The Effects of Almond Consumption on Functional Performance and Activity in Overweight Active Older Adults
NCT ID: NCT04778371
Last Updated: 2025-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
50 participants
INTERVENTIONAL
2021-03-02
2026-05-01
Brief Summary
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Detailed Description
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For this study, fifty men and postmenopausal women will follow a randomized-controlled crossover design. If individuals qualify for participation after the screening visit, they will be asked to complete a 3-day food record and wear an ActiGraph to track physical activity and sleeping patterns for the next seven days, to be returned at their Baseline Study Visit #1. During the Baseline Study Visit #1 assessments of: RMR, body composition (DXA), vascular assessments (FMD, PWV, PWA, blood pressure), heart rate, anthropometrics (height, weight, and waist/hip circumference), venous blood draw, POMS, and sleep quality (PSQI) will be collected. The following day, participants will return for their Baseline Physical Performance Visit #1 to complete assessments of submaximal aerobic capacity and the CS-PFP. Following this visit, participants will be provided with 12 weeks of almonds or the isocaloric snack. Participants will be asked to come in after 6 weeks to receive the rest of their dietary regimen and to monitor compliance. During week 11, participants will be asked to come to the study site to be given a 3-day food record and the ActiGraph to be retuned at the Post-Test Study Visit #1. After 12 weeks, participants will return to FSU to complete their Post-Test Study Visit #1, which will involve all the same assessments from the baseline study visit, as well as their Post-Test Physical Performance Visit #1, the next day. After the 4-week washout period, participants will similarly be asked to complete a 3-day food record and wear an ActiGraph for the following 7 days, to be returned upon the participants' Baseline Study Visit #2, where participants will crossover into receiving the corresponding dietary regimen and will follow the same procedures for the following 12 weeks.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
OTHER
NONE
Study Groups
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Almond supplement
Participants will consume 32 g dry roasted, unsalted almonds twice a day for 12 weeks
Almonds
64 g total dry roasted, unsalted almonds per day for a total of 12 weeks
Placebo matched supplement
Participants will consume 100 g granola bar, calorie matched to Almond, twice a day for 12 weeks
Placebo
200 g total calorie matched granola bar per day for total of 12 weeks
Interventions
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Almonds
64 g total dry roasted, unsalted almonds per day for a total of 12 weeks
Placebo
200 g total calorie matched granola bar per day for total of 12 weeks
Eligibility Criteria
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Inclusion Criteria
* Between the ages of 50-59 years
* Free of any chronic diseases such as cancer
* Active lifestyle (\>30 minutes, 3 days/week)
* BMI of 25.0 kg/m2 to 29.9 kg/m2 will be included
* There will be no restrictions based on race, ethnicity, or socioeconomic status.
Exclusion Criteria
* Uncontrolled hypertension (≥160/100 mmHg)
* BMI \<25.0 kg/m2 or \>29.9 kg/m2
* Other active chronic diseases such as cancer, asthma, glaucoma, kidney, liver and pancreatic disease
* Those who are not post-menopausal or on hormone replacement therapy
* Taking more than one anti-hypertensive or have been taking them for less than 3 months -Any musculoskeletal or orthopedic problem that would otherwise prevent completing the study Participants participating in a weight loss program or having lost or gain ≥10% bodyweight within the last 6 months
* Currently using tobacco
* Consumption of \>12 alcoholic drinks/week
* Nut allergies
* Frequent tree nut consumers (\>2 servings/week)
* In concurrent participation with another investigational study
* Currently consuming any performance supplement (i.e. creatine, nitric oxide, whey/casein protein, branched chain amino acids).
50 Years
59 Years
ALL
Yes
Sponsors
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Almond Board of California
OTHER
Florida State University
OTHER
Responsible Party
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Bob Hickner
Principal Investigator
Principal Investigators
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Robert Hickner, PhD
Role: PRINCIPAL_INVESTIGATOR
Florida State University
Locations
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Florida State University
Tallahassee, Florida, United States
Countries
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Other Identifiers
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00001394
Identifier Type: -
Identifier Source: org_study_id
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