Use of the My HealtheVet for Health Information Sharing
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT01955005 |
|
Recruitment Status :
Completed
First Posted : October 7, 2013
Results First Posted : January 7, 2016
Last Update Posted : February 5, 2016
|
- Study Details
- Tabular View
- Study Results
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Chronic Illness | Behavioral: My HealtheVet Training Other: Internet Skills Training | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 60 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Health Services Research |
| Official Title: | Pilot of My HealtheVet Training to Improve Co-Managed Care for Veterans |
| Study Start Date : | October 2013 |
| Actual Primary Completion Date : | September 2014 |
| Actual Study Completion Date : | September 2014 |
| Arm | Intervention/treatment |
|---|---|
|
Experimental: My HealtheVet Training
Participants will be asked to watch an on-line training video, review written materials, and print a document containing health information from their My HealtheVet account.
|
Behavioral: My HealtheVet Training
Participants will be asked to watch an on-line training video, review written materials, and print a document containing health information from their My HealtheVet account. |
|
Active Comparator: Internet Skills Training
Participants will review written training materials to learn how to search the Internet for health information and how to decide which Internet sites have good quality information.
|
Other: Internet Skills Training
Participants will review written training materials to learn how to search the Internet for health information and how to decide which Internet sites have good quality information. |
- Percentage of Participants Who Brought Their VA Information From My HealtheVet to Their Visit With Their Non-VA Provider [ Time Frame: Within 1-2 week of non-VA provider visit ]The primary outcome is whether or not the veteran brings their VA information from My HealtheVet to their visit with their non-VA provider. Providers will be asked to complete a form during the appointment where assessment of sharing this information is embedded in a checklist of possible visit activities. Participants will also if they provided this information to the provider in the event the provider opts to not return the form.
- Proportion of Total Number of Unique Medications Discrepant Between VA and Non-VA Medication Lists [ Time Frame: Typically within 1 month of non-VA provider visit ]A medication discrepancy metric was be calculated by comparing the current VA medication list with the non-VA provider medication list to determine the total number of distinct medications. The number of discrepant medications between these lists is the numerator and is divided by the total number of distinct medications on both lists combined. This will yield a range of scores between score between 0 and 1, with 1 indicating perfect agreement between the two lists.
- Proportion of Participants Who Received One or More Duplicate Laboratory Tests in the Non-VA Provider Visit. [ Time Frame: Typically within 1 month of non-VA provider visit ]Therapeutic duplication will be defined as concurrent use of more than one medication from the same therapeutic class. For laboratory duplication, we will review non-VA and VA medical records 6 months prior to the non-VA provider visit. Each patient will be assigned a dichotomous indicator for whether they received therapeutic duplication and/or laboratory duplication during their non-VA provider visit
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Upcoming Non-VA provider appointment
- Take 5 or more prescribed medications
- Have or obtain a My HealtheVet premium account
- Access to computer, printer, & Internet to complete study protocol
Exclusion Criteria:
- No non-VA provider or upcoming appointment
- Less than 5 medications
- No premium MHV account
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01955005
| United States, Iowa | |
| Iowa City VA Health Care System, Iowa City, IA | |
| Iowa City, Iowa, United States, 52246-2208 | |
| Principal Investigator: | Carolyn L Turvey, PhD MS | Iowa City VA Health Care System, Iowa City, IA |
| Responsible Party: | VA Office of Research and Development |
| ClinicalTrials.gov Identifier: | NCT01955005 |
| Other Study ID Numbers: |
PPO 13-178 |
| First Posted: | October 7, 2013 Key Record Dates |
| Results First Posted: | January 7, 2016 |
| Last Update Posted: | February 5, 2016 |
| Last Verified: | January 2016 |
|
Health Records, Personal Delivery of healthcare Consumer Participation Internet |
|
Chronic Disease Disease Attributes Pathologic Processes |

