Pain Management Clinical Trial
Official title:
Clinical Researcher Experience Assessment Documenting Usage and Plan of Care Changes Due to Drug Screenings ©
Verified date | January 2019 |
Source | Data Collection Analysis Business Management |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this minimal risk, observational survey is to document the accuracy, benefits, and how qualitative and quantitative results affect patients' plan of care.
Status | Enrolling by invitation |
Enrollment | 2000 |
Est. completion date | October 2020 |
Est. primary completion date | October 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 64 Years |
Eligibility |
Inclusion Criteria: - Must be a Medical Practioner - Medical Doctor (MD) - Doctor of Osteopathic (DO) - Physician Assistant (PA) - Advanced Practice Registered Nurse (APRN) - Nurse Practioner (NP) - Must have a current standard operating procedure that includes obtaining/reviewing medical history. Exclusion Criteria: - Government-funded insurance data cannot be included in the study. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Data Collection Analysis Business Management | PAS Research Services |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Plan of Care Changes due to Drug Screenings | Provider based observational survey | 3 years |
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---|---|---|---|
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