Identifying Which Adverse Events Associated With Dry Needling Should be Included For Informed Consent: A Modified e-Delphi Study
Completed
Conditions studied: Dry Needling
In brief
Dry Needling is an intervention that continues to gain widespread interest as a treatment adjunct for various pathological conditions. With the increased use of dry needling in the clinic, there comes a need for additional research to investigate the adverse events associated with the use of dry needling. Informed Consent is a process that is legally required in many states prior to the performance of a treatment intervention like dry needling. It is important therefore to identify which of these adverse events should be included in an informed consent process.
Key facts
- Study ID
- NCT05300815
- Run by
- Youngstown State University
- People needed
- 39
- Starts
- 2022-03-02
- Expected to finish
- 2022-07-31
- Last updated by the study team
- 2023-06-13
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Physical Therapists who:
- Have >= 7 years of clinical practice performing dry needling and at least ONE of the following secondary criteria:
- Certification in Dry Needling
- Completion of a manual therapy fellowship that included dry needling training
- >= 1 total scholarly product (poster presentation, author of a peer-reviewed publication)
You may not qualify if…
- Not a Physical Therapist
- Has less than 7 years experience in dry needling
- Does not meet the secondary criteria established in the inclusion criteria
Where it is running
- Youngstown State University — Youngstown, Ohio, United States
Full record on ClinicalTrials.gov
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