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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01821014 |
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Date of registration:
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20/03/2013 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Satellite-supplementation of Medical Outreach Clinics: a Feasibility Study
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Scientific title:
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Satellite-supplementation of Medical Outreach Clinics: a Feasibility Study |
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Date of first enrolment:
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February 2013 |
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Target sample size:
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144 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01821014 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Diagnostic
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Phase:
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N/A
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Countries of recruitment
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Honduras
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United States
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Contacts
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Name:
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Bart Demaerschalk, MD/MSc |
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Address:
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Telephone:
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Email:
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Affiliation:
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Mayo Clinic |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Able to give informed consent
- Non-emergent medical complaints
- At least 18 yrs in age
Exclusion Criteria:
- Pregnancy
- Mental Disability
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Developing Countries
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Telemedicine
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Diagnosis
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Therapeutics
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Primary Health Care
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Intervention(s)
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Other: Telemedicine
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Other: In-person physician interaction
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Primary Outcome(s)
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Recommended clinical treatments
[Time Frame: Same Day as clinic visit (less than 6 hours)]
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Clinical Diagnoses
[Time Frame: Same Day as clinic visit (less than 6 hours)]
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Secondary Outcome(s)
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Patient opinions of physician interactions
[Time Frame: Immediately following physician interactions (less than 6 hours)]
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Physician opinions of patient interactions
[Time Frame: immediately following volunteer activities with the clinic (less than 48 hours)]
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Volunteer opinions of physician-patient interactions
[Time Frame: immediately following experience with the clinic (Less than 48 hours)]
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Secondary ID(s)
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13-000132
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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