Arrythmia Clinical Trial
Official title:
Telemedicine Enabling Patients in Self-care Behaviors
Verified date | September 2021 |
Source | University of Michigan |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the study is to see if monthly telemedicine computer visits (visits using the computer) improve the time it takes to identify and treat an arrhythmia. The second purpose is to see if monthly telemedicine computer visits improves the participant's understanding of the arrhythmia and improves how the participant feels with daily activities.
Status | Completed |
Enrollment | 60 |
Est. completion date | September 20, 2021 |
Est. primary completion date | August 10, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Read and speak English - 18 years of age or older - Have a cardiac arrhythmia diagnosis - Are willing to participate in the study and answer a pre and post survey. Exclusion Criteria: - Any difficulty in understanding the study - Does not have internet or a cell phone data plan - Any life threatening arrhythmias - Objection to working with nurse practitioners and physician assistants |
Country | Name | City | State |
---|---|---|---|
United States | University of Michigan | Ann Arbor | Michigan |
Lead Sponsor | Collaborator |
---|---|
University of Michigan |
United States,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time of recognition of an arrhythmia | Patient recognition of a probable arrhythmia | Up to 6 months | |
Primary | Time of diagnosis of arrhythmia | Time of diagnosis of arrhythmia by medical staff- at what point is the diagnosis present. | Up to 6 months | |
Primary | Time to treatment initiation of arrhythmia | The time- what point in time is the treatment plan innitiated | Up to 6 months | |
Secondary | Change in self efficacy in medication use score as measured by the Medication Self Efficacy Tool (MUSE) survey | MUSE is 7 items which are evaluated to identify if the patient has a good overall understanding and perception of their medicine. | Baseline, 6 months | |
Secondary | Change in functioning self efficacy score as measured by the 13 Item Shortened Function Self-efficacy Scale (FSES) | The FSES is 13 questions with responses scored from 1 to 5 with a maximum score of 65. Higher scores indicates higher level of functioning. | Baseline, 6 months | |
Secondary | Change in self-efficacy of arrhythmia management score as measured by the Arrhythmia-Specific questionnaire in Tachycardia and Arrhythmias (ASTA) survey | The ASTA questionnaire is divided into three separate parts.
Part 1 is descriptive data that evaluates the patient's latest episode of arrhythmia and his/her pharmaceutical treatment. Part 2 has 9 items and a four point's response scale with response alternatives from 0 to 3: "No (0), Yes, to a certain extent (1), Yes, quite a lot (2) or Yes, a lot (3) ". A summarized score is calculated for the items, a higher score implies higher symptom burden due to the heart rhythm disturbance. Scoring for the ASTA symptom burden scale ranges from 0 (least burdensome) to highest 27 (most burdensome). Part 3 scale has 13 items and describes the arrhythmia's influence on daily life with a seven items physical subscale (items 1-5, 10 and 12) and a six items mental subscale (items 6-9, 11 and 13). The response alternatives from 0 to 3: "No (0), Yes, to a certain extent (1), Yes, quite a lot (2), |
Baseline, 6 months |
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