rrAD: Risk Reduction for Alzheimer's Disease

Sponsor

University of Texas Southwestern Medical Center (Other)

Overall Status

Completed

CT.gov ID

NCT02913664

Collaborator

Texas Health Resources (Other), University of Kansas Medical Center (Other), Washington University School of Medicine (Other), Pennington Biomedical Research Center (Other), Michigan State University (Other)

513

Enrollment

Locations

Arms

59.9

Actual Duration (Months)

128.3

Patients Per Site

2.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Physical inactivity, high blood pressure and dyslipidemia are risk factors for Alzheimer's disease (AD) and vascular dementia. Importantly, these risk factors are modifiable with lifestyle changes, pharmacological treatment, or both. The rrAD study will determine effects of aerobic exercise training and intensive vascular risk reduction on cognitive performance in older adults who have high risk for AD.

Condition or Disease	Intervention/Treatment	Phase
Cognitively Normal Older Adults Hypertension Subjective Cognitive Decline Family History of Alzheimer's Disease	Drug: Angiotensin II receptor blocker (ARB, losartan) and calcium channel blocker (CCB, amlodipine) Behavioral: Aerobic Exercise Training Other: Usual Care Behavioral: Stretching Exercise	Phase 2/Phase 3

Detailed Description

Numerous lines of evidence suggest that interventions that confer therapeutic benefits for cardiovascular health are also associated with improvements in, or preservation of, cognitive function. Many believe "What's good for the heart is good for the brain." However, stronge scientific evidence is needed to prove this hypothesis. The rrAD study is a 4-arm, multicenter, randomized trial to assess the effects of aerobic exercise training and intensive pharmacological reduction of vascular risk factors on cognitive performance in older adults who have high risk for AD, that is, those who have high blood pressure, family history of dementia or subjective memory complaints. Furthermore, rrAD will examine effects of exercise and vascular risk reduction on brain volume, perfusion, and neural network connectivity using magnetic resonance imaging (MRI).

Study Design

Study Type:

Interventional

Actual Enrollment :

513 participants

Allocation:

Randomized

Intervention Model:

Factorial Assignment

Masking:

Single (Outcomes Assessor)

Primary Purpose:

Prevention

Official Title:

Exercise and Intensive Vascular Risk Reduction in Preventing Dementia

Actual Study Start Date :

Feb 2, 2017

Actual Primary Completion Date :

Nov 30, 2021

Actual Study Completion Date :

Jan 31, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Aerobic Exercise (Ex) Aerobic exercise training; blood and cholesterol management will be standard-care by participant's regular doctor.	Behavioral: Aerobic Exercise Training Participants will take part in a supervised, moderate to vigorous aerobic exercise training program for approximately 24 months. This program consists of exercising 3 times per week for about 30 minutes per session at the beginning, and will increase to 4-5 times per week, 40-50 minutes per session over a period of 4-5 months. Exercise frequency, intensity and duration will be maintained at this level during the rest of the study period. Other: Usual Care Participants will follow their regular doctor's recommendations for blood pressure and lipid control.
Experimental: Intensive Reduction of Vascular Risk Factors (IRVR) Lowering SBP < 130 mmHg, administration of atorvastatin 80 mg daily, and stretching exercise.	Drug: Angiotensin II receptor blocker (ARB, losartan) and calcium channel blocker (CCB, amlodipine) Angiotensin II receptor blocker (ARB, losartan) and calcium channel blocker (CCB, amlodipine) will be used to reduce SBP<130 mmHg; atorvastatin 80 mg daily will be administered to reduce blood lipid level. Additional antihypertensives may be used if needed. Intensive Reduction of Vascular Risk Factors (IRVR) Behavioral: Stretching Exercise Participants will perform home-based stretching exercise 3 times per week, gradually increased to 4-5 times per week over a period of 4-5 months, and maintained at this level during the rest of the study period. They will be encouraged to attend monthly stretching exercise classes, which will be led by study staff or exercise trainers.
Experimental: IRVR+Ex A combination of IRVR and aerobic exercise training.	Drug: Angiotensin II receptor blocker (ARB, losartan) and calcium channel blocker (CCB, amlodipine) Angiotensin II receptor blocker (ARB, losartan) and calcium channel blocker (CCB, amlodipine) will be used to reduce SBP<130 mmHg; atorvastatin 80 mg daily will be administered to reduce blood lipid level. Additional antihypertensives may be used if needed. Intensive Reduction of Vascular Risk Factors (IRVR) Behavioral: Aerobic Exercise Training Participants will take part in a supervised, moderate to vigorous aerobic exercise training program for approximately 24 months. This program consists of exercising 3 times per week for about 30 minutes per session at the beginning, and will increase to 4-5 times per week, 40-50 minutes per session over a period of 4-5 months. Exercise frequency, intensity and duration will be maintained at this level during the rest of the study period.
Placebo Comparator: Usual Care Blood and cholesterol management will be standard-care by participant's regular doctor, and stretching exercise.	Other: Usual Care Participants will follow their regular doctor's recommendations for blood pressure and lipid control. Behavioral: Stretching Exercise Participants will perform home-based stretching exercise 3 times per week, gradually increased to 4-5 times per week over a period of 4-5 months, and maintained at this level during the rest of the study period. They will be encouraged to attend monthly stretching exercise classes, which will be led by study staff or exercise trainers.

Outcome Measures

Primary Outcome Measures

Change in global neurocognitive function [2 Years]
Alzheimer's Disease Cooperative Study-Preclinical Alzheimer Cognitive Composite (ADCS-PACC) and NIH Toolbox (NIH-TB) Cognition Battery will be used to assess changes in neurocognitive function. The composite z-score for global cognition will be obtained by conversion of individual test scores to the standardized z-scores, then averaged to obtain a composite score.

Secondary Outcome Measures

Domain-specific neurocognitive function assessed by using the tests included in the ADCS-PACC and NIH-TB Cognition. [2 Years]
Whole brain and hippocampal volume assessed via Magnetic Resonance Imaging (MRI). [2 years]
Global and regional brain perfusion assessed via Magnetic Resonance Imaging (MRI). [2 years]
Brain white matter hyperintensity (WMH) assessed via Magnetic Resonance Imaging (MRI). [2 years]
Brain white matter microstructural integrity assessed via Magnetic Resonance Imaging (MRI). [2 years]
Brain neural network functional connectivity assessed via functional Magnetic Resonance Imaging (MRI). [2 years]
Patient-reported outcomes (PRO) of mental and physical health and health-related quality of life assessed by using NIH PROMIS. [2 years]
Physical function assessed via the Short Physical Performance Battery (SPPB). [2 years]
Dual task performance assessed via distracted and non-distracted 10 meter walk. [2 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:

60 Years to 85 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Age 60-85, all races/ethnicities, and both sexes are eligible.
1. A positive family history of dementia defined as having at least one first-degree relative with a history of AD or other type of dementia,or b) having subjective cognitive decline.
Mini-Mental State Exam (MMSE) ≥ 26 to exclude gross dementia.
Must lead a sedentary lifestyle defined by not having an "active" rating on Rapid Assessment of Physical Activity (RAPA), i.e., score below 6 on RAPA.
1. Individuals treated for HTN with 110 ≤ SBP ≤ 130 mmHg; or b) Individuals with SBP > 130 and SBP < 180 (If an individual, not treated for HTN, has a SBP ≥ 125 mmHg, consider rescreening after 24 hours).
Willingness to be randomized into the treatment groups and ability to return to clinic for follow-up visits over 24 months.
Fluency in English, adequate visual and auditory acuity to allow neuropsychological testing.
Participants must have a regular healthcare provider.
Physical ability to undergo exercise training; able to walk 10 minutes without pain.

Exclusion Criteria:

Clinically documented history of stroke, focal neurological signs or other major cerebrovascular diseases based on clinical judgment or MRI/CT scans such as evidence of infection, infarction or other brain lesions.
Diagnosis of AD or other type of dementia, or significant neurologic diseases such as Parkinson's disease, seizure disorder, multiple sclerosis, history of severe head trauma or normal pressure hydrocephalus.
Evidence of severe major depression (GDS > 12, may be rescreened after 12 weeks or longer if evidence of reactive depression or temporary mood disturbances) or clinically significant psychopathology(e.g. psychosis and schizophrenia); if hospitalized in past year, can be rescreened in 6 months; or presence of a major psychiatric disorder that in the investigator's opinion, could interfere with adherence to research assessments or procedures.
Unstable heart disease based on clinical judgment (e.g., heart attack/cardiac arrest, cardiac bypass procedures within previous 6 months and congestive heart failure),or other severe medical conditions.
History of atrial fibrillation and evidence on ECG with any of the following: active symptoms of persistent palpitation, dizziness, history of syncope, chest pain, dyspnea, orthopnea, shortness of breath at rest, or paroxysmal nocturnal dyspnea within the past 6 months; resting heart rate of < 30 or > 110 bpm; taking class I or III anti-arrhythmic drugs including flecanide, propafenone, dronedarone, sotalol, dofetilide, and amiodarone; or clinical concerns for safely participating in exercise and lowering blood pressure.
Systolic BP equal or greater than 180 mmHg and/or diastolic BP equal or greater than 110 mmHg, may be rescreened in 1 week.
Orthostatic hypotension, defined as the third standing SBP < 100mmHg, may be rescreened after 2 weeks.
History of significant autoimmune disorders such as systemic lupus erythematosus, rheumatoid arthritis, or polymyalgia rheumatic.
Significant history of alcoholism or drug abuse within the last five years.
Uncontrolled diabetes mellitus, defined as hemoglobin A1C > 7.5%, or requiring insulin treatment.
Regularly smoking cigarette within the past year.
Women with a potential for pregnancy, lactation/child bearing (2 year post- menopausal or surgically sterile to be considered not child bearing potential).
Participant enrolled in another investigational drug or device study, either currently or within the past 2 months.
Severe obesity with BMI ≥ 45; clinical judgment should be applied in all cases to assess patient safety and anticipated compliance.
Allergy to angiotensin receptor blockers (ARBs), i.e., drugs that have a suffix "-sartan".
Allergy to other study drugs or their ingredients; for example, clinical history or self-reported allergy or intolerance to atorvastatin.
Abnormal screening laboratory tests (e.g., liver ALT and AST > 3 x ULN, CK > 3 x ULN, GFR < 30 or Hct < 28%); may be rescreened after 2 weeks or longer.
A medical condition likely to limit survival to less than 3 years.
Participant has any condition(s) judged by the study investigator to be medically inappropriate, risky or likely to cause poor study compliance. For example:
Plans to move outside the clinic catchment area in the next 2 years;
Significant concerns about participation in the study from spouse, significant other, or family members;
Lack of support from primary health care provider;
Residence too far from the study clinic site such that transportation is a barrier including persons who require transportation assistance provided by the study clinic funds for screening or randomization visits;
Residence in a nursing home; persons residing in an assisted living or retirement community are eligible if they meet the other criteria.
Other medical, psychiatric, or behavioral factors that, in the judgment of the site PI or clinician, may interfere with study participation or the ability to follow the study Protocol.
Couples or significant partners who live together cannot be enrolled or participate simultaneously in the study.
Lack of approval from participant's regular healthcare providers, i.e. a signed letter of agreement for the participants to be enrolled in rrAD.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University of Kansas Medical Center Research Institute	Kansas City	Kansas	United States	66160
2	Pennington Biomedical Research Center	Baton Rouge	Louisiana	United States	70808
3	Washington University in St. Louis	Saint Louis	Missouri	United States	63110
4	UT Southwestern Medical Center	Dallas	Texas	United States	75390

Sponsors and Collaborators

University of Texas Southwestern Medical Center
Texas Health Resources
University of Kansas Medical Center
Washington University School of Medicine
Pennington Biomedical Research Center
Michigan State University

Investigators

Principal Investigator: Rong Zhang, PhD, UT Southwestern Medical Center
Principal Investigator: Jeffrey Keller, PhD, Pennington Biomedical Research Center
Principal Investigator: Jeffrey Burns, MD, University of Kansas Medical Center
Principal Investigator: Ellen Binder, MD, Washington University School of Medicine
Principal Investigator: Munro Cullum, PhD, UT Southwestern
Principal Investigator: Diana Kerwin, MD, Texas Health Resources