The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC)
Primary Purpose
Cognitive Impairment, Hypertension, Aging
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
candesartan
lisinopril
hydrochlorothiazide
nifedipine, long acting
metoprolol, long-acting
Sponsored by

About this trial
This is an interventional treatment trial for Cognitive Impairment focused on measuring cognitive disorders, angiotensin receptor blockers
Eligibility Criteria
Inclusion Criteria:
- 60 years or older
- Hypertension
- Cognitive criteria: score either 10 or less out of 15 for the executive clock draw test 1 (CLOX1) or less than or equal to 1 standard deviation from the corresponding age specific mean on the immediate memory subtest
Exclusion Criteria:
- Intolerance to ACEI or ARB
- History of congestive heart failure
- History of diabetes mellitus
- History of stroke (less than 6 months)
Sites / Locations
- University of Southern California
- Hebrew SeniorLife
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Candesartan
Lisinopril
HCTZ
Arm Description
Angiotensin Receptor Blocker
Angiotensin-Converting Enzyme (ACE) Inhibitor
Hydrochlorothiazide (diuretic)
Outcomes
Primary Outcome Measures
Cognitive Assessment: Trail Making Test Part B
This test requires the connection of sequentially numbered circles (A), and the connection of circles marked by numbers and letters in alternating sequence (B). This test is considered a benchmark of executive function. The test score is the time required to complete the task in seconds.
Cognitive Assessment: Hopkins Verbal Learning- Immediate Recall
This is a 12-item list learning test in which individuals are presented three learning and recall trials followed by a delayed recall and 24 item recognition test. The HVLT-R has been identified as an ideal memory measure for elderly patients, and appropriate reliability and validity have been shown in older individuals. The test score is the number of correct answers in the delayed recall ( score range 0-12)
Cognitive Assessment: Forward Digit Span Test
This test consists of series of digits of increasing length, some of which are recited as presented, and some of which are to be recited in reversed order. The forward digit span score ranges from 0 (ie cannot repeat two digits) to 8 ( participant can repeat up to 8 digits)
Secondary Outcome Measures
Blood Pressure Outcome: Systolic BP
Blood pressure was measured as follows: the participant was in the sitting position, rested for 5 minutes, no caffeine or smoking 2 hours prior to measurement, using appropriate cuff size (covering 60% of upper arm length and 80% of arm circumference), correct cuff placement (1-2 inches above brachial pulse on bare arm), and the bell of the stethoscope. The systolic blood pressure was defined as the pressure corresponding to the first korotkoff sounds (K1) and the diastolic as the pressure corresponding to the last korotkoff sound (K5). Blood pressure was measured in both arms and recorded
Blood Flow Velocity, Sitting
This reports the change in the least square mean from baseline to 12 months, adjusted for age
Full Information
NCT ID
NCT00605072
First Posted
January 11, 2008
Last Updated
January 14, 2013
Sponsor
University of Southern California
Collaborators
National Institute on Aging (NIA), Hebrew SeniorLife
1. Study Identification
Unique Protocol Identification Number
NCT00605072
Brief Title
The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial
Acronym
AVEC
Official Title
The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
Collaborators
National Institute on Aging (NIA), Hebrew SeniorLife
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to examine the effects of blood pressure medications on cognition and blood flow in hypertensive elderly patients with cognitive impairment. The hypothesis is that treatment with an angiotensin receptor blocker (ARB) or an angiotensin-converting enzyme inhibitor (ACEI) will be associated with a slower rate of further cognitive decline, improved cerebral blood flow and its regulation, and preserved physical function as compared to treatment with a diuretic (HCTZ), independent of blood pressure level.
Detailed Description
There is mounting evidence that hypertension, which affects more than 65% of the US elderly population, accelerates cognitive decline and increases the risk of functional disability among older individuals. Hypertension is also associated with cerebral blood flow reduction and dysregulation which contribute to further cognitive and functional impairment. Drugs that inhibit angiotensin II (ACEI and ARB) are commonly used antihypertensives and may have a protective effect on cognitive function, cerebral blood flow and physical function compared to other antihypertensives such as hydrochlorothiazide (HCTZ).
A total of 100 individuals will be recruited for this pilot 3-arm randomized study to investigate the effects of: (i) 12 months treatment with candesartan (ARB) compared to hydrochlorothiazide (HCTZ) and (ii) 12 months treatment with lisinopril (ACEI) compared to HCTZ and (iii) to estimate the effect size difference between lisinopril and losartan on cognition, cerebral blood flow regulation, and functional measures in a sample of elderly hypertensive individuals with objective evidence of cognitive impairment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Impairment, Hypertension, Aging
Keywords
cognitive disorders, angiotensin receptor blockers
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
53 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Candesartan
Arm Type
Experimental
Arm Description
Angiotensin Receptor Blocker
Arm Title
Lisinopril
Arm Type
Experimental
Arm Description
Angiotensin-Converting Enzyme (ACE) Inhibitor
Arm Title
HCTZ
Arm Type
Active Comparator
Arm Description
Hydrochlorothiazide (diuretic)
Intervention Type
Drug
Intervention Name(s)
candesartan
Other Intervention Name(s)
Atacand
Intervention Description
orally 8 mg increased to 16 mg then 32 mg to achieve target blood pressure of 140/90, then daily for 12 months
Intervention Type
Drug
Intervention Name(s)
lisinopril
Other Intervention Name(s)
Prinivil
Intervention Description
orally 10 mg increased to 20 mg then 40 mg to achieve target blood pressure of 140/90, then daily for 12 months
Intervention Type
Drug
Intervention Name(s)
hydrochlorothiazide
Other Intervention Name(s)
HCTZ, multiple brand names
Intervention Description
orally 12.5 mg increased to 25 mg to achieve target blood pressure of 140/90, then daily for 12 months
Intervention Type
Drug
Intervention Name(s)
nifedipine, long acting
Other Intervention Name(s)
Procardia XL
Intervention Description
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 30 mg increased to 60 mg and 90 mg in 2 week increments
Intervention Type
Drug
Intervention Name(s)
metoprolol, long-acting
Other Intervention Name(s)
Lopressor, Toprol XL
Intervention Description
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 12.5 mg increased to 25 mg and 50 mg
Primary Outcome Measure Information:
Title
Cognitive Assessment: Trail Making Test Part B
Description
This test requires the connection of sequentially numbered circles (A), and the connection of circles marked by numbers and letters in alternating sequence (B). This test is considered a benchmark of executive function. The test score is the time required to complete the task in seconds.
Time Frame
Baseline-12 months
Title
Cognitive Assessment: Hopkins Verbal Learning- Immediate Recall
Description
This is a 12-item list learning test in which individuals are presented three learning and recall trials followed by a delayed recall and 24 item recognition test. The HVLT-R has been identified as an ideal memory measure for elderly patients, and appropriate reliability and validity have been shown in older individuals. The test score is the number of correct answers in the delayed recall ( score range 0-12)
Time Frame
Baseline-12 months
Title
Cognitive Assessment: Forward Digit Span Test
Description
This test consists of series of digits of increasing length, some of which are recited as presented, and some of which are to be recited in reversed order. The forward digit span score ranges from 0 (ie cannot repeat two digits) to 8 ( participant can repeat up to 8 digits)
Time Frame
Baseline-12 months
Secondary Outcome Measure Information:
Title
Blood Pressure Outcome: Systolic BP
Description
Blood pressure was measured as follows: the participant was in the sitting position, rested for 5 minutes, no caffeine or smoking 2 hours prior to measurement, using appropriate cuff size (covering 60% of upper arm length and 80% of arm circumference), correct cuff placement (1-2 inches above brachial pulse on bare arm), and the bell of the stethoscope. The systolic blood pressure was defined as the pressure corresponding to the first korotkoff sounds (K1) and the diastolic as the pressure corresponding to the last korotkoff sound (K5). Blood pressure was measured in both arms and recorded
Time Frame
Baseline-12 months
Title
Blood Flow Velocity, Sitting
Description
This reports the change in the least square mean from baseline to 12 months, adjusted for age
Time Frame
Baseline-12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
60 years or older
Hypertension
Cognitive criteria: score either 10 or less out of 15 for the executive clock draw test 1 (CLOX1) or less than or equal to 1 standard deviation from the corresponding age specific mean on the immediate memory subtest
Exclusion Criteria:
Intolerance to ACEI or ARB
History of congestive heart failure
History of diabetes mellitus
History of stroke (less than 6 months)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ihab Hajjar, MD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Hebrew SeniorLife
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02131
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
15655124
Citation
Lipsitz LA, Gagnon M, Vyas M, Iloputaife I, Kiely DK, Sorond F, Serrador J, Cheng DM, Babikian V, Cupples LA. Antihypertensive therapy increases cerebral blood flow and carotid distensibility in hypertensive elderly subjects. Hypertension. 2005 Feb;45(2):216-21. doi: 10.1161/01.HYP.0000153094.09615.11. Epub 2005 Jan 17.
Results Reference
background
PubMed Identifier
19922631
Citation
Hajjar I, Hart M, Milberg W, Novak V, Lipsitz L. The rationale and design of the antihypertensives and vascular, endothelial, and cognitive function (AVEC) trial in elderly hypertensives with early cognitive impairment: role of the renin angiotensin system inhibition. BMC Geriatr. 2009 Nov 18;9:48. doi: 10.1186/1471-2318-9-48.
Results Reference
background
PubMed Identifier
22412114
Citation
Hajjar I, Hart M, Chen YL, Mack W, Milberg W, Chui H, Lipsitz L. Effect of antihypertensive therapy on cognitive function in early executive cognitive impairment: a double-blind randomized clinical trial. Arch Intern Med. 2012 Mar 12;172(5):442-4. doi: 10.1001/archinternmed.2011.1391. No abstract available.
Results Reference
result
PubMed Identifier
23350899
Citation
Hajjar I, Hart M, Chen YL, Mack W, Novak V, C Chui H, Lipsitz L. Antihypertensive therapy and cerebral hemodynamics in executive mild cognitive impairment: results of a pilot randomized clinical trial. J Am Geriatr Soc. 2013 Feb;61(2):194-201. doi: 10.1111/jgs.12100. Epub 2013 Jan 25.
Results Reference
derived
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The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial
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