ClinicalTrials.Veeva

Menu

Effects of a Biopsychosocial Approach Added to Physiotherapy in Temporomandibular Disorders (TMD-BPS)

B

Betül Özata

Status

Not yet enrolling

Conditions

Temporomandibular Disorders (TMD)

Treatments

Other: Physiotherapy Program
Other: Biopsychosocial Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT07320144
2025310 (Other Grant/Funding Number)
TMD-BPS-2025

Details and patient eligibility

About

Temporomandibular disorders are conditions that affect the jaw joint and surrounding muscles and may cause pain, limited jaw movement, stress, sleep problems, and teeth grinding. Physiotherapy is commonly used to manage these problems, but psychological and social factors may also influence symptoms.

The purpose of this study is to examine whether adding a biopsychosocial approach to physiotherapy improves stress levels, sleep quality, and bruxism in individuals with temporomandibular disorders. Participants will receive either physiotherapy alone or physiotherapy combined with education about pain, stress management, and sleep habits. The results of this study may help improve treatment strategies for people with temporomandibular disorders.

Full description

This randomized interventional study aims to investigate the effects of adding a biopsychosocial approach to physiotherapy in individuals with temporomandibular disorders. Temporomandibular disorders are multifactorial conditions influenced by physical, psychological, and social factors. While physiotherapy is effective in reducing pain and improving function, psychosocial factors such as stress, sleep disturbance, and bruxism may contribute to symptom persistence.

Participants will be randomly assigned to one of two groups. The control group will receive a standardized physiotherapy program including therapeutic exercises and manual therapy targeting the temporomandibular joint and related musculoskeletal structures. The intervention group will receive the same physiotherapy program in addition to a biopsychosocial intervention consisting of pain neuroscience education, stress management strategies, and sleep hygiene education.

Outcome measures will include stress levels, sleep disturbance, and bruxism severity as primary outcomes, and pain intensity and jaw function as secondary outcomes. Assessments will be conducted at baseline and after the intervention period. This study is expected to provide evidence on the effectiveness of integrating a biopsychosocial approach into physiotherapy for temporomandibular disorders.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with temporomandibular disorders
  • Age between 18 and 65 years
  • Presence of stress, sleep disturbance, or bruxism symptoms
  • Ability to understand and follow study instructions
  • Willingness to participate and provide informed consent

Exclusion criteria

  • History of temporomandibular joint surgery
  • Presence of neurological, rheumatological, or systemic diseases affecting the musculoskeletal system
  • Current orthodontic treatment
  • Use of medications that may affect pain perception or sleep
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Physiotherapy
Active Comparator group
Description:
Participants in this arm will receive a standardized physiotherapy program for temporomandibular disorders, including therapeutic exercises and manual therapy targeting the temporomandibular joint and associated musculoskeletal structures.
Treatment:
Other: Physiotherapy Program
Physiotherapy Plus Biopsychosocial Approach
Experimental group
Description:
Participants in this arm will receive the same physiotherapy program combined with a biopsychosocial intervention including pain education, stress management strategies, and sleep hygiene education.
Treatment:
Other: Biopsychosocial Intervention
Other: Physiotherapy Program

Trial contacts and locations

0

Loading...

Central trial contact

Betül Özata, MSc

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems