The Effectiveness of Temporomandibular Joint Mobilization and Exercise in Individuals With Chronic Neck Pain

Sponsor
Uskudar University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06005922
Collaborator
(none)
50
1
2
2
24.9

Study Details

Study Description

Brief Summary

To examine the effects of temporomandibular joint mobilization and exercises added to the conventional physiotherapy program on posture, functionality and muscular endurance in individuals with chronic neck pain.

Condition or Disease Intervention/Treatment Phase
  • Other: physiotherapy
  • Other: TMJ exercises
N/A

Detailed Description

Our research is a randomized controlled trial. 50 participants will be included in the study, which will be conducted on individuals aged 18-65 years with chronic neck pain. Participants will be divided into 2 groups as experimental and control groups by simple randomization method. All patients will be treated with conventional physiotherapy methods for 4 weeks and 5 days a week. In addition to conventional treatment, temporomandibular joint mobilization techniques were applied to the experimental group; exercises will be given. In the study, temporomandibular dysfunction (TMD) Pain Screener, Neck Disability Index, and Visual Analog Scale questionnaires will be applied to the patients twice, before and after the treatment. Before and after the treatment, the cervical region's range of motion and muscular endurance will be measured by the physiotherapist. Pre- and post-intervention data were statistically analyzed and compared.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
temporomandibular joint mobilization and temporomandibular joint exercisestemporomandibular joint mobilization and temporomandibular joint exercises
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Investigation of the Effectiveness of Temporomandibular Joint Mobilization and Exercise on Posture, Endurance and Functionality in Individuals With Chronic Neck Pain
Anticipated Study Start Date :
Sep 15, 2023
Anticipated Primary Completion Date :
Oct 20, 2023
Anticipated Study Completion Date :
Nov 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: conventional physiotherapy methods

conventional physiotherapy methods

Other: physiotherapy
ultrasound hotpack electrotherapy joint range of motion exercises isometric neck exercises stretching exercises

Experimental: temporomandibular joint (TMJ) group

conventional physiotherapy methods and temporomandibular joint mobilization and temporomandibular joint exercises

Other: physiotherapy
ultrasound hotpack electrotherapy joint range of motion exercises isometric neck exercises stretching exercises

Other: TMJ exercises
tongue relaxation position TMJ isometric strengthening exercises Posture exercises Isometric neck extension in neutral position back extension Strengthening the abdominal muscles Supine dorsal stretch pectoral stretch

Outcome Measures

Primary Outcome Measures

  1. Neck Disability Index [6 weeks]

    The survey consists of 10 questions. Each question has 5 options. For each question, points are given as A:0, B:1, C:2 D:3 E:4, F:4. 0-4 points are defined as no disability, 5-14 points as mild disability, 15-24 points as moderate disability, 25-34 points as severe disability, 35 or above points as complete disability.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being between the ages of 18-65,

  • Having neck pain lasting longer than 3 months,

  • Absence of known systemic disease or trauma history,

  • Volunteering to participate in the research.

Exclusion Criteria:
  • Having a history of trauma in the areas that are the subject of the study, such as head and neck surgery, upper extremity, thoracic and cervical vertebrae,

  • Disc displacement, osteoarthrosis, osteoarthritis signs and symptoms

  • Having a neurological-psychiatric diagnosis that may affect the measurement results.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medicana Hospital Umraniye İstanbul Turkey

Sponsors and Collaborators

  • Uskudar University

Investigators

  • Study Chair: Şeyma DELCEOĞLU, Uskudar University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Öğr. Üyesi Ömer Şevgin, Asst. Prof. Dr., Uskudar University
ClinicalTrials.gov Identifier:
NCT06005922
Other Study ID Numbers:
  • Uskudar63
First Posted:
Aug 23, 2023
Last Update Posted:
Aug 24, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Öğr. Üyesi Ömer Şevgin, Asst. Prof. Dr., Uskudar University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2023