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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04787718
Other study ID # 59997A
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 15, 2020
Est. completion date May 3, 2022

Study information

Verified date May 2022
Source San Diego State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Investigators specific aims are to compare the effects of consuming daily snacks of raw, shelled, unsalted almonds (2.0 ounces) versus an isocaloric amount of another commonly consumed snack food (pretzels) on energy (vigor) perception and physical activity, exercise performance (VO2max and measures of strength), strength and power performance as well as muscle soreness recovery after strenuous eccentrically-biased exercise.


Description:

To accomplish these aims, investigators will examine whether regular consumption of almonds versus a common snack food over a period of 8 weeks impacts longer term metabolic, physiological and behavioral responses related to energy sensations and exercise capacity/performance.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date May 3, 2022
Est. primary completion date May 3, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 50 Years
Eligibility Inclusion Criteria: - 30-50 years old - BMI of 23-30 Exclusion Criteria: - smoking, - medications known to impact inflammation, - musculoskeletal limitations and - use of supplements within 1 month of participation that are known to impact antioxidant - use of supplements within 1 month of participation that are known to impact inflammatory status

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Almond
2.0 oz of raw, shelled, unsalted almonds
Control group
an isocaloric amount of unsalted pretzels

Locations

Country Name City State
United States San Diego State University San Diego California

Sponsors (1)

Lead Sponsor Collaborator
San Diego State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes from baseline in energy (vigor) perception Energy (vigor) perception will be assessed using POMS questionnaire At baseline , at 8 weeks
Primary Changes from baseline in exercise performance VO2max will be assessed for measuring exercise performance At baseline , at 8 weeks
Secondary Changes from baseline in strength and power performance strength and power performance by be measure by biodex At baseline, at 8 weeks
Secondary Changes from baseline in muscle soreness muscle soreness will be measured by DOMES questionnaire At baseline, at 8 weeks
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