- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05854446
Delphi Study on Myofascial Pain Syndrome Challenges in Turkey: Patient Journey, Burden, Diagnosis & Treatment Needs.
May 2, 2023 updated by: Mustafa Hüseyin Temel, Uskudar State Hospital
Navigating the Challenges of Myofascial Pain Syndrome in Turkey: A Delphi Methodology Study on Patient Journey, Disease Burden, and Unmet Diagnosis and Treatment Needs
Myofascial pain syndrome is a chronic pain disorder that affects many people in Turkey.
This research study aims to explore the challenges faced by patients with myofascial pain syndrome in Turkey, including the disease burden, patient journey, and unmet diagnosis and treatment needs.
The study will utilize the Delphi methodology, which involves gathering input from a panel of experts over multiple rounds to achieve consensus on the topic.
The results of this study will shed light on the current state of myofascial pain syndrome management in Turkey and provide insights into the areas where improvements can be made.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The study will use a Delphi methodology to investigate the challenges faced by patients with myofascial pain syndrome in Turkey.
A panel of 20 experts with diverse backgrounds in healthcare and pain management will be selected.
The study will be conducted in three rounds, with the first round consisting of open-ended questions to identify key themes related to the disease burden, patient journey, and unmet needs.
In the second round, experts will rate the importance of each theme, and in the third round, they will review the results of the previous round and provide additional feedback.
Data will be analyzed using content analysis and descriptive statistics to identify the areas of consensus and divergence among the experts.
Study Type
Observational
Enrollment (Anticipated)
20
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
Yes
Sampling Method
Non-Probability Sample
Study Population
A panel of 20 experts from diverse backgrounds in healthcare and pain management.
Description
Inclusion Criteria:
- Being an expert on healthcare.
- Giving consent.
Exclusion Criteria:
- Not giving consent.
- Any disorder or condition that may negatively affect reading, comprehension, and form filling.
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 |
---|---|
Healthcare Experts
Experts with diverse backgrounds in healthcare and pain management.
|
In this survey, The experts will be asked open-ended questions based on the literature research and patient surveys carried out by the researchers in the first round to identify key themes related to myofascial pain syndrome, including the disease burden, patient journey, and unmet diagnosis and treatment needs.
In subsequent rounds, the experts will rate the importance of each theme and provide additional feedback.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Identification of areas of agreement and disagreement among experts.
Time Frame: 1 month
|
Data will be analyzed using content analysis and descriptive statistics to identify the areas of consensus and divergence among the experts.
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Anticipated)
June 1, 2023
Primary Completion (Anticipated)
October 1, 2023
Study Completion (Anticipated)
December 1, 2023
Study Registration Dates
First Submitted
May 2, 2023
First Submitted That Met QC Criteria
May 2, 2023
First Posted (Estimate)
May 11, 2023
Study Record Updates
Last Update Posted (Estimate)
May 11, 2023
Last Update Submitted That Met QC Criteria
May 2, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MPS1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Individual participant data will be shared by the corresponding author upon reasonable request.
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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