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Art-Based Pain Assessment Tool in Patients With Temporomandibular Joint Disorders

K

King Abdulaziz University

Status and phase

Enrolling
Phase 3

Conditions

Temporomandibular Disorders (TMD)
Wilkes 1 and 2
TMD Art Pain Study
Art Therapy
TMJ - Oral &Amp;Maxillofacial Surgery
TMJ Pain

Treatments

Diagnostic Test: Artistic Pain Exploration (APE) Method
Diagnostic Test: Standard TMD Assessment

Study type

Interventional

Funder types

Other

Identifiers

NCT07018791
02-01-25

Details and patient eligibility

About

Title of Study:

Assessment of the Impact of Art-Based Pain Assessment Tool on Pain Communication, Joint Function, and Anxiety in Patients with Temporomandibular Disorders (TMD): A Randomized Controlled Trial

Location:

King Abdulaziz University Dental Hospital (KAUFD), Jeddah, Saudi Arabia What Is This Study About?

This study examines how an art-based tool can help improve communication and understanding of pain among patients with jaw joint disorders (TMD). It compares two groups:

  • Standard care: Routine diagnostic and therapeutic procedures
  • Intervention: Standard care plus a guided art-based tool using paintings to express and discuss the TMD experiences What Is the Art-Based Tool?

This novel method, called the Artistic Pain Exploration (APE), uses paintings to help patients describe their pain that relates to TMD and its effect on their quality of life:

  1. Participants will be shown three paintings (e.g., The Scream by Edvard Munch)
  2. Participants will choose the one that best resonates with them
  3. A guided discussion follows, exploring how the image relates to their physical and emotional pain as well as the effect of pain on their daily activities

Research Questions:

  1. Does using the APE method help participants better communicate and understand their pain?
  2. Does it improve jaw function and reduce anxiety more than standard assessment? Who Can Participate?

Participants may be eligible if they:

  • Are 18 years or older
  • Have early-stage TMD (not needing surgery)
  • Can give informed consent

Participants cannot participate if they:

  • Require jaw surgery
  • Have severe mental illness (e.g., psychosis or bipolar disorder)
  • Take narcotic pain medications regularly What Will Happen During the Study?
  • Participants are randomly assigned to one of the two groups.
  • Each participant will complete a standardized questionnaire before and after two weeks to assess the level of anxiety.
  • All participants will be screened for depression via a standardized questionnaire before the first visit.
  • All will undergo a clinical exam to assess the TMJ pain and function and receive appropriate medications and lifestyle instructions.
  • Some participants (intervention group) will also discuss their pain using the artwork.
  • All participants will be seen for a follow up in 2 weeks to assess the TMJ function and pain.

Potential Risks and Discomforts

Participants may experience:

  • Emotional discomfort while discussing pain
  • Mild anxiety during interviews or questionnaires If needed, a psychiatrist on the research team will provide support or referrals.

Potential Benefits

  • A better understanding of pain
  • Improved communication with care provider
  • Possible improvement in pain and jaw function

Costs There are no costs to participate. All treatments are provided free of charge.

Compensation / Treatment for Injury

  • If participants experience harm from this study, necessary medical care will be provided by the research team.
  • No financial compensation will be provided by King Abdulaziz University.

Confidentiality Participants' identity and medical records will remain confidential. Only approved researchers and auditors will have access to data, in accordance with applicable laws. Any results published will not include participants' name or identifying details.

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults aged 18 years or older
  • Diagnosed with Temporomandibular Disorders (TMD) requiring conservative management only and classified as Wilkes' stage I or II
  • Able to understand and sign the informed consent form

Exclusion criteria

  • Patients requiring surgical intervention for TMD
  • Presence of severe mental illness, such as psychotic disorders or bipolar affective disorders
  • Regular use of narcotic (opioid) pain medications

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

Control Group
Active Comparator group
Description:
Participants in this group receive standard care for Temporomandibular Joint Disorders (TMD), which includes a clinical examination, assessment of pain using the Visual Analogue Scale (VAS), anxiety and depression screening (GAD-7 and PHQ-9), evaluation of jaw pain and function, and conservative treatment through medication and self-care instructions.
Treatment:
Diagnostic Test: Standard TMD Assessment
Intervention Group
Experimental group
Description:
Participants in this group receive the same standard care as the control group, with the addition of an art-based method designed to enhance the understanding and communication of pain.
Treatment:
Diagnostic Test: Standard TMD Assessment
Diagnostic Test: Artistic Pain Exploration (APE) Method

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Razan M Baabdullah, BDS, MS, FRCDC

Data sourced from clinicaltrials.gov

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