Study Results
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.
RECRUITING
67 participants
OBSERVATIONAL
2022-11-02
2024-12-25
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Temporomandibular joint dysfunction group
The group will include patients with temporomandibular joint dysfunction.
Physical assessments
Physical assessments include the presence of joint sounds (yes/no), Fonseca Anamnestic Questionnaire, tenderness/pressure pain threshold rating, muscle strengths assessments, temporomandibular joint and cervical region range of motion measurements, and pain.
Questionnaire
General Health Questionnaire-28 and SF-36 will be apply.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Physical assessments
Physical assessments include the presence of joint sounds (yes/no), Fonseca Anamnestic Questionnaire, tenderness/pressure pain threshold rating, muscle strengths assessments, temporomandibular joint and cervical region range of motion measurements, and pain.
Questionnaire
General Health Questionnaire-28 and SF-36 will be apply.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being in group I according to RDC/TMD Axis I,
Exclusion Criteria
* Having dental problems
* Having any disorder and/or disease involving structures and/or masticatory muscles associated with TMD
* Having a history of trauma in the head and neck region,
* Having previously undergone temporomandibular joint surgery,
* Using corticosteroid and anticonvulsant drugs
* Patients who have received physiotherapy and rehabilitation related to the temporomandibular joint in the last six months
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Afyonkarahisar Health Sciences University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Emel Taşvuran Horata
PhD; Assistant Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
EMEL TAŞVURAN HORATA, PhD
Role: PRINCIPAL_INVESTIGATOR
Afyonkarahisar Health Sciences University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Emel Taşvuran Horata
Afyonkarahisar, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
EMEL TAŞVURAN HORATA, PhD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2022/5
Identifier Type: -
Identifier Source: org_study_id