Placebo Clinical Trial
— BEET_ELDERLYOfficial title:
Neuromuscular Responses to Acute Beetroot Ingestion in Women Older Adults. Performance and Side Effects
Verified date | May 2022 |
Source | Universidad Francisco de Vitoria |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Beetroot juice supplementation has shown the capacity for provoking different physiological effects (e.g. vasodilation and muscle contraction increments). However, the effects of beetroot juice ingestion on neuromuscular performance in women older adults are barely studied. In this randomized placebo-controlled study, we investigated the effects of beetroot acute supplementation in improving neuromuscular performance in women older adults
Status | Completed |
Enrollment | 9 |
Est. completion date | April 10, 2022 |
Est. primary completion date | March 18, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 65 Years to 80 Years |
Eligibility | Inclusion Criteria: - Women >65 or <85 years of age. - In good health, as determined by the investigator's review of history. Exclusion Criteria: (based in previous studies on this topic (doi: 10.1093/gerona/glaa311). Men and women <65 or >85 years of age Unable to provide informed consent Current smokers Significant orthopedic limitations or other contraindications to strenuous exercise Those taking proton pump inhibitors, antacids, xanthine oxidase inhibitors, or on hormone replacement therapy Those taking anti-coagulants or on anti-platelet therapy History of neuromuscular disease (e.g., cervical spondylotic radiculomyelpathy, lumbar spondylosis, amyotrophic lateral sclerosis, Guillain-Barré syndrome, and acquired demyelinating polyneuropathies) Cardiovascular disease (e.g., > stage I hypertension, heart failure, myocardial infarction/ischemia significant myocardial or pericardial diseases (e.g. amyloidosis, constriction), Moderate or severe valvular disease, renal disease, liver disease, or anemia |
Country | Name | City | State |
---|---|---|---|
Spain | Universidad Francisco de Vitoria | Pozuelo de Alarcón | Madrid |
Lead Sponsor | Collaborator |
---|---|
Universidad Francisco de Vitoria |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in maximal isometric handgrip strength (N) | Using a dynamometer and measuring dominant/ non-dominant side | 1-week | |
Primary | Changes in 6-m gait speed test | Using a photocell timing gates (seconds) | 1-week | |
Primary | Changes in Time Up and Go test | Using a photocell timing gates (seconds) | 1-week | |
Primary | Changes in Sit and Stand Test | Using Power Frail APP | 1-week | |
Primary | 6-Minute Walk Test | 1-week | ||
Secondary | Rate of perception effort (RPE) | Using a validated scale (1-10 points) | 1-week | |
Secondary | Side effects questionnarie | Using a side-effects questionnarie (YES/NO scale) | 1-week |
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