- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04326608
Psycho-social Aspects After a Physiotherapy Intervention in Chronic TMD Pain
March 26, 2020 updated by: Gema Serrano-Hernanz, Universidad Complutense de Madrid
How patients psycho-social factors change after a physical intervention in patients with chronic TMD pain
Study Overview
Study Type
Observational
Enrollment (Anticipated)
70
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: Gema Serrano-Hernanz, PhD
- Phone Number: 669332986
- Email: gema.serrano.hernanz@gmail.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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Chronic TMD pain
Description
Inclusion Criteria:
- Chronic myofascial TMD pain
Exclusion Criteria:
- Neurologic pain
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
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
TSK-11
Time Frame: immediately after treatment
|
Tampa Scale for Kinesiophobia
|
immediately after treatment
|
TSK-11
Time Frame: at 3 months
|
Tampa Scale for Kinesiophobia
|
at 3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
September 1, 2020
Primary Completion (Anticipated)
January 1, 2021
Study Completion (Anticipated)
April 1, 2021
Study Registration Dates
First Submitted
March 19, 2020
First Submitted That Met QC Criteria
March 26, 2020
First Posted (Actual)
March 30, 2020
Study Record Updates
Last Update Posted (Actual)
March 30, 2020
Last Update Submitted That Met QC Criteria
March 26, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- Geserrher
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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