- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05882838
The Level of Knowledge and Awareness of Myofascial Pain Syndrome in the Turkish Population
May 21, 2023 updated by: Mustafa Hüseyin Temel, Uskudar State Hospital
This study aimed to assess the level of knowledge and awareness of myofascial pain syndrome (MPS) among the Turkish population.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The study will employ a cross-sectional design to assess the level of knowledge and awareness of myofascial pain syndrome (MPS) in the Turkish population.
A representative sample of individuals will be selected for participation in the survey.
A structured questionnaire will be developed specifically for this study, consisting of questions related to the understanding, recognition, and management of MPS.
The questionnaire will be administered through face-to-face interviews.
Data collected from the survey will be analyzed using appropriate statistical methods to determine the overall level of knowledge and awareness of MPS among the Turkish population.
Study Type
Observational
Enrollment (Estimated)
85
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mustafa H Temel, M.D.
- Phone Number: +905342714872
- Email: mhuseyintemel@gmail.com
Study Contact Backup
- Name: Fatih Bağcıer, M.D.
- Phone Number: 05442429042
- Email: bagcier_42@hotmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients who applied to the physical medicine and rehabilitation outpatient clinic and gave consent to participate in the study.
Description
Inclusion Criteria:
- Giving consent.
Exclusion Criteria:
- Not giving consent.
- Any illness or disability that can prevent filling out the form or communicating.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients admitted to the physical medicine and rehabilitation outpatient clinic.
Patients admitted to the physical medicine and rehabilitation outpatient clinic and gave consent to participate.
|
Myofascial Pain Syndrome Knowledge and Awareness Questionnaire is a questionnaire consisting of a total of 14 questions created by the researchers who are specialized in the field.
The correct answer to each question is one point.
A high score indicates a high level of knowledge and awareness, while a low score indicates a low level of awareness and knowledge.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Level of Knowledge and Awareness of Myofascial Pain Syndrome in the Turkish Population
Time Frame: 1 day
|
By using the data gained with the Myofascial Pain Syndrome Knowledge and Awareness Questionnaire and using the suggested statistical methods by the statistics expert, this study will aim to determine the level of knowledge and awareness of myofascial pain syndrome in the Turkish population.
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mustafa H Temel, M.D., Uskudar State Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
November 1, 2023
Primary Completion (Estimated)
July 1, 2024
Study Completion (Estimated)
November 1, 2024
Study Registration Dates
First Submitted
May 21, 2023
First Submitted That Met QC Criteria
May 21, 2023
First Posted (Actual)
May 31, 2023
Study Record Updates
Last Update Posted (Actual)
May 31, 2023
Last Update Submitted That Met QC Criteria
May 21, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MPSK1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
The individual participant data will be shared upon reasonable request by the corresponding author.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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