Hypertension Clinical Trial
Official title:
An Intervention to Increase Engagement With Hypertension Care for American Indian Patients
NCT number | NCT04414982 |
Other study ID # | 15-1711 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 1, 2015 |
Est. completion date | June 30, 2020 |
Verified date | August 2020 |
Source | University of Colorado, Denver |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this study is to reduce the effects of stereotype threat on the adherence of
American Indian/Alaska Native patients with hypertension.
The specific aims of this study, which employs a values affirmation intervention, are to:
1. Compare the effects of the values-affirmation exercise with a control exercise in AI/AN
patients with hypertension.
2. Compare the effects of the values-affirmation exercise in AI/AN patients with its
effects in white patients.
Status | Completed |
Enrollment | 339 |
Est. completion date | June 30, 2020 |
Est. primary completion date | June 30, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility |
Inclusion Criteria: - Hypertension diagnosis: primary or secondary ICD-10 code diagnosis in last 24 mo - SBP >160 mm Hg or DBP >90 mm Hg in last 12 months - Currently taking antihypertensive medications - Medications filled within health system's pharmacy - White or American Indian/Alaska Native, self-reported race - Upcoming primary care visit - Ability to read and write English - History of hypertension defined as having an outpatient visit in the past year with a primary or secondary ICD-9 code diagnosis of hypertension, with the diagnosis of hypertension confirmed by review of the patient's medical record before enrollment. - Additional inclusion criteria are age >18 years - Use of Denver Indian Health and Family Services (DIHFS) or Denver Health (DH) as their usual source of care. - American Indian/Alaska Native as defined by DIHFS uses to define eligibility for no-cost services. - To define the comparator group at DH we will use self-described race/ethnicity of white/non- Latino. - All eligible patients must have the ability to provide informed consent. Exclusion Criteria: - Pregnancy-related hypertension - Dialysis-dependent end-stage renal disease - Patients who cannot speak or write English - Unable to provide consent |
Country | Name | City | State |
---|---|---|---|
United States | Denver Health and Hospital Authority | Denver | Colorado |
United States | Denver Indian Health and Family Services | Denver | Colorado |
Lead Sponsor | Collaborator |
---|---|
University of Colorado, Denver | American Heart Association, Denver Health and Hospital Authority, Denver Indian Health and Family Services, University of Colorado Centers for American Indian and Alaska Native Health |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Antihypertensive Medication Adherence using Pharmacy Records | This antihypertensive medication adherence outcome will be a summary measure of adherence which assesses the proportion of days covered (PDC) over the period of observation for which a patient obtains antihypertensive medications. Adherence will be calculated for each antihypertensive drug in the regimen and combined across drugs into a summary measure of adherence for the entire drug regimen. | Baseline, 3 and 6 months | |
Primary | Change in Antihypertensive Medication Adherence using Self-Reported Adherence | This antihypertensive medication adherence outcome will be a summary measure of self-reported adherence using the validated Voils instrument, which has 3 questions that address adherence over the previous 7 days. | Baseline, 3 and 6 months | |
Primary | Change in Antihypertensive Medication Adherence using Pill Counts | This antihypertensive medication adherence outcome will be a summary outcome measure of adherence where if x is the number of pills in the bottle, y is the number of pills that would have been in the bottle had all pills been taken since the bottle was filled, and z is the number of pills that should have been taken since the last fill, and adherence is calculated as 1- [(x-y)/z]. | Baseline, 3 and 6 months | |
Secondary | Systolic Blood Pressure | Systolic blood pressure over time. | Baseline, 3 and 6 months | |
Secondary | Proportion of Time Blood Pressure is Under Control | Defined as the proportion of time over the 6-months of follow-up with a BP = 160/90 mmHg | 6 months |
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