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Clinical Trials/NCT05392049
NCT05392049
Unknown
Not Applicable

Comparative Effects of Bowen's and Post Isometric Relaxation Techniques on Pain, Range of Motion and Function in Patients With Temporomandibular Joint Disorder

Riphah International University1 site in 1 country24 target enrollmentStarted: June 1, 2022Last updated:

Overview

Phase
Not Applicable
Enrollment
24
Locations
1
Primary Endpoint
NPRS for pain

Overview

Brief Summary

the aim of this study to compare effects of Bowen's therapy and post isometric relaxation techniques on pain, range of motions and function in patients with TMJ disorder.

Detailed Description

Temporomandibular joint disorder is a very common and serious problem of mouth and face pain related condition that mostly effect in quality of life and compromise the daily functional activities of a patient. It can be caused by any trauma, biomechanical, neuromuscular and psychologically related problems. Patient may come in acute and chronic phase. Patient condition mostly vary and worsen day by day, it thoughts that TMJD going interval throw out the life span of patient. Medicine, physical therapy interventions and surgical procedures are use in treatment of TMJ disorder. This study will conducted the comparative effects of Bowen's and post-isometric relaxation techniques on pain, ROM and functions in TMJ patients.

The study would be randomized clinical trial. Total 24 subjects will be assigned randomly into two groups by using lottery methods. Baseline treatment will be same (ultrasound, tapping) in both groups. Group A will be treated by Bowen's therapy and Group B will be treated by post-isometric relaxation technique for 30 min session (2 sessions/week and total 4 weeks). Numeric Pain Rating Scale, maximum mouth opening inter-incisal rural and jaw functional limitation scale-20 would be used as an outcome measurement tool for pain, range of motion and function respectively. Measurement will be taken at Baseline and at the end of the 4th week's treatment session. After assessing the normality data will be analyzed by using parametric / nonparametric test.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male and Female Participant aged 20-
  • Pain on function.
  • Restricted jaw movement.
  • Clicking, popping sound.
  • Tenderness in muscle of mastication.
  • Joint tenderness.
  • With a restricted mandibular range of motion 40mmor less measured interincisal.

Exclusion Criteria

  • Systematic arthropathy such as.
  • Rheumatoid arthritis
  • Fracture of jaw or TMJ.
  • Malignant history of face and jaw.
  • Prevent history of jaw or TMJ surgery.
  • Subject has/ had dental/ orthodontic treatment within the past 14 days

Outcomes

Primary Outcomes

NPRS for pain

Time Frame: 4th week

The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).

Jaw Functional Limitation Scale for functional activity

Time Frame: 4th week

Jaw functional limitation is a 20 items,3 level functional scale mastication, vertical jaw mobility, emotional and verbal expression. NO LIMITATION'' score have 0 and SEVER LIMITATION '' have 10 score

Maximum Mouth opening (Inter- incisal Rural) for rang of motion

Time Frame: 4th week

Maximum mouth opening is a vital and objective clinical parameter for assessment of stomatognathic region and it represents the range of vertical mandibular range of movement.The distance between the upper central incisor and lower incisor determined by flexible intra-oral ruler ,it is valid and reliable tool for measure TMJ distance.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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