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Comparison of the Effects of Two Types of Exercise on Women with Upper Crossed Syndrome and Temporomandibular Joint Disorder

Comparing the Effects of McKenzie Exercises and PNF on Angles, Performance, and Symptoms in Women with Upper Crossed Syndrome and Temporomandibular Joint Disorder: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250504065596N1
Enrollment
42
Registered
2025-08-27
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Temporomandibular Joint Disorder. Condition 2: Upper Cross Syndrom. Temporomandibular joint disorders

Interventions

Intervention 1: Control group: No intervention is applied. Only assessment of Upper Crossed Syndrome and Temporomandibular Joint Disorder (TMD) is performed initially, and then reassessed six months l

Sponsors

Shahid Beheshti University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Voluntary Participation Body Mass Index between 18 and 25 Diagnosis of TMD based on the specialist's assessment At least one month has passed since the onset of TMD pain "Forward head posture = 50 degrees, forward shoulder posture = 52 degrees, and hyper kyphosis = 40 degrees." Female participants only 20 to 40 years old Presence of clicking sounds in the temporomandibular joint(TMJ) Functional disability of the temporomandibular joint (TMJ) Presence of pain in the temporomandibular joint (TMJ) and associated structures

Exclusion criteria

Exclusion criteria: Use of medication or other interventions Presence of specific spinal pathologies such as severe disc herniation (grade II or III) History of spinal fracture or surgery Presence of severe deformities in the lumbar spine or pelvis Presence of rheumatologic disorders Presence of sequestrated (migrated) disc displacement, TMJ osteoarthritis, or arthritis according to DC/TMD criteria History of traumatic injuries to the mandible or cervical spine Presence of fibromyalgia syndrome Presence of systemic diseases (rheumatoid arthritis, systemic lupus erythematosus, or psoriatic arthritis) Presence of neurological disorders History of any treatment (physiotherapy, splint therapy, or acupuncture) within 3 months prior to the study

Design outcomes

Primary

MeasureTime frame
Forward Head. Timepoint: One day before the start of the study, followed by six weeks of training, and then one day after the end of the training. Method of measurement: Photogrammetry method for evaluating upper crossed syndrome.;Shoulder Forward. Timepoint: One day before the start of the study, followed by six weeks of training, and then one day after the end of the training. Method of measurement: Photogrammetry method for evaluating upper crossed syndrome.;Kyphosis. Timepoint: One day before the start of the study, followed by six weeks of training, and then one day after the end of the training. Method of measurement: Photogrammetry method for evaluating upper crossed syndrome.;Temporomandibular joint noise. Timepoint: One day before the start of the study, followed by six weeks of training, and then one day after the end of the training. Method of measurement: Diagnostic Criteria for Temporomandibular Disorders.;Temporomandibular joint pain. Timepoint: One day before the start of the study, followed by six weeks of training, and then one day after the end of the training. Method of measurement: Diagnostic Criteria for Temporomandibular Disorders.;Temporomandibular joint function. Timepoint: One day before the start of the study, followed by six weeks of training, and then one day after the end of the training. Method of measurement: Diagnostic Criteria for Temporomandibular Disorders.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSarvenaz Shabani Panbecholeh

Shahid Beheshti University

sarvenazshabani@yahoo.com+98 21 6659 5554

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026