Healthcare Decisions on Dietary and Environmental Allergen Exposure
Sponsor
Data Collection Analysis Business Management (Other)
Overall Status
Unknown status
CT.gov ID
NCT03144908
Collaborator
PAS Research Services (Other)
200
1
44
4.5
Study Details
Study Description
Brief Summary
Design of this study is to collect data and review Principal Investigators standard operating procedures on allergy testing and changes made to their specific SOP.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
The purpose of this minimal risk observational study is to increase surveillance for dietary and environmental allergens exposure and to also determine targeted risk reducing and preventative strategies.
Study Design
Study Type:
Observational
Actual Enrollment
:
200 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Medical Provider Experience and Assessment on Healthcare Decisions Regarding Dietary and Environmental Allergen Exposure
Actual Study Start Date
:
May 1, 2017
Anticipated Primary Completion Date
:
May 1, 2020
Anticipated Study Completion Date
:
Dec 31, 2020
Outcome Measures
Primary Outcome Measures
- Provider Structures and Processes [36 months]
Plan of Care Changes due to Allergy testing. Provider based observational survey system on the health and well being of patients and populations.
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
- Must be a medical practitioner 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 and family medical history.
Exclusion Criteria:
- Government funded insurance data cannot be included in the study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | DCABM | Land O' Lakes | Florida | United States | 33558 |
Sponsors and Collaborators
- Data Collection Analysis Business Management
- PAS Research Services
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Data Collection Analysis Business Management
ClinicalTrials.gov Identifier:
NCT03144908
Other Study ID Numbers:
- PAS1462
First Posted:
May 9, 2017
Last Update Posted:
Jan 23, 2019
Last Verified:
Jan 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: