Pain, Central Sensitization and Psychoemotional State in Patients With Chronic Masticatory Muscle Pain

Sponsor
Wroclaw Medical University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05676827
Collaborator
(none)
102
24

Study Details

Study Description

Brief Summary

The aim of this study is to investigate the relationship of psychological aspects, selected blood parameters, pain, central sensitization, and muscle electromyography activity in patients with chronic masticatory muscle pain.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Diagnostic Criteria for Temporomandibular Disorders Clinical Examination
  • Diagnostic Test: Blood test

Detailed Description

In this prospective cohort study, the study group will consist of 51 people with masticatory muscle pain lasting longer than 3 months, while the control group will involve 51 people without such disorder.

Muscle type of temporomandibular disorders will be diagnosed on the basis of validated and standardized DC/TMD protocol.

Additionally potential headaches will be assessed according to the ICHD-3, since coexistence of chronic masticatory muscle pain and headache is often observed.

Psychological aspects will be analyzed using validated questionnaires regarding depression (PHQ-9), anxiety (GAD-7), perceived stress (PSS-10), satisfaction with life (SWLS), type D personality (DS-14) and coping with stress (Mini-COPE). Central Sensitization will be assessed using the Central Sensitization Index and determination of following blood substances: serotonin, dopamine, acetylcholine, adrenaline, noradrenaline, cortisol, parathyroid hormone, CRP, fibrinogen, interleukin 1B, interleukin 6 and interleukin 8. Additionally the level of electrolytes in the blood (Mg, Ca, Na, K) and level of phosphate will be measured.

Pain assessment will be done using a validated and standardized questionnaire regarding chronic pain (GCPS) and an algometer and will include the measurement of pressure pain threshold in masseter and temporal muscles. In addition, potential autonomic disorders will be assessed using Autonomic Symptoms Questionnaire proposed by Low. Electromyographic muscle activity will be assessed by tetany test. The results of the study will allow for deeper understanding of the complex nature of orofacial pain of muscle origin and its connection with the mechanism of central sensitization, headache and muscle electromyographic activity. Measurement of blood parameters will provide more accurate information on the pathophysiology of these disorders and the use of validated questionnaires will provide valuable information about the mental state of patients.

Study Design

Study Type:
Observational
Anticipated Enrollment :
102 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Assessment of the Relationship Between Pain, Central Sensitization and Psychoemotional State in Patients With Chronic Masticatory Muscle Pain
Anticipated Study Start Date :
Jan 4, 2023
Anticipated Primary Completion Date :
Jan 4, 2024
Anticipated Study Completion Date :
Jan 4, 2025

Arms and Interventions

Arm Intervention/Treatment
Study group

Participants with masticatory muscle pain lasting for over 3 months.

Diagnostic Test: Diagnostic Criteria for Temporomandibular Disorders Clinical Examination
Clinical examination made by experienced dentists (minimum 5 years of practice) and trained and calibrated in accordance with the protocol available on the DC/TMD.

Diagnostic Test: Blood test
Blood samples will be tested to investigate two polymorphisms of genes encoding proteins for serotonin receptors HTR2A - rs4941573 in intron 3 and dopamine DRD3 - rs6280 (Ser9Gly) and levels of serotonin, dopamine, C-reactive protein, cortisol, sodium, potassium, and calcium.

Control group

Participants without masticatory muscle pain in last 6 months.

Diagnostic Test: Diagnostic Criteria for Temporomandibular Disorders Clinical Examination
Clinical examination made by experienced dentists (minimum 5 years of practice) and trained and calibrated in accordance with the protocol available on the DC/TMD.

Diagnostic Test: Blood test
Blood samples will be tested to investigate two polymorphisms of genes encoding proteins for serotonin receptors HTR2A - rs4941573 in intron 3 and dopamine DRD3 - rs6280 (Ser9Gly) and levels of serotonin, dopamine, C-reactive protein, cortisol, sodium, potassium, and calcium.

Outcome Measures

Primary Outcome Measures

  1. Relationship between masticatory muscle pain and polimorphism of serotonin receptor gene HTR2A - rs4941573 and dopamine receptor gene DRD3 - rs6280 [January 3, 2023 - January 3, 2024]

    Each participant will undergo genetical blood test.

  2. Relationship between masticatory muscle pain and serotonin and dopamine levels. [January 3, 2023 - January 3, 2024]

    Each participant will undergo blood test.

  3. Relationship between masticatory muscle pain and magnesium, sodium, potasium and calcium levels. [January 3, 2023 - January 3, 2024]

    Each participant will undergo blood test.

  4. Relationship between masticatory muscle pain and cortisol level. [January 3, 2023 - January 3, 2024]

    Each participant will undergo blood test.

  5. Relationship between masticatory muscle pain and CRP level. [January 3, 2023 - January 3, 2024]

    Each participant will undergo blood test.

Secondary Outcome Measures

  1. Relationship between masticatory muscle pain and depression assessed by Patient Health Questionnaire. [January 3, 2023 - January 3, 2024]

    Each participant will fill in Patient Health Questionnaire - 9. PHQ-9 total score for the nine items ranges from 0 to 27.Scores of 5, 10, 15, and 20 represent cutpoints for mild, moderate, moderately severe and severe depression, respectively.

  2. Relationship between masticatory muscle pain and PPTs. [January 3, 2023 - January 3, 2024]

    Participants from study group will be tested using algometer to determine pressure pain threshold in masseter muscle and temporal muscle.

  3. Relationship between masticatory muscle pain and anxiety assessed by Generalized Anxiety Disorder -7. [January 3, 2023 - January 3, 2024]

    Each participant will fill in Generalized Anxiety Disorder -7 that consists of 7 items. Total score ranges 0-21 points. Scores of 5, 10, and 15 are taken as the cut-off points for mild, moderate and severe anxiety, respectively.

  4. Relationship between masticatory muscle pain and perceived stress assessed by Perceived Stress Scale. [January 3, 2023 - January 3, 2024]

    Each participant will fill in Perceived Stress Scale -10. Scores are obtained by reversing the scores on the four positive items, e.g., 0=4, 1=3, 2=2, etc. and then summing across all 10 items. Items 4,5, 7, and 8 are the positively stated items. It can range from 0 to 40. Scores ranging from 0-13 would be considered low stress,14-26 would be considered moderate stress, 27-40 would be considered high perceived stress.

  5. Relationship between masticatory muscle pain and satisfaction with life assessed by Satisfaction With Life Scale. [January 3, 2023 - January 3, 2024]

    Each participant will fill in Satisfaction With Life Scale which consist of five questions with 5 possible answers. Total score range is 35. Higher score represents higher life satisfaction. Score ranging from 5-9 as considered as extremly dissatisfied with life, 10-14 dissatisfied, 15-19 slightly dissatisfied, 20-24 slightly satisfied, 25-29 satisfied, 30-35 extremely satisfied.

  6. Relationship between masticatory muscle pain and Type D personality assessed by DS-14 quesstionaire. [January 3, 2023 - January 3, 2024]

    Each participant will fill DS-14 questionnaire which contains 14 Likert-style questions. Each questions has a score range of 0-4. This questionnaire consist of two subscales: negative affectivity and Social Inibition. A cut-off of 10 on both scales is used to classify subject as type-D personality. Maximum score in both scales is 28.

  7. Relationship between masticatory muscle pain and coping with stress assessed by mini COPE. [January 3, 2023 - January 3, 2024]

    Each participant will fill in mini COPE. Questionnaire consists of 28 statements that make up 14 stress coping strategies.Some testing strategies were divided into four categories and corresponding strategies (inventory scales): active coping (including: active coping, planning, positive reevaluation), helplessness (including: taking psychoactive substances, cessation of actions, blaming self), seeking support (including: seeking emotional support, seeking instrumental support), avoidance behaviors (including dealing with something else, denying, discharging). three strategies create independent factors (turning to religion, acceptance, sense of humor). The range of results for each statement ranges from 0 to 3 points. The calculation of the results consists in adding to each other points for the answers regarding two theorems that make up the given scale, and then dividing by 2.

  8. Relationship between masticatory muscle pain and central sensitization assessed by Central Sensitization Inventory. [January 3, 2023 - January 3, 2024]

    Each participant will fill in Central Sensitizatin Inventory. This questionnaire consist of two parts. First part includes 25 questions regarding common central sensitivity symptoms. It allows to categorize participant into one of five categories: subclinical (0-29), mild (30-39), moderate (40-49), severe (50-59), and extreme (60-100) Second part is not scored, but it determines if the participant has been diagnosed with certain CSS disorders or related disorders.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria for study group:
  • Masticatory muscle pain for at least 3 months, based on DC/TMD, at least 18 y.o
Exclusion Criteria:
  • severe neurological or psychiatric diseases, use of drugs that may affect the neuromuscular system, alcohol or drug addiction, cancer or pregnancy, previous head surgery
Inclusion criteria for control group:
  • no pain in masticatory muscles, age of at least 18 y.o Exclusion criteria the same as for study group

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Wroclaw Medical University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Joanna Smardz, Investigator, Wroclaw Medical University
ClinicalTrials.gov Identifier:
NCT05676827
Other Study ID Numbers:
  • WMU1/2022
First Posted:
Jan 9, 2023
Last Update Posted:
Jan 9, 2023
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Joanna Smardz, Investigator, Wroclaw Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 9, 2023