Other

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.

Traditional exercises

Other

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)

Primary outcomes

  1. Measure pain

    Time frame: 6weeks

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

Secondary outcomes

  1. Maximum mouth opnening (MMO )

    Time frame: 6weeks

    Measure by milemeter

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

VIRTUAL REALITY and TEMPOROMANDIBULAR DISORDER FOLLOWING MAXILLOFACIAL SURGERY

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Aug 5, 2024
Registry last updated
Aug 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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