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Completed

NCT Number: NCT05966103

Efficacy of Scapulothoracic Exercises on Postural Stability, Proprioception, Muscular Features and Mandibular Functions

The goal of this Randomized, Double-Blind, Clinical Trial is to investigate the effects of scapulothoracic exercises on postural stability, muscle strength, muscular endurance, mandibular functions and proprioception in sedentary individuals aged 18-45 years with head forward posture and temporomandibular joint dysfunction (Cranio-Cervico-Mandibular Malalignment). The main questions it aims to answer are:

• Do Scapulothoracic exercises given in addition to cervical posture exercises have an effect on postural stability, proprioception, muscle strength, muscular endurance and mandibular functions in individuals with Cranio-Cervico-Mandibular malalignment?

Researchers will compare conventional neck exercises (control group) and scapulothoracic exercises applied in addition to conventional neck exercises (treatment group) to see the effects of scapulothoracic exercises on the neck and jaw area.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cyprus International University

Mersin, Lefkosa, 99040, Turkey (Türkiye)

About this study

The investigators aimed to investigate the effects of scapulothoracic exercises on postural stability, muscle strength, muscular endurance, mandibular functions and proprioception in sedentary individuals aged 18-45 years with cranio-cervico-mandibular malalignment including head-first posture and temporomandibular joint dysfunction problems.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female students and employees between the ages of 18-45,
  • Individuals with a craniovertabral angle (CVA) <50° and a Fonseca questionnaire score between 20-100,
  • Individuals with a Helkimo clinical dysfunction index score between 1-25,
  • Individuals with a low level of physical activity according to the International Physical Activity Questionnaire.

Exclusion criteria

  • Serious problems of the musculoskeletal system, including the cervical and thoracic spine,
  • Presence of serious chronic diseases such as hypertension, diabetes, cancer,
  • Presence of neurological disease at a level that will affect balance and postural control,
  • Being pregnant,
  • Tooth and jaw problems in the last 6 months,
  • Individuals with a total denture or prosthesis on the anterior teeth.

Treatment and study plan

Exercises

Other

For control group; Cervical conventional exercises. For treatment group; scapulothoracic exercises including strengthening, proprioceptive and stabilization exercises in addition to cervical conventional exercises

Primary outcomes

  1. Postural Stability

    Time frame: Postural stability was measured at 3 different times (before treatment, 8 weeks after treatment, 12 weeks follow up). The average measurement time for each participant was 5 min.

    Five different data were obtained: the peripheral length value of the total sway degree (°) made on the device during balance, the percentile value of the area gap (%) showing the percentage of the area drawn according to the reference circle, the sway velocity value (°/sec), the average values (°) reached in the sway in the antero-posterior (AP) and medio-lateral (ML) directions.

  2. Joint Position Sense

    Time frame: Proprioception measurements were made at 3 different times (before treatment, 8 weeks after treatment, 12 weeks follow up). The mean measurement time for mandibular position sense for each participant was 8 min. Cervical joint position sense measure

    Mandibular and cervical joint position sense measurements were made.

Secondary outcomes

  1. Muscle Strength

    Time frame: Muscle strength measurements were made at 3 different times (pre-treatment, 8th week post-treatment, 12th-week follow-up). The temporomandibular joint depressor muscle strength measurement time for each participant lasted 3 minutes. The st

    Isometric muscle strength test will be performed on TMJ depressor muscles and cervical region muscles.

  2. Endurance Measurement of Deep Neck Flexor Muscles

    Time frame: Muscular endurance of deep neck flexors was measured at 3 different times (pre-treatment, 8th week post-treatment, 12th week post-treatment follow-up). It took an average of 15 minutes for each participant.

    The muscular endurance measurement of the deep neck flexors will be made using the "craniocervical flexion test" and a stabilizer device.

  3. Mandibular Function Disorder Questionnaire (MFBA)

    Time frame: Mandibular Function Disorder Questionnaire (MFBA) was measured at 3 different times (pre-treatment, 8th week post-treatment, 12th week post-treatment follow-up). It took an average of 2 minutes for each participant.

    It is used to evaluate the level of impairment in jaw functions in patients with TMED.

Other outcomes

  1. Body Mass Index

    Time frame: Body Mass Index was measured at pre-treatment period.

    Height and body weights were measured to measure the body mass index of the participants.

Sponsors and collaborators

Lead sponsor

Cyprus International University

Other

Collaborators

  • Eastern Mediterranean University

Registry information

Official study title

The Effects of Scapulothoracic Exercises on Postural Stability, Muscle Strength, Muscular Endurance and Proprioception in Sedentary Individuals With Cranio-Servico-Mandibular Malalignment

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jul 28, 2023
Registry last updated
Aug 2, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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