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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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28 November 2016 |
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Main ID: |
NCT02970461 |
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Date of registration:
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15/11/2016 |
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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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Gamifying Patient's Personal Data Validation and Completion in a Personal Health Record
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Scientific title:
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Gamifying Patient's Personal Data Validation and Completion in a Personal Health Record |
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Date of first enrolment:
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July 2016 |
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Target sample size:
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40000 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02970461 |
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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: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Argentina
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Contacts
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Name:
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Carlos Bonofiglio, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Hospital Italiano de Buenos Aires |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients enrolled in the Hospital Italiano de Buenos Aires system who are over 18
years old
- Patients who are registered in Hospital Italiano de Buenos Aires' Personal Health
Record
- Patients whose use of the Personal Health Record during the previous year exceeds the
median of use
Exclusion Criteria:
- Refusal to participate or to the informed consent process
- Subjects with a record of Obsessive Compulsive Disorders or related condition as per
DSM IV
- Subjects with a record of Neurological conditions that could impair reading (aphasia,
dementia, etc)
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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Chronic Disease
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Intervention(s)
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Other: Gamified Group
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Other: Control Group
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Primary Outcome(s)
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Change in Number of Completed Fields
[Time Frame: Measured at baseline, 30 days after and 6 months after]
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Secondary Outcome(s)
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Change in Number of Validated Fields
[Time Frame: Measured at baseline, 30 days after and 6 months after]
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Change in Number of Corrected Fields
[Time Frame: Measured at baseline, 30 days after and 6 months after]
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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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