Physical Therapy Interventions Relative to Dental Treatment in Individuals With Bruxism

NCT ID: NCT01778881

Last Updated: 2016-10-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-03-31

Study Completion Date

2016-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Bruxism is a parafunctional habit characterized by grinding and/or clenching of the teeth. It may happen while awake (awake bruxism) or while sleeping (sleep bruxism). In adults, the prevalence is 20% for the awake bruxism and 8% for the sleep bruxism. Peripheral, central, and psychosocial factors influence the disorder, which may predispose to pain in the masticatory muscles and neck, headache, decreased pain thresholds in the masticatory and cervical muscles, limitation mandibular opening, sleep disorders, stress, anxiety, depression, and overall impairment of oral health. The aim of this study is to compare physical therapy interventions with dental treatment in pain, mandibular opening, sleep quality, anxiety, stress, depression, and oral health in individuals with bruxism.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Participants will be randomized into one of four groups: Group 1 (n = 24) intervention will consist of massage and stretching exercises; Group 2 (n = 24) will consist of relaxation and imagination therapies; Group 3 (n = 24) will receive dental treatment and Group 4 (n=24) will consist of massage, exercises, relaxation and imagination. The evaluations will be performed at baseline, immediately after treatment, and at 2-month follow-up. Pain intensity will be assessed using the visual analogical scale, while pain thresholds will be determined using algometry. Mandibular opening will be assessed using digital pachymeter. Sleep quality will be assessed by the Pittsburgh Sleep Quality Index, anxiety by the State-Trait Anxiety Inventory, stress by the Perceived Stress Scale-10, depression by the Beck Depression Inventory, and oral health will be assessed using the Oral Health Impact Profile - 14. Significance level will be determined at the 5% level.

Valid Reasons of updates:

2014 - Changes made according requeriments of plattform of ClinicalTrials.

2015 - In 2014, in my qualification examination at University of São Paulo, the professors suggested my transfer from master degree to direct doctorate and the inclusion of more one intervention group, whereas the other three groups were still in the randomization process. I updated the registration in 2015 with the inclusion of this fourth group. However, as the protocol published in 2014 reports 3 groups (initial idea of the master degree before the transition to the direct doctorate), this fourth group started the treatment (massage, exercises, relaxation and imagination) after the end of treatment of other three groups (Groups:1,2 and 3).

2016- Although I have listed as primary variables: pain (VAS) and mandibular opening in this platform in 2013, and in the protocol published in 2014 (http://trialsjournal.biomedcentral.com/articles/10.1186/1745-6215-15 -8); symptoms like clenching, headaches and sleep difficulties were also assessed by VAS, and no included posteriorly to trial registration. They were evaluated, but not described in this platform. The same happened with intention to treat analysis.

June 20, 2016- Updates for clarifications and suggested by the PRS Team.

Please, any doubts, send me a e-mail! Thank you!

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Bruxism

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Bruxism Physical therapy modalities Massage Muscle stretching exercises Relaxation therapy Imagination

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Massage + Exercise

Massage and stretching exercises

Group Type EXPERIMENTAL

Massage and stretching exercises

Intervention Type OTHER

The routine to be used in this group (stretching, massage, and diaphragmatic breathing).

Relaxation +Imagination

Relaxation and Imagination therapies

Group Type EXPERIMENTAL

Relaxation and imagination therapies

Intervention Type OTHER

The routines to be adopted will focus on progressive muscle relaxation associated to imagination and diaphragmatic breathing.

Dental treatment

Reconstruction with composite resin

Group Type EXPERIMENTAL

Dental treatment

Intervention Type OTHER

Restoring treatment will involve direct reconstruction of the anterior guides (incisive faces of the incisive and canine teeth) with resin.

Massage + Exercise + Relaxation + Imagination

Massage, stretching exercises, relaxation and imagination

Group Type EXPERIMENTAL

Massage, exercises, relaxation and imagination therapies

Intervention Type OTHER

The routine to be used in this group (stretching, massage, diaphragmatic breathing, progressive muscle relaxation and imagination therapies).

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Massage and stretching exercises

The routine to be used in this group (stretching, massage, and diaphragmatic breathing).

Intervention Type OTHER

Relaxation and imagination therapies

The routines to be adopted will focus on progressive muscle relaxation associated to imagination and diaphragmatic breathing.

Intervention Type OTHER

Dental treatment

Restoring treatment will involve direct reconstruction of the anterior guides (incisive faces of the incisive and canine teeth) with resin.

Intervention Type OTHER

Massage, exercises, relaxation and imagination therapies

The routine to be used in this group (stretching, massage, diaphragmatic breathing, progressive muscle relaxation and imagination therapies).

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Sleep Bruxism identified by the interview, clinical assessment and diagnostic criteria of the International Classification for Sleep Disorders (ICSD) of the American Academy of Sleep Medicine (AASM);
* Awake bruxism identified by the interview, clinical assessment and questionnaire of Pintado;
* Aged between 18 to 60 years;
* A minimum pain intensity score of 3 on the Visual Analogical Scale.

Exclusion Criteria

* More than two missing teeth, except third molars;
* Systemic and/or degenerative diseases;
* Arthrogenic or mixed temporomandibular disorder (TMD) according to the Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD), axis I;
* Neurological or psychiatric diseases (with the exception of anxiety and depression);
* Using medications that influence sleep or motor behavior;
* Periodontal disorders;
* Abuse of alcohol and/or illicit drugs;
* Removable dentures, superior and/or inferior;
* Total dentures;
* Direct trauma or past surgery in the orofacial region;
* On physical, speech, dental, or psychological therapy at the time of study entry.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Sao Paulo General Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Amélia P Marques, PhD

Role: STUDY_DIRECTOR

University of Sao Paulo

Cinthia SM Amorim, MSc

Role: PRINCIPAL_INVESTIGATOR

University of Sao Paulo

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Medicine School of the University Of São Paulo

São Paulo, São Paulo, Brazil

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Brazil

References

Explore related publications, articles, or registry entries linked to this study.

Santos Miotto Amorim C, Firsoff EF, Vieira GF, Costa JR, Marques AP. Effectiveness of two physical therapy interventions, relative to dental treatment in individuals with bruxism: study protocol of a randomized clinical trial. Trials. 2014 Jan 7;15:8. doi: 10.1186/1745-6215-15-8.

Reference Type DERIVED
PMID: 24398115 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

cinthiamiotto

Identifier Type: -

Identifier Source: org_study_id