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| ID | Type | Description | Link |
|---|---|---|---|
| OCR26682 | Other Identifier | UF OnCore | |
| 5R21AG064282 | U.S. NIH Grant/Contract | View source | |
| AWD06755 | Other Identifier | UFIRST |
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| Name | Class |
|---|---|
| National Institute on Aging (NIA) | NIH |
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More than 80% of older adults have hypertension, with higher prevalence of high systolic blood pressure (SBP) putting them at high risk for cardiovascular (CV) disease and death. Novel compound, nicotinamide riboside may enhance the effects of exercise therapy in hypertensive older adults.
More than 80% of older adults have hypertension, with a higher prevalence of high systolic blood pressure (SBP) putting them at high risk for cardiovascular (CV) disease and death. Because drug therapy that lowers SBP is associated with side effects such as hypotension, syncope, and kidney dysfunction, there is a great need for effective lifestyle SBP-lowering interventions for the older population that can replace drug therapy. While aerobic exercise is a recommended lifestyle intervention for controlling SBP and preventing CV disease naturally, in older adults it has been shown to be less effective in vascular-tissue remodeling because of arterial stiffness, resulting in less efficient SBP control. Reduced bioavailability of nicotinamide adenine dinucleotide (NAD+), a cofactor for the deacetylase sirtuin1 (SIRT1), may contribute to age-related vascular dysfunction via oxidative stress and reduced nitric oxide (NO). Exercise-induced overexpression of NAD+-dependent SIRT1 improves the bioavailability of NO. Preclinical evidence suggests that poor vascular function improvement in response to exercise in older mice is caused by insufficient NAD+ levels to stimulate SIRT1 activity. Importantly, replenishment of NAD+ levels induced vascular remodeling, improved vascular function, and reduced SBP in mice. An objective of this study, therefore, is to test a combination of aerobic exercise and nicotinamide riboside, a compound that replenishes NAD+ levels, to optimize exercise's SBP-lowering effect in hypertensive older adults. Initial human clinical trials demonstrated that nicotinamide riboside supplementation (1,000 mg/day) was safe and showed a higher potential to reduce SBP and arterial stiffness in participants with elevated SBP. As we have preclinical evidence that combining NAD+ replenishment with exercise is an ideal strategy for improving vascular function, our central hypothesis is that the intervention of aerobic-exercise training combined with nicotinamide riboside supplementation will reduce SBP in hypertensive older adults more effectively than will exercise alone. We will enroll 54 participants ≥ 55 years and older into either: (1) 1,000 mg/day of nicotinamide riboside plus 3 days/week of supervised, center-based walking exercise (n=18), or (2) the same exercise program combined with placebo (n=18), or (3) 1,000 mg/day of nicotinamide riboside alone (n=18). All participants will undergo daytime continuous SBP at baseline, 3 weeks, and 6 weeks, and arterial-stiffness measurements by pulse-wave velocity at baseline and at 6 weeks. Elevated SBP will be determined as daytime average equal to or above 130 mmHg, measured by the 24-hour blood-pressure device. To our knowledge, this study will be the first attempt to enhance exercise therapy with nicotinamide riboside in hypertensive older adults. We believe that nicotinamide riboside is "the missing piece of the puzzle" in improving vascular remodeling and SBP management in older adults. Preliminary evidence from this pilot study may support a full-scale Phase III clinical trial in hypertensive older adults. The ultimate goal of this line of research is to find adjuvant strategies to improve the exercise's SBP-lowering effects in older adults.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NR plus Walking Exercise | Active Comparator | 1,000 mg/day of NR combined with three days/week of supervised, center-based walking exercise (n=18) |
|
| Walking Exercise plus Placebo | Active Comparator | 1,000 mg/day of Placebo combined with three days/week of supervised, center-based walking exercise (n=18) |
|
| NR Alone | Active Comparator | 1,000 mg/day of NR |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Walking Exercise | Behavioral | Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Daytime Systolic Blood Pressure | The primary outcome of this study is the change in average daytime systolic blood pressure. Systolic blood pressure was measured every 20 minutes (min) during the day (from 0700 to 2200 hours) at baseline and week 6 visits. Based on the American Heart Association guideline, we selected twenty valid daytime blood pressure recordings to calculate the average daytime value, then we calculated the mean differences between week 6 and baseline. | Baseline; Week 6 |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Arterial Stiffness | The measurement of aortic pulse-wave velocity (PWV), particularly between the carotid and femoral arteries (cfPWV), was conducted using the SphygmoCor XCEL system. Briefly, cfPWV was determined by recording pressure pulse waves at the carotid and femoral arteries using a high-fidelity micromanometer and calculating the distance between the recording sites divided by the time delay between the carotid and the femoral pulse waves. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Robert Mankowski, PhD | University of Florida | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UF Institute on Aging | Gainesville | Florida | 32611 | United States |
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Of 147 enrolled participants, 54 met the eligible criteria and were randomized to treatment.
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| ID | Title | Description |
|---|---|---|
| FG000 | NR Plus Walking Exercise | 1,000 mg/day of NR combined with three days/week of supervised, center-based walking exercise (n=18) Walking Exercise: Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. Nicotinamide Riboside (NR): Participants randomized to this intervention will receive 1,000 mg/day of NR. |
| FG001 | Walking Exercise Plus Placebo | 1,000 mg/day of Placebo combined with three days/week of supervised, center-based walking exercise (n=18) Walking Exercise: Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. |
| FG002 | NR Alone | 1,000 mg/day of NR Nicotinamide Riboside (NR): Participants randomized to this intervention will receive 1,000 mg/day of NR. |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | NR Plus Walking Exercise | 1,000 mg/day of NR combined with three days/week of supervised, center-based walking exercise (n=18) Walking Exercise: Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. Nicotinamide Riboside (NR): Participants randomized to this intervention will receive 1,000 mg/day of NR. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Change in Daytime Systolic Blood Pressure | The primary outcome of this study is the change in average daytime systolic blood pressure. Systolic blood pressure was measured every 20 minutes (min) during the day (from 0700 to 2200 hours) at baseline and week 6 visits. Based on the American Heart Association guideline, we selected twenty valid daytime blood pressure recordings to calculate the average daytime value, then we calculated the mean differences between week 6 and baseline. | Considering within-group differences for interested variables; we focus on the mean differences between week 6 and the baseline. | Posted | Mean | 95% Confidence Interval | mmHg | Baseline; Week 6 |
|
6 weeks
We collected adverse events at baseline, 3-week visits, 6-week visits, and every exercise session.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | NR Plus Walking Exercise | 1,000 mg/day of NR combined with three days/week of supervised, center-based walking exercise (n=18) Walking Exercise: Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. Nicotinamide Riboside (NR): Participants randomized to this intervention will receive 1,000 mg/day of NR. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Sepsis and Pneumonia | Infections and infestations | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Pancytopenia Worsening | Blood and lymphatic system disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Robert Mankowski | University of Florida | 352-294-5055 | r.mankowski@ufl.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 9, 2023 | Feb 17, 2024 | Prot_SAP_000.pdf |
| ICF | No | No | Yes | Informed Consent Form | Mar 2, 2023 | Apr 11, 2024 | ICF_001.pdf |
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| D004194 | Disease |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| C018613 | nicotinamide-beta-riboside |
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| Nicotinamide Riboside (NR) | Drug | Participants randomized to this intervention will receive 1,000 mg/day of NR. |
|
| Baseline; Week 6 |
| Adverse Event |
|
| BG001 |
| Walking Exercise Plus Placebo |
1,000 mg/day of Placebo combined with three days/week of supervised, center-based walking exercise (n=18) Walking Exercise: Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. |
| BG002 | NR Alone | 1,000 mg/day of NR Nicotinamide Riboside (NR): Participants randomized to this intervention will receive 1,000 mg/day of NR. |
| BG003 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Count of Participants | Participants |
|
| Body Mass Index | Mean | Standard Deviation | kg/m^2 |
|
| Baseline average daytime systolic blood pressure | Blood pressure was measured every 20 minutes (min) during the day (from 0700 to 2200 hours) at the baseline visit. Average daytime systolic blood pressure was calculated based on all the available daytime blood pressure readings recorded by the ambulatory blood pressure monitor. | Average daytime systolic blood pressure was calculated based on all the available daytime blood pressure readings recorded by the 24-hour ambulatory blood pressure monitor. | Mean | Standard Deviation | mmHg |
|
| Baseline average daytime diastolic blood pressure | Blood pressure was measured every 20 minutes (min) during the day (from 0700 to 2200 hours) at the baseline visit. Average daytime diastolic blood pressure was calculated based on all the available daytime blood pressure readings recorded by the ambulatory blood pressure monitor. | Average daytime diastolic blood pressure was calculated based on all the available daytime blood pressure readings recorded by the 24-hour ambulatory blood pressure monitor. | Mean | Standard Deviation | mmHg |
|
| OG001 | Walking Exercise Plus Placebo | 1,000 mg/day of Placebo combined with three days/week of supervised, center-based walking exercise (n=18) Walking Exercise: Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. |
| OG002 | NR Alone | 1,000 mg/day of NR Nicotinamide Riboside (NR): Participants randomized to this intervention will receive 1,000 mg/day of NR. |
|
|
| Secondary | Change in Arterial Stiffness | The measurement of aortic pulse-wave velocity (PWV), particularly between the carotid and femoral arteries (cfPWV), was conducted using the SphygmoCor XCEL system. Briefly, cfPWV was determined by recording pressure pulse waves at the carotid and femoral arteries using a high-fidelity micromanometer and calculating the distance between the recording sites divided by the time delay between the carotid and the femoral pulse waves. | Considering within-group differences for interested variables; we focus on the mean differences between week 6 and the baseline. | Posted | Mean | 95% Confidence Interval | m/s | Baseline; Week 6 |
|
|
|
| 0 |
| 17 |
| 0 |
| 17 |
| 9 |
| 17 |
| EG001 | Walking Exercise Plus Placebo | 1,000 mg/day of Placebo combined with three days/week of supervised, center-based walking exercise (n=18) Walking Exercise: Participants randomized to this intervention 3 days/week of supervised, center-based walking exercise. | 0 | 18 | 0 | 18 | 12 | 18 |
| EG002 | NR Alone | 1,000 mg/day of NR Nicotinamide Riboside (NR): Participants randomized to this intervention will receive 1,000 mg/day of NR. | 0 | 19 | 1 | 19 | 7 | 19 |
| Felt "spasm" feeling in the stomach | Gastrointestinal disorders | Systematic Assessment |
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| Headaches, loose stool, dry mouth and nose, fatigue | General disorders | Systematic Assessment |
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| High blood sugar | Metabolism and nutrition disorders | Systematic Assessment |
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| High PSA , high creatinine, frequent urination, increased hunger | General disorders | Systematic Assessment |
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| Sciatic Nerve Pain | Nervous system disorders | Systematic Assessment |
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| Knee Pain | Musculoskeletal and connective tissue disorders | Systematic Assessment |
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| Hurt Foot/Leg at Home | Musculoskeletal and connective tissue disorders | Systematic Assessment |
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| Soreness from Exercise | Musculoskeletal and connective tissue disorders | Systematic Assessment |
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| Symptoms (difficulty breathing, headache, etc.) due to COVID-19 | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
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| Allergies Became Worse | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
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| Tripped and fell | Musculoskeletal and connective tissue disorders | Systematic Assessment |
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| Cold or flu with symptoms (sneezing, runny nose, congestion, etc.) | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
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| Irregular Heartbeat | Cardiac disorders | Systematic Assessment |
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| Change in diabetes symptoms | Metabolism and nutrition disorders | Systematic Assessment |
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| UTI | Infections and infestations | Systematic Assessment |
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| Cyst removal | Surgical and medical procedures | Systematic Assessment |
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| Itching | Skin and subcutaneous tissue disorders | Systematic Assessment |
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| Bloody Urine | Renal and urinary disorders | Systematic Assessment |
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| Dizziness | General disorders | Systematic Assessment |
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| Sinus problems | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
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| Upper back pain | Musculoskeletal and connective tissue disorders | Systematic Assessment |
|
| Annoying feeling at the bottom of both feet due to calluses | Skin and subcutaneous tissue disorders | Systematic Assessment |
|
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