Medication Adherence Clinical Trial
Official title:
Impact of Telehealth Warfarin Education on Patient Retention
NCT number | NCT03650777 |
Other study ID # | 015-284 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | February 18, 2016 |
Est. completion date | July 31, 2017 |
Verified date | January 2019 |
Source | Baylor Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this study is to evaluate the effectiveness of telehealth warfarin education in a charity outpatient clinic. The purpose is to increase patient knowledge with regard to their warfarin therapy and to measure knowledge retention
Status | Completed |
Enrollment | 18 |
Est. completion date | July 31, 2017 |
Est. primary completion date | July 31, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Age > 18 years 2. English as a first language 3. Currently taking warfarin for an approved indication 4. Having the ability to see, read, and hear for verbal, written, and iPad® warfarin education Exclusion Criteria: 1. Age < 18 years 2. Unwilling to receive iPad counseling 3. Cognitive dysfunction and impairments that prevents patient from fully comprehending warfarin education |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Baylor Research Institute |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Knowledge Retention of Warfarin Education post video watching | Difference in pre warfarin education video and post video test for warfarin education in patients receiving warfarin education via iPad | pre and post video test(20 minutes) | |
Primary | Long Term Knowledge Retention of warfarin education post video watching | Difference in pre video test and follow up retention test for warfarin education in patients receiving warfarin education via iPad | initial and follow up visit (max 30 days) | |
Secondary | Self Reported Adherence to Warfarin therapy during duration of study | Descriptive results of patient self reported adherence (yes/no response) related to warfarin between initial and follow up visit | Between initial and follow up visit ( max 30 days) | |
Secondary | Satisfaction Survey | A satisfaction survey (designed by pharmacy resident) with 4 questions based on Likert scale (0-5), and one free response question patient completes on follow up visit. Name of Scale used for 4 questions: Likert. (Range 1-5, 1= highly disagree, 2= disagree, 3-neutral, 4-agree, 5-highly agree). There was no total of scoring, each response was individual of each other. | Max 30 days | |
Secondary | Adverse Events | Descriptive results of patient self reported adverse events related to warfarin between initial and follow up visit | Between initial and follow up visit ( max 30 days) | |
Secondary | Time of Warfarin in Therapeutic Range for Duration of Study | Time patient was within therapeutic range for their INR goal between initial and follow up visit | Between initial and follow up visit ( max 30 days) |
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