HypertensionCHAR2NCT03872856
Blood Pressure-Improving Control Among Alaska Native People" (BP-ICAN)
A study testing BP-ICAN in people with Hypertension, run by Southcentral Foundation at 2 sites in United States.
Trial summary
"Blood Pressure: Improving Control among Alaska Native People" (BP-ICAN) that targets blood pressure control among Alaska Native and American Indian (AN/AI) people diagnosed with hypertension. Participants will include adults with a diagnosis of hypertension who have not achieved blood pressure control. Read more about this study
- Who is it for?
- Ages 18 years and older, men only
- Conditions the study is for
- Hypertension
- What is being tested?
- BP-ICAN
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 164 participants
- Where
- 2 sitesUnited States
- Study dates
- 19 Feb 2019to 30 Sep 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Men only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- At least one visit to SCF providers or Community Health Aides within the previous year
- Alaska Native or American Indian
- At least 18 years old
- Meet one of the following two conditions:
- Hypertension diagnosis and 1 systolic blood pressure (SBP) >= 140 mmHg in past 24 months in EHR, AND
- SBP >= 140 mmHg at research visit or from the mean of BP measures during the home screening period, OR
Show all 13Show fewer
- SBP 130-139 mmHg at research visit or from the mean of BP measures during the home screening period plus at least one comorbid condition as stated in American Heart Association guidelines (cardiovascular disease, heart failure, stroke, atrial fibrillation, chronic kidney disease, kidney transplant, or diabetes) II. No hypertension diagnosis but 1 SBP >= 140 mmHg in past 18 months in EHR, AND
- <!-- -->
- SBP >=140mmHg at research visit or from the mean of BP measures during the home screening period, OR
- SBP 130-139 mmHg at research visit or from the mean of BP measures during the home screening period plus at least one comorbid condition as stated in AHA guidelines (cardiovascular disease, heart failure, stroke, atrial fibrillation, chronic kidney disease, kidney transplant, or diabetes)
- Ability to provide informed consent
- Willingness and ability to use a HBPM
- Willingness to complete the necessary data collection procedures, including transmission of BP measurements and permission for study staff to access EHR and/or PHR data.
Who cannot join
- 1. Does not meet inclusion criteria
Trial locations and contacts
2 sites in 1 country.
United States2 sites
Anchorage Native Primary Care Center
Anchorage, Alaska, 99508
Benteh Nuutah Valley Native Primary Care Center
Wasilla, Alaska, 99645
About this study
Official title: Home Blood Pressure Monitoring Intervention for Self-Management of High Blood Pressure Among Alaska Native People
"Blood Pressure: Improving Control among Alaska Native People" (BP-ICAN) that targets blood pressure control among Alaska Native and American Indian (AN/AI) people diagnosed with hypertension. Participants will include adults with a diagnosis of hypertension who have not achieved blood pressure control. Primary Care Center (PCC) provider teams and associated panels of Alaska Native or American Indian (ANAI) adults will be randomized into the control or intervention arm. The investigators will recruit up to 10 ANAI adults per PCC provider for a total of 324 participants. Intervention participants will receive a home blood pressure monitor (HBPM), upload personal home blood pressure values into a data mall, and be encouraged to communicate with providers and pharmacists about HBPM results using an online electronic health record application, telephone, or other existing clinical processes. HBPM measurements for each intervention arm participant will be provided to provider teams and integrated pharmacists. Control participants will receive care as usual. Data will be collected over a 12 month period. Participants will meet with investigators at time of consent (baseline), and 3, 6, and 12 months after baseline. At each visit, participants will have blood pressure measured using 3 methods (aneroid sphygmomanometer, automated Omron upper arm cuff device, and automated Omron wrist cuff device), complete surveys, and have height, weight, and arm circumference measured. In-person measures are omitted during the pandemic and only one method of blood pressure measurement is used (upper arm cuff device). Clinical and service utilization information will be electronically queried with participant consent. The investigators will examine whether participants in the intervention arm have better blood pressure control at the end of the 12 month period than participants in the control arm.
Read the detailed description
Background:
Cardiovascular disease (CVD) and stroke have become leading causes of mortality among ANAI people, who experience CVD disparities in incidence, risk factors, and mortality, especially for stroke, compared to the general population. From 1994-2003 stroke mortality in ANAIs was at least 25% higher than for Whites in Alaska. Over the same period, stroke mortality for ANAIs under age 45 increased 400%, but declined in Whites. In addition, the decline in age-adjusted CVD mortality observed in recent decades within the general population does not extend to ANAIs. Controlling hypertension is a pillar of prevention for CVD and stroke.
Although ANAIs were formerly thought to have a very low prevalence of stroke and CVD, more reliable newer data indicate high levels of hypertension and associated mortality. A recent systematic review of 141 publications on hypertension in ANAI people documented a significant increase in recorded prevalence over the past 3 decades, as well as a significantly higher prevalence in ANAI adults than in reference populations, usually White. Aggregated data from the Behavioral Risk Factor Surveillance System (BRFSS) also show a higher prevalence of self-reported hypertension in ANAIs than in non-Hispanic Whites (27% vs. 22%). The National Health Interview Survey found a similar disparity of 35% vs 26% in ANAIs vs. Whites. As in non-Hispanic Whites, 61% of ANAIs with hypertension were taking anti-hypertensive medication. In a previous study, an investigator on the present proposal examined the health records of 524 ANAI elders, finding that 23% had undiagnosed hypertension, and 38% had diagnosed hypertension. Of those with diagnoses, 81% were taking medication, 37% had well-controlled blood pressure (BP), and lifestyle counseling was rare.
Ongoing management of high BP often requires healthcare providers to initiate or intensify therapy in response to uncontrolled high BP. A recent review concluded that the patient/provider relationship, patient/provider communication, and patient-centered decision making were essential to appropriate decisions on medication change. Another study using electronic health record (EHR) data on military veterans found that ~60% of patients with hypertension had poorly controlled systolic BP, yet less than half of clinicians made medication changes after a computer-generated notification.
Improving BP control requires the involvement not only of individuals but of healthcare systems and social environments. Communications must extend care to patients "where patients are" outside the clinic; facilitate BP self-management; and minimize barriers to care AN/AIs face in healthcare access. Across Alaska, 60% of residents are medically underserved, and in 75% of Alaskan communities, regardless of residents' race, comprehensive healthcare services are accessible only by air or water. Even in urban areas, health disparities among AN/AIs persist, and access to care is affected by factors such as lack of transportation.
CVD morbidity, mortality, and organ damage are more accurately predicted by home blood pressure monitoring (HBPM) than by in-office measurements. HBPM avoids over-treating sporadic high BP readings and "white coat" hypertension while facilitating control of both resistant and "masked" hypertension (high at home and normal in the clinic), which are associated with stroke. Compared to usual care or HBPM alone, HBPM combined with self-titration of medications or with physician, pharmacist, or nurse management leads to better use of medications and BP control. Research shows the value of using HBPM values to trigger modifications in anti-hypertensive regimens, and the addition of provider feedback, patient and provider education, and decision-making support to encourage treatment adjustments improves control even more. HBPM can support patient decision making, provide data to providers, facilitate patient/provider communication, and engage, educate, and empower patients. HBPM devices are widely accepted by patients, who prefer them to clinic-based measurements. HBPM interventions appear to be most effective in patients with less well-controlled BP at baseline. Therefore, tailored HBPM interventions have been developed for minorities, who may receive more benefit from HBPM than Whites.
Significance:
BP-ICAN is innovative in many ways. First, it will be the only rigorous, population-based study about BP control for prevention of CVD and stroke in ANs, and one of very few multilevel interventions in any minority population. Second, the Southcentral Foundation (SCF) service area includes rural, suburban, and urban locations. Third, the intervention design addresses therapeutic inertia, a well-recognized barrier to hypertension control that is often neglected in clinical trials, so the approach to improve self-efficacy and ownership should lead to more timely communication with providers and titration of medications.
The investigators will conduct a group-randomized trial for improving BP control among ANAI adults with diagnosed hypertension. Study group assignment will occur by randomizing all SCF primary care panels to the BP-ICAN or usual care control arms; adults with uncontrolled hypertension will be nested within groups defined by panel, which corresponds to one provider. For each panel, investigators will recruit up to 10 ANAI adults (expecting average of 8-9 per provider, for a total n = 324) who have had systolic BP ≥ 130 mmHg measured at one or more clinic visits in the past 18 months OR who have previously diagnosed hypertension and systolic BP ≥ 130 mmHg measured at the study screening or home screening visit. The study period for all participants will last 12 months.
Participants who are randomized to the BP-ICAN arm will receive education about BP control, CVD and stroke and the importance of hypertension management for prevention, other lifestyle changes that can prevent or reduce morbidity from hypertension, and educational materials about the importance of timely response to uncontrolled hypertension. BP-ICAN arm participants will also receive HBPM equipment (Omron device) and training in its use, interpretation of results, and assistance with communicating high BP values to healthcare providers. Lastly, participants will receive culturally tailored text messages to reinforce the educational material and motivate adherence to HBPM and provider communication strategies. Participants whose providers have been randomized to the control condition will continue to receive care as usual.
Patient-initiated communication about uncontrolled BP will serve as one component of the provider-level intervention. Participants will be trained to sync HBPM and smart phone to automatically upload BP measurements into a data repository using Omron's free wellness application. This will update the participant's data on Omron's Wellness Application website. Investigators plan to use a cloud-based technology platform to serve as a data repository and are working with tribal leadership, institutional privacy officers, compliance officers, and providers on how data will displayed and stored within the health care system. The goal is to make aggregate BP measure data available to providers in either a personal health record (PHR) and/or health information exchange (HIE) that allows for transmission of select measures into the electronic health and or population health record. Note that this protocol was developed based on extensive collaboration with SCF providers.
At the individual level, the primary outcome is within-person change in systolic BP. Secondary outcomes are diastolic BP, anti-hypertensive medication use and adherence, physical activity, weight, and tobacco use. Individual-level outcomes will be measured at baseline, 3 months, 6 months, and 1 year post-baseline. At the provider level, the primary outcome is change in prescribing behavior for medication and other relevant lifestyle changes. At the systems level, the primary outcome is change in systolic BP for all adults with hypertension whose providers are randomized to the BP-ICAN arm vs. the care as usual arm, regardless of whether the adults were directly enrolled into the study.
- Conditions
- Hypertension
- Being tested
- BP-ICAN
- Keywords
- High Blood Pressure, Alaska Native and American Indian, Home Blood Pressure Monitoring, Self-efficacy, Primary Care
- Medical subject headings
- Hypertension
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BP-ICANDevice
One of two home blood pressure monitor devices will be used.
- Omron 7 Series Wrist cuff
- Omron 10 Series Upper Arm cuff
| Study group | Role | What they receive |
|---|---|---|
| BP-ICAN | Active comparator | Participants in the BP-ICAN arm will receive a home blood pressure monitor to be used twice daily for 12 months. Participants' home blood pressure measurements will be shared with their provider and participants will receive a series of text messages including topics on the importance of managing hypertension, reminders to measure blood pressure with their device, and motivational messages on diet and exercise. Receives: Device: BP-ICAN |
| Control | No intervention | Participants in the control arm will receive care as usual for the treatment of hypertension |
What is being measured
The primary outcome is the main question the study is designed to answer.
Individual-level: within-person change in systolic blood pressure
Examine change in systolic blood pressure (mmHg) between participants in the intervention group compared to the control group.
Measured: 12 months
Provider-level: frequency of antihypertensive medication adjustments
Examine number of medication adjustments (new prescription or change in dose of antihypertensive medications) between participants in the intervention group compared to the control group.
Measured: 3 months, 6 months, and 12 months
System-level: change in systolic blood pressure for all patients with hypertension
Examine change in systolic blood pressure (mmHg) between all patients whose providers are in the intervention group (receiving automated alerts about high blood pressure and pharmacist support), compared to patients whose providers are in the control group (do not receive alerts and pharmacist support).
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Mar 2019
- Study start19 Feb 2019
- Primary completion30 Sep 2022
- Study completion30 Sep 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (39)Papers the sponsor has linked to this study.
- Other trials for HypertensionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Group randomized comparison trial
- Masking
- None (open label)
- Enrolment
- 164 participants (actual)
Sponsor and investigators
- Lead sponsor
- Southcentral Foundation
- Sponsor type
- University, hospital or other
- Collaborators
- Washington State University
- Responsible party
- Principal investigator, Denise Dillard, Southcentral Foundation
- Investigators
- Denise A Dillard, PhD, Principal investigator, Southcentral Foundation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03872856
- Sponsor's protocol ID
- BP-ICAN-1U54MD011240-01
- Other IDs
- 2017-08-038
- Acronym
- CHAR2
- Status last verified
- Jul 2024
- First submitted
- 7 Mar 2019
- Last updated
- 1 Aug 2024
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Publications
Harris R, Nelson LA, Muller C, Buchwald D. Stroke in American Indians and Alaska Natives: A Systematic Review. Am J Public Health. 2015 Aug;105(8):e16-26. doi: 10.2105/AJPH.2015.302698. Epub 2015 Jun 11.
PubMed 26066955Hutchinson RN, Shin S. Systematic review of health disparities for cardiovascular diseases and associated factors among American Indian and Alaska Native populations. PLoS One. 2014 Jan 15;9(1):e80973. doi: 10.1371/journal.pone.0080973. eCollection 2014.
PubMed 24454685Jolly SE, Howard BV, Umans JG. Cardiovascular Disease Among Alaska Native Peoples. Curr Cardiovasc Risk Rep. 2013 Dec 1;7(6):10.1007/s12170-013-0362-5. doi: 10.1007/s12170-013-0362-5.
PubMed 24367710Howard BV, Devereux RB, Cole SA, Davidson M, Dyke B, Ebbesson SO, Epstein SE, Robinson DR, Jarvis B, Kaufman DJ, Laston S, MacCluer JW, Okin PM, Roman MJ, Romenesko T, Ruotolo G, Swenson M, Wenger CR, Williams-Blangero S, Zhu J, Saccheus C, Fabsitz RR, Robbins DC. A genetic and epidemiologic study of cardiovascular disease in Alaska natives (GOCADAN): design and methods. Int J Circumpolar Health. 2005 Jun;64(3):206-21. doi: 10.3402/ijch.v64i3.17985.
PubMed 16050315Horner RD, Day GM, Lanier AP, Provost EM, Hamel RD, Trimble BA. Stroke mortality among Alaska Native people. Am J Public Health. 2009 Nov;99(11):1996-2000. doi: 10.2105/AJPH.2008.148221. Epub 2009 Sep 17.
PubMed 19762671Trimble B, Morgenstern LB. Stroke in minorities. Neurol Clin. 2008 Nov;26(4):1177-90, xi. doi: 10.1016/j.ncl.2008.05.010.
PubMed 19026907Howard BV, Lee ET, Cowan LD, Devereux RB, Galloway JM, Go OT, Howard WJ, Rhoades ER, Robbins DC, Sievers ML, Welty TK. Rising tide of cardiovascular disease in American Indians. The Strong Heart Study. Circulation. 1999 May 11;99(18):2389-95. doi: 10.1161/01.cir.99.18.2389.
PubMed 10318659Foulds HJ, Warburton DE. The blood pressure and hypertension experience among North American Indigenous populations. J Hypertens. 2014 Apr;32(4):724-34. doi: 10.1097/HJH.0000000000000084.
PubMed 24609208Zhao G, Ford ES, Mokdad AH. Racial/ethnic variation in hypertension-related lifestyle behaviours among US women with self-reported hypertension. J Hum Hypertens. 2008 Sep;22(9):608-16. doi: 10.1038/jhh.2008.52. Epub 2008 May 22.
PubMed 18496555Barnes PM, Adams PF, Powell-Griner E. Health characteristics of the American Indian or Alaska Native adult population: United States, 2004-2008. Natl Health Stat Report. 2010 Mar 9;(20):1-22.
PubMed 20583451Rhoades DA, Buchwald D. Hypertension in older urban Native-American primary care patients. J Am Geriatr Soc. 2003 Jun;51(6):774-81. doi: 10.1046/j.1365-2389.2003.51261.x.
PubMed 12757563Rose AJ, Shimada SL, Rothendler JA, Reisman JI, Glassman PA, Berlowitz DR, Kressin NR. The accuracy of clinician perceptions of "usual" blood pressure control. J Gen Intern Med. 2008 Feb;23(2):180-3. doi: 10.1007/s11606-007-0464-1. Epub 2007 Nov 28.
PubMed 18043980Lebeau JP, Cadwallader JS, Aubin-Auger I, Mercier A, Pasquet T, Rusch E, Hendrickx K, Vermeire E. The concept and definition of therapeutic inertia in hypertension in primary care: a qualitative systematic review. BMC Fam Pract. 2014 Jul 2;15:130. doi: 10.1186/1471-2296-15-130.
PubMed 24989986Oakes JM. The (mis)estimation of neighborhood effects: causal inference for a practicable social epidemiology. Soc Sci Med. 2004 May;58(10):1929-52. doi: 10.1016/j.socscimed.2003.08.004.
PubMed 15020009Diez Roux AV. Complex systems thinking and current impasses in health disparities research. Am J Public Health. 2011 Sep;101(9):1627-34. doi: 10.2105/AJPH.2011.300149. Epub 2011 Jul 21.
PubMed 21778505
Study at a glance
From the registry record, last updated by the sponsor on 1 Aug 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Home Blood Pressure Monitoring Intervention for Self-Management of High Blood Pressure Among Alaska Native People
- ClinicalTrials.gov ID
- NCT03872856
- Acronym / sponsor ID
- CHAR2 / BP-ICAN-1U54MD011240-01
- Conditions
- Hypertension
- Keywords
- High Blood Pressure, Alaska Native and American Indian, Home Blood Pressure Monitoring, Self-efficacy, Primary Care
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 164 participants (actual)
- Lead sponsor
- Southcentral FoundationUniversity, hospital or other
- Collaborators
- Washington State University
- Study start
- 19 Feb 2019 (actual)
- Primary completion
- 30 Sep 2022 (actual)
- Study completion
- 30 Sep 2023 (actual)
- First posted
- 13 Mar 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
"Blood Pressure: Improving Control among Alaska Native People" (BP-ICAN) that targets blood pressure control among Alaska Native and American Indian (AN/AI) people diagnosed with hypertension. Participants will include adults with a diagnosis of hypertension who have not achieved blood pressure control. Primary Care Center (PCC) provider teams and associated panels of Alaska Native or American Indian (ANAI) adults will be randomized into the control or intervention arm. The investigators will recruit up to 10 ANAI adults per PCC provider for a total of 324 participants. Intervention participants will receive a home blood pressure monitor (HBPM), upload personal home blood pressure values into a data mall, and be encouraged to communicate with providers and pharmacists about HBPM results using an online electronic health record application, telephone, or other existing clinical processes. HBPM measurements for each intervention arm participant will be provided to provider teams and integrated pharmacists. Control participants will receive care as usual. Data will be collected over a 12 month period. Participants will meet with investigators at time of consent (baseline), and 3, 6, and 12 months after baseline. At each visit, participants will have blood pressure measured using 3 methods (aneroid sphygmomanometer, automated Omron upper arm cuff device, and automated Omron wrist cuff device), complete surveys, and have height, weight, and arm circumference measured. In-person measures are omitted during the pandemic and only one method of blood pressure measurement is used (upper arm cuff device). Clinical and service utilization information will be electronically queried with participant consent. The investigators will examine whether participants in the intervention arm have better blood pressure control at the end of the 12 month period than participants in the control arm.
Detailed description
Background:
Cardiovascular disease (CVD) and stroke have become leading causes of mortality among ANAI people, who experience CVD disparities in incidence, risk factors, and mortality, especially for stroke, compared to the general population. From 1994-2003 stroke mortality in ANAIs was at least 25% higher than for Whites in Alaska. Over the same period, stroke mortality for ANAIs under age 45 increased 400%, but declined in Whites. In addition, the decline in age-adjusted CVD mortality observed in recent decades within the general population does not extend to ANAIs. Controlling hypertension is a pillar of prevention for CVD and stroke.
Although ANAIs were formerly thought to have a very low prevalence of stroke and CVD, more reliable newer data indicate high levels of hypertension and associated mortality. A recent systematic review of 141 publications on hypertension in ANAI people documented a significant increase in recorded prevalence over the past 3 decades, as well as a significantly higher prevalence in ANAI adults than in reference populations, usually White. Aggregated data from the Behavioral Risk Factor Surveillance System (BRFSS) also show a higher prevalence of self-reported hypertension in ANAIs than in non-Hispanic Whites (27% vs. 22%). The National Health Interview Survey found a similar disparity of 35% vs 26% in ANAIs vs. Whites. As in non-Hispanic Whites, 61% of ANAIs with hypertension were taking anti-hypertensive medication. In a previous study, an investigator on the present proposal examined the health records of 524 ANAI elders, finding that 23% had undiagnosed hypertension, and 38% had diagnosed hypertension. Of those with diagnoses, 81% were taking medication, 37% had well-controlled blood pressure (BP), and lifestyle counseling was rare.
Ongoing management of high BP often requires healthcare providers to initiate or intensify therapy in response to uncontrolled high BP. A recent review concluded that the patient/provider relationship, patient/provider communication, and patient-centered decision making were essential to appropriate decisions on medication change. Another study using electronic health record (EHR) data on military veterans found that ~60% of patients with hypertension had poorly controlled systolic BP, yet less than half of clinicians made medication changes after a computer-generated notification.
Improving BP control requires the involvement not only of individuals but of healthcare systems and social environments. Communications must extend care to patients "where patients are" outside the clinic; facilitate BP self-management; and minimize barriers to care AN/AIs face in healthcare access. Across Alaska, 60% of residents are medically underserved, and in 75% of Alaskan communities, regardless of residents' race, comprehensive healthcare services are accessible only by air or water. Even in urban areas, health disparities among AN/AIs persist, and access to care is affected by factors such as lack of transportation.
CVD morbidity, mortality, and organ damage are more accurately predicted by home blood pressure monitoring (HBPM) than by in-office measurements. HBPM avoids over-treating sporadic high BP readings and "white coat" hypertension while facilitating control of both resistant and "masked" hypertension (high at home and normal in the clinic), which are associated with stroke. Compared to usual care or HBPM alone, HBPM combined with self-titration of medications or with physician, pharmacist, or nurse management leads to better use of medications and BP control. Research shows the value of using HBPM values to trigger modifications in anti-hypertensive regimens, and the addition of provider feedback, patient and provider education, and decision-making support to encourage treatment adjustments improves control even more. HBPM can support patient decision making, provide data to providers, facilitate patient/provider communication, and engage, educate, and empower patients. HBPM devices are widely accepted by patients, who prefer them to clinic-based measurements. HBPM interventions appear to be most effective in patients with less well-controlled BP at baseline. Therefore, tailored HBPM interventions have been developed for minorities, who may receive more benefit from HBPM than Whites.
Significance:
BP-ICAN is innovative in many ways. First, it will be the only rigorous, population-based study about BP control for prevention of CVD and stroke in ANs, and one of very few multilevel interventions in any minority population. Second, the Southcentral Foundation (SCF) service area includes rural, suburban, and urban locations. Third, the intervention design addresses therapeutic inertia, a well-recognized barrier to hypertension control that is often neglected in clinical trials, so the approach to improve self-efficacy and ownership should lead to more timely communication with providers and titration of medications.
The investigators will conduct a group-randomized trial for improving BP control among ANAI adults with diagnosed hypertension. Study group assignment will occur by randomizing all SCF primary care panels to the BP-ICAN or usual care control arms; adults with uncontrolled hypertension will be nested within groups defined by panel, which corresponds to one provider. For each panel, investigators will recruit up to 10 ANAI adults (expecting average of 8-9 per provider, for a total n = 324) who have had systolic BP ≥ 130 mmHg measured at one or more clinic visits in the past 18 months OR who have previously diagnosed hypertension and systolic BP ≥ 130 mmHg measured at the study screening or home screening visit. The study period for all participants will last 12 months.
Participants who are randomized to the BP-ICAN arm will receive education about BP control, CVD and stroke and the importance of hypertension management for prevention, other lifestyle changes that can prevent or reduce morbidity from hypertension, and educational materials about the importance of timely response to uncontrolled hypertension. BP-ICAN arm participants will also receive HBPM equipment (Omron device) and training in its use, interpretation of results, and assistance with communicating high BP values to healthcare providers. Lastly, participants will receive culturally tailored text messages to reinforce the educational material and motivate adherence to HBPM and provider communication strategies. Participants whose providers have been randomized to the control condition will continue to receive care as usual.
Patient-initiated communication about uncontrolled BP will serve as one component of the provider-level intervention. Participants will be trained to sync HBPM and smart phone to automatically upload BP measurements into a data repository using Omron's free wellness application. This will update the participant's data on Omron's Wellness Application website. Investigators plan to use a cloud-based technology platform to serve as a data repository and are working with tribal leadership, institutional privacy officers, compliance officers, and providers on how data will displayed and stored within the health care system. The goal is to make aggregate BP measure data available to providers in either a personal health record (PHR) and/or health information exchange (HIE) that allows for transmission of select measures into the electronic health and or population health record. Note that this protocol was developed based on extensive collaboration with SCF providers.
At the individual level, the primary outcome is within-person change in systolic BP. Secondary outcomes are diastolic BP, anti-hypertensive medication use and adherence, physical activity, weight, and tobacco use. Individual-level outcomes will be measured at baseline, 3 months, 6 months, and 1 year post-baseline. At the provider level, the primary outcome is change in prescribing behavior for medication and other relevant lifestyle changes. At the systems level, the primary outcome is change in systolic BP for all adults with hypertension whose providers are randomized to the BP-ICAN arm vs. the care as usual arm, regardless of whether the adults were directly enrolled into the study.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Group randomized comparison trial
| Arm | Type | Receives |
|---|---|---|
| BP-ICAN | Active comparator | Device: BP-ICANParticipants in the BP-ICAN arm will receive a home blood pressure monitor to be used twice daily for 12 months. Participants' home blood pressure measurements will be shared with their provider and participants will receive a series of text messages including topics on the importance of managing hypertension, reminders to measure blood pressure with their device, and motivational messages on diet and exercise. |
| Control | No intervention | –Participants in the control arm will receive care as usual for the treatment of hypertension |
Who may qualify
- Ages
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (13 listed)
- At least one visit to SCF providers or Community Health Aides within the previous year
- Alaska Native or American Indian
- At least 18 years old
- Meet one of the following two conditions:
- <!-- -->
Key exclusion criteria (1 listed)
- 1. Does not meet inclusion criteria
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BP-ICANOne of two home blood pressure monitor devices will be used. 1. Omron 7 Series Wrist cuff 2. Omron 10 Series Upper Arm cuff | Device | BP-ICAN |
Primary outcome
Individual-level: within-person change in systolic blood pressure
Time frame: 12 months
Examine change in systolic blood pressure (mmHg) between participants in the intervention group compared to the control group.
Provider-level: frequency of antihypertensive medication adjustments
Time frame: 3 months, 6 months, and 12 months
Examine number of medication adjustments (new prescription or change in dose of antihypertensive medications) between participants in the intervention group compared to the control group.
System-level: change in systolic blood pressure for all patients with hypertension
Time frame: 12 months
Examine change in systolic blood pressure (mmHg) between all patients whose providers are in the intervention group (receiving automated alerts about high blood pressure and pharmacist support), compared to patients whose providers are in the control group (do not receive alerts and pharmacist support).
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Aug 2024.
- Background: PubMed 26066955Harris R, Nelson LA, Muller C, Buchwald D. Stroke in American Indians and Alaska Natives: A Systematic Review. Am J Public Health. 2015 Aug;105(8):e16-26. doi: 10.2105/AJPH.2015.302698. Epub 2015 Jun 11.
- Background: PubMed 24454685Hutchinson RN, Shin S. Systematic review of health disparities for cardiovascular diseases and associated factors among American Indian and Alaska Native populations. PLoS One. 2014 Jan 15;9(1):e80973. doi: 10.1371/journal.pone.0080973. eCollection 2014.
- Background: PubMed 24367710Jolly SE, Howard BV, Umans JG. Cardiovascular Disease Among Alaska Native Peoples. Curr Cardiovasc Risk Rep. 2013 Dec 1;7(6):10.1007/s12170-013-0362-5. doi: 10.1007/s12170-013-0362-5.
- Background: PubMed 16050315Howard BV, Devereux RB, Cole SA, Davidson M, Dyke B, Ebbesson SO, Epstein SE, Robinson DR, Jarvis B, Kaufman DJ, Laston S, MacCluer JW, Okin PM, Roman MJ, Romenesko T, Ruotolo G, Swenson M, Wenger CR, Williams-Blangero S, Zhu J, Saccheus C, Fabsitz RR, Robbins DC. A genetic and epidemiologic study of cardiovascular disease in Alaska natives (GOCADAN): design and methods. Int J Circumpolar Health. 2005 Jun;64(3):206-21. doi: 10.3402/ijch.v64i3.17985.
- Background: PubMed 19762671Horner RD, Day GM, Lanier AP, Provost EM, Hamel RD, Trimble BA. Stroke mortality among Alaska Native people. Am J Public Health. 2009 Nov;99(11):1996-2000. doi: 10.2105/AJPH.2008.148221. Epub 2009 Sep 17.
- Background: PubMed 19026907Trimble B, Morgenstern LB. Stroke in minorities. Neurol Clin. 2008 Nov;26(4):1177-90, xi. doi: 10.1016/j.ncl.2008.05.010.
- Background: PubMed 10318659Howard BV, Lee ET, Cowan LD, Devereux RB, Galloway JM, Go OT, Howard WJ, Rhoades ER, Robbins DC, Sievers ML, Welty TK. Rising tide of cardiovascular disease in American Indians. The Strong Heart Study. Circulation. 1999 May 11;99(18):2389-95. doi: 10.1161/01.cir.99.18.2389.
- Background: PubMed 24609208Foulds HJ, Warburton DE. The blood pressure and hypertension experience among North American Indigenous populations. J Hypertens. 2014 Apr;32(4):724-34. doi: 10.1097/HJH.0000000000000084.
- Background: PubMed 18496555Zhao G, Ford ES, Mokdad AH. Racial/ethnic variation in hypertension-related lifestyle behaviours among US women with self-reported hypertension. J Hum Hypertens. 2008 Sep;22(9):608-16. doi: 10.1038/jhh.2008.52. Epub 2008 May 22.
- Background: PubMed 20583451Barnes PM, Adams PF, Powell-Griner E. Health characteristics of the American Indian or Alaska Native adult population: United States, 2004-2008. Natl Health Stat Report. 2010 Mar 9;(20):1-22.
- Background: PubMed 12757563Rhoades DA, Buchwald D. Hypertension in older urban Native-American primary care patients. J Am Geriatr Soc. 2003 Jun;51(6):774-81. doi: 10.1046/j.1365-2389.2003.51261.x.
- Background: PubMed 18043980Rose AJ, Shimada SL, Rothendler JA, Reisman JI, Glassman PA, Berlowitz DR, Kressin NR. The accuracy of clinician perceptions of "usual" blood pressure control. J Gen Intern Med. 2008 Feb;23(2):180-3. doi: 10.1007/s11606-007-0464-1. Epub 2007 Nov 28.
- Individual participant dataSharing planned: No
Related trials for Hypertension
Active, not recruiting
Digital Reinforcement of Motivational Interviewing Micro-Skills Among Primary Care Healthcare Professionals
Hypertension (Without Type 2 Diabetes Mellitus)
Recruiting
Investigating Vascular Properties of HEMI and SPG Signals in Individuals With or at Risk for Chronic Kidney Disease
Chronic Kidney Disease, Hypertension (HTN)
Recruiting
Trial Phase: Syndemic Adapted Medly Uganda
Mental Health
Not yet recruitingPhase 2/3
An Open-Label Extension Study to Evaluate Inhaled Treprostinil SMI in Participants With Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease (PH-COPD)
Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease
Enrolling by invitation
Testing Implementation Strategies to Support Clinic Fidelity to an Outpatient Hypertension Bundle
Pregnancy Related, Hypertension
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Denise A Dillard, PhD principal investigator
Southcentral Foundation
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing BP-ICAN in people with Hypertension, run by Southcentral Foundation at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 13 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Individual-level: within-person change in systolic blood pressure (time frame: 12 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03872856, which also lists 39 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Aug 2024.