Muscular InjuryNCT04958018
Almond Supplementation and Exercise Recovery
A study testing Almonds and Snack bars in people with Muscular Injury, run by Appalachian State University at 1 site in United States.
Trial summary
The PURPOSE of this study is to see if eating almonds for four weeks will reduce muscle damage, soreness, and inflammation during several days of recovery from eccentric exercise. Read more about this study
- Who is it for?
- Ages 30 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Muscular Injury
- What is being tested?
- Almonds and Snack bars
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteUnited States
- Study dates
- 16 Jun 2021to 30 Oct 2021
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Male or female, ages 30-65 years.
- Non-smoker.
- Body mass index of 23 to 30 kg/m2.
- Not engaged in regular weight lifting (less than 3 sessions per week).
- Agree to train normally, maintain weight, and avoid the regular use of protein supplements, large-dose vitamin and mineral supplements, herbs, and medications that influence inflammation (especially Advil, Motrin, aspirin, and similar drugs) during the study.
- Categorized as "low risk" using a screening questionnaire.
- Generally healthy and without disease including heart disease, stroke, cancer, diabetes, arthritis.
- Willing to collect two 24-hour urine samples.
Who cannot join
- Inability to comply with study requirements.
- Engaged in regular weight training (3 or more times a week).
- Pregnant or breastfeeding.
- Any other condition that would interfere with successful completion of the study.
- Current diagnosis of heart disease, diabetes, or cancer (except for skin cancer).
- History of allergic reactions to almonds or cereal bars.
Trial locations and contacts
1 site in 1 country.
United States1 site
Appalachian State University Human Performance Lab, North Carolina Research Campus
Kannapolis, North Carolina, 28081
About this study
Official title: Influence of Almond Supplementation on Energy, Performance, and Inflammation Resolution From Exercise-Induced Muscle Damage
The PURPOSE of this study is to see if eating almonds for four weeks will reduce muscle damage, soreness, and inflammation during several days of recovery from eccentric exercise.
Read the detailed description
This will be the first study to determine if 4-weeks ingestion of nutrient-dense almonds improves feelings of energy and vitality, and mitigates post-exercise inflammation (plasma cytokine and oxylipin levels), muscle soreness, and muscle damage. An acute 90-minute bout of eccentric exercise will be used to induce muscle damage and inflammation in a group of 60 relatively untrained male and female adults (ages 30-65 years). Using a randomized, parallel group design, almond supplementation (57 g/d) for a 4-week period prior to the eccentric exercise challenge will be investigated as a countermeasure strategy to exercise-induced muscle damage and inflammation. The control group will ingest a calorie-matched common snack (cereal bars). To improve the potential for capturing an intervention effect, advanced mass spectrometry procedures will be utilized to measure changes in 70 different oxylipins and lipid mediators that are involved in regulating inflammation. C-reactive protein (CRP), six inflammatory cytokines, and muscle damage biomarkers will also be measured. Blood samples (7 total) will be collected before and after the 4-week supplementation period, and then daily during 5 days of recovery from the eccentric exercise bout. The Profile of Mood States (POMS) will be used to measure mood state and specific domains including vigor or activity, and fatigue or inertia. Exercise performance will be measured each time a blood sample is collected using a comprehensive battery that includes vertical jump, leg/back muscle strength, bench press muscle endurance, and anaerobic power (30-second Wingate test).
Participants will be randomized to the almond or typical snack (cereal bars) supplement groups. The parallel group design is being utilized in this study because of the "repeat exercise bout" effect (i.e., post-exercise muscle damage and inflammation are reduced when the same bout is repeated within days and weeks of the first bout). Participants will come to the lab at 7:00 am at the beginning of the 4-week supplementation period, and then Monday (eccentric exercise bout) and Tuesday through Friday (recovery) in an overnight fasted state. The 4-week supplementation period was based on practical issues related to the research design. A 4-week almond supplementation period was commonly used in prior studies and was sufficient to demonstrate favorable blood lipid changes relative to control conditions.
Seven blood samples will be collected and analyzed for various measures of muscle damage, oxylipins, and inflammation. After each of the blood draws, participants will complete the POMS (energy, vitality) and provide a muscle soreness rating (DOMS). Physical activity will be monitored during the entire study using the International Physical Activity Questionnaire (IPAQ). The IPAQ was developed to measure health-related physical activity (PA) in populations. The short version of the IPAQ has been tested extensively and is now used in many international studies.
Study participants will come to the performance lab for orientation to the testing procedures. This will include a review of the consent form, completion of basic questionnaires, and an introduction to the eccentric muscle exercise bout and the strength/power performance testing protocol (about 1.5 hours) (visit #1). This will be followed by another lab session for pre-study measurements and sample collection with subjects in an overnight fasted state (visit #2) (see description below). A 3-day food record will be collected during the end of the 4-week supplementation period to assess the background diet.
Study participants will have to agree to 5 other lab visits during a one-week period (all overnight fasted condition). These lab visits will start at 7:00 am on Monday, with morning visits at 7:00 am on Tuesday through Friday. At each of the 5 lab visits, study participants will come to the lab at 7:00 am not having consumed food or beverages (other than water) for at least the previous 9 hours, and having abstained from vigorous exercise for at least the previous 24-48 hours. The Monday session will take about 2.5 hours (7:00 to 9:30 am), and the Tuesday through Friday sessions will take about 30-45 minutes each. The total amount of time participants will be asked to volunteer for this study is about 8-9 hours at the performance lab.
Participants will be randomized to almond or snack groups, and provided a 4-weeks supply of supplements. Participants in the almond group will consume 57 g almonds each day in split doses (half in the morning, half in the afternoon). Participants in the snack group will ingest a matched calorie, common snack bar in split doses (324 calories/day, Nutri-Grain cereal bars, 120 kcal each).
The daily dose of almonds (57 g) and just under 3 Nutri-Grain cereal bars will provide a distinct difference in nutrient intake. A serving of 57 g of almonds has 324 calories with 12 g of protein, 28 g of fat (17 g from monounsaturated, 6.6 g from polyunsaturated, 2.6 g from saturated), 12 g of carbohydrates and 6.6 g of fiber, 160 mg total polyphenols, and significant amounts of vitamin E (96% RDA), magnesium, manganese, copper, and other minerals.
Baseline Testing (Visit #2) Participants will provide a blood sample using standard phlebotomy procedures. Participants will also provide a spot urine sample, with instructions to capture a mid-stream urine sample in a disposable urine cup. Spot urine samples provide valid metabolite data as indicators of dietary intake. Height, body weight, and body composition will be measured in a private section of the lab. Bioelectrical impedance (BIA) using the seca BIA scale will be used to assess body composition (i.e., the percent of body weight that is fat tissue) and body weight. Participants will remove shoes and socks and stand with bare feet on the seca scale for about 7-10 seconds while grasping side rails with your hands. Percent body fat will also be measured using the BodPod. Participants will sit inside the BodPod with a tight-fitting swim suit for about 10 minutes while body fat is calculated. The Profile of Mood States (POMS) will be administered. Delayed onset of muscle soreness (DOMS) will be assessed using a 1-10 scale.
Participants will perform some light exercises to warm up, followed by five muscle function tests: vertical jump, bench press, leg-back strength, 60-yard shuttle run test, and anaerobic power through the 30-second Wingate test.
- Vertical jump: Participants will first stand erect with the feet flat on the floor and reach as high as possible with both arms and hands (standing reach height). Participants will then squat down and jump as high as possible with one arm and hand, and tap the measuring device on the Vertec vertical jump apparatus (jump height). This will be repeated three times, with the best score recorded as the difference between the jump and standing reach heights.
- Bench press to exhaustion at 50%/75%: Participants will lie down supine on a bench, and with spotters standing on either side attempt to bench press a weighted bar equal to 75% (males) or 50% (females) body weight as many times as possible (to a metronome set at 60 beats/min or 30 lifts/min). The bar must touch a foam block on the chest lightly in the down position, and the arms must be straight in the up position.
- Leg-Back Strength: Leg/lower back strength will be assessed with a dynamometer. With the legs slightly bent at the knee, participants will grasp a bar attached via a chain and a force measuring device with straight arms, and then lift up with maximal effort for several seconds. This will measure the isometric strength of both legs and back, and will be repeated three times.
- 30-Second Wingate Cycling Test, Anaerobic Power: The Lode cycle ergometer will be adjusted to the participant's body weight (7 watts per kilogram). After a warm up, participants will sprint cycle at maximal speed for 30 seconds. The peak power and average power will be recorded and adjusted to body weight.
- 60-Yard Shuttle Run Test: The shuttle run is a test of anaerobic speed endurance and agility, in which participants run to 5 yards, 10 yards, 15 yards, there and back, for a total of 60 yards. This is a ladder shuttle of progressing distances. Four marker cones are placed 5 yards apart. The participant starts from one end, runs 5 yards and back to the start, 10 yards and back, then 15 yards and finishes at the start line. A total of 60 yards is completed. The participant is required to touch the line with their hand at each turn, and runs through the finish line, for a total of five touches. The time to complete the test in seconds is recorded. The score is the best time of three trials.
Testing Sequence, Day of Eccentric Muscle Exercise (Monday) and 4-Days Recovery (Tuesday through Friday):
Participants will come to the lab at 7:00 am in an overnight fasted state (i.e., no food or beverages other than water for at least the previous 9 hours). Participants (on Monday only) will provide a spot urine sample that will be aliquoted, stored in a -80°C freezer, and then sent to Metabolon (Durham, NC) for global metabolomics analysis (to capture metabolite shifts related to almond ingestion). Participants will provide a blood sample, fill in the POMS, and give a DOMS rating. The almond or snack supplements (half dose) will be consumed. Participants will perform some light exercises to warm up, followed by five muscle function tests (same as baseline): vertical jump, bench press, leg-back strength, 60-yard shuttle run test, and anaerobic power through the 30-second Wingate test. Participants will take these performance tests before and after the 90-minute eccentric muscle exercise bout, and each of the following four mornings at the performance lab.
After taking the five performance tests, participants will engage in 90-minutes of eccentric exercise. This protocol induces significant muscle damage and soreness.
Immediately following exercise, participants will provide a muscle soreness rating and a blood sample. Participants will then take the five muscle function tests. Participants will ingest the supplements (half-dose) during the afternoon. Participants will return at 7:00 am in an overnight fasted state four days in a row (Tuesday through Friday) after Monday's eccentric exercise bout, and provide muscle soreness ratings and blood samples followed by ingestion of the supplements (half dose). Following ingestion of the supplements, participants will take the five muscle function tests. Participants will the second half dose of the supplements in the afternoon (Tuesday, Wednesday, Thursday). On Friday morning, participants will take the supplement (half dose) prior to the muscle function tests. During this week of testing, participants will engage in normal training.
The blood and urine samples will be analyzed for a panel of oxylipins, CRP and six cytokines, three muscle damage markers (creatine kinase, myoglobin, LDH), and urine metabolites.
- Conditions
- Muscular Injury
- Being tested
- Almonds, Snack bars
- Keywords
- almonds, exercise, inflammation, oxylipins, cytokines
- Medical subject headings
- Motor Activity, Inflammation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AlmondsDietary supplement
almond (Prunus dulcis) consumption
Snack barsDietary supplement
324 calories/day, Nutri-Grain cereal bars, 120 kcal each
| Study group | Role | What they receive |
|---|---|---|
| Almond | Experimental | 57 g almonds each day in split doses (half in the morning, half in the afternoon) Receives: Dietary Supplement: Almonds |
| Snack Bar | Active comparator | snack bar group will ingest a matched calorie, common snack bar in split doses (324 calories/day, Nutri-Grain cereal bars, 120 kcal each) Receives: Dietary Supplement: Snack bars |
What is being measured
The primary outcome is the main question the study is designed to answer.
Serum concentration of creatine kinase
Muscle damage biomarker
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Secondary outcomes (9)
Plasma concentrations of pro-inflammatory oxylipins: 19-hydroxy-eicosatetraenoic acid (HETE), 20-HETE, 20-cooh-AA, 8,9-dihydroxy-eicosatrienoic (all ng/ml) acid; (diHETrE), 14,15-diHETrE
Inflammation biomarkers
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Plasma concentration of IL-6
Inflammation biomarkers
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Urine almond metabolites: epicatechin, catechin, epiafzelechin, gallic acid, ellagic acid (all uM)
Almond polyphenol gut-derived metabolites
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
30-second Wingate cycle test watts
Anaerobic sprint power cycling test, peak and average watts
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Leg-back strength kilograms
Muscle performance, leg-back strength with a dynamometer
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Bench press repetitions
Muscle performance, bench press to exhaustion with weighted bar
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Vertical jump height
Vertical jump height as a muscle function test
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Rating of Profile of Mood States (POMS)
Rating scale to assess mood states, energy, vitality; 0 to 4 scale, with 0=not at all and 4 = extremely
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Serum concentration of myoglobin
Muscle damage biomarker
Measured: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jul 2021
- Study start16 Jun 2021
- Primary completion30 Oct 2021
- Study completion30 Oct 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Muscular InjuryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Randomized, parallel groups
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Appalachian State University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- David C Nieman, Principal investigator, Appalachian State Univ
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04958018
- Sponsor's protocol ID
- 20-0102
- Status last verified
- Dec 2021
- First submitted
- 17 Jun 2021
- Last updated
- 16 Dec 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Will provide data upon request.
Study at a glance
From the registry record, last updated by the sponsor on 16 Dec 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Influence of Almond Supplementation on Energy, Performance, and Inflammation Resolution From Exercise-Induced Muscle Damage
- ClinicalTrials.gov ID
- NCT04958018
- Acronym / sponsor ID
- 20-0102
- Conditions
- Muscular Injury
- Keywords
- almonds, exercise, inflammation, oxylipins, cytokines
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Appalachian State UniversityUniversity, hospital or other
- Study start
- 16 Jun 2021 (actual)
- Primary completion
- 30 Oct 2021 (actual)
- Study completion
- 30 Oct 2021 (actual)
- First posted
- 12 Jul 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The PURPOSE of this study is to see if eating almonds for four weeks will reduce muscle damage, soreness, and inflammation during several days of recovery from eccentric exercise.
Detailed description
This will be the first study to determine if 4-weeks ingestion of nutrient-dense almonds improves feelings of energy and vitality, and mitigates post-exercise inflammation (plasma cytokine and oxylipin levels), muscle soreness, and muscle damage. An acute 90-minute bout of eccentric exercise will be used to induce muscle damage and inflammation in a group of 60 relatively untrained male and female adults (ages 30-65 years). Using a randomized, parallel group design, almond supplementation (57 g/d) for a 4-week period prior to the eccentric exercise challenge will be investigated as a countermeasure strategy to exercise-induced muscle damage and inflammation. The control group will ingest a calorie-matched common snack (cereal bars). To improve the potential for capturing an intervention effect, advanced mass spectrometry procedures will be utilized to measure changes in 70 different oxylipins and lipid mediators that are involved in regulating inflammation. C-reactive protein (CRP), six inflammatory cytokines, and muscle damage biomarkers will also be measured. Blood samples (7 total) will be collected before and after the 4-week supplementation period, and then daily during 5 days of recovery from the eccentric exercise bout. The Profile of Mood States (POMS) will be used to measure mood state and specific domains including vigor or activity, and fatigue or inertia. Exercise performance will be measured each time a blood sample is collected using a comprehensive battery that includes vertical jump, leg/back muscle strength, bench press muscle endurance, and anaerobic power (30-second Wingate test).
Participants will be randomized to the almond or typical snack (cereal bars) supplement groups. The parallel group design is being utilized in this study because of the "repeat exercise bout" effect (i.e., post-exercise muscle damage and inflammation are reduced when the same bout is repeated within days and weeks of the first bout). Participants will come to the lab at 7:00 am at the beginning of the 4-week supplementation period, and then Monday (eccentric exercise bout) and Tuesday through Friday (recovery) in an overnight fasted state. The 4-week supplementation period was based on practical issues related to the research design. A 4-week almond supplementation period was commonly used in prior studies and was sufficient to demonstrate favorable blood lipid changes relative to control conditions.
Seven blood samples will be collected and analyzed for various measures of muscle damage, oxylipins, and inflammation. After each of the blood draws, participants will complete the POMS (energy, vitality) and provide a muscle soreness rating (DOMS). Physical activity will be monitored during the entire study using the International Physical Activity Questionnaire (IPAQ). The IPAQ was developed to measure health-related physical activity (PA) in populations. The short version of the IPAQ has been tested extensively and is now used in many international studies.
Study participants will come to the performance lab for orientation to the testing procedures. This will include a review of the consent form, completion of basic questionnaires, and an introduction to the eccentric muscle exercise bout and the strength/power performance testing protocol (about 1.5 hours) (visit #1). This will be followed by another lab session for pre-study measurements and sample collection with subjects in an overnight fasted state (visit #2) (see description below). A 3-day food record will be collected during the end of the 4-week supplementation period to assess the background diet.
Study participants will have to agree to 5 other lab visits during a one-week period (all overnight fasted condition). These lab visits will start at 7:00 am on Monday, with morning visits at 7:00 am on Tuesday through Friday. At each of the 5 lab visits, study participants will come to the lab at 7:00 am not having consumed food or beverages (other than water) for at least the previous 9 hours, and having abstained from vigorous exercise for at least the previous 24-48 hours. The Monday session will take about 2.5 hours (7:00 to 9:30 am), and the Tuesday through Friday sessions will take about 30-45 minutes each. The total amount of time participants will be asked to volunteer for this study is about 8-9 hours at the performance lab.
Participants will be randomized to almond or snack groups, and provided a 4-weeks supply of supplements. Participants in the almond group will consume 57 g almonds each day in split doses (half in the morning, half in the afternoon). Participants in the snack group will ingest a matched calorie, common snack bar in split doses (324 calories/day, Nutri-Grain cereal bars, 120 kcal each).
The daily dose of almonds (57 g) and just under 3 Nutri-Grain cereal bars will provide a distinct difference in nutrient intake. A serving of 57 g of almonds has 324 calories with 12 g of protein, 28 g of fat (17 g from monounsaturated, 6.6 g from polyunsaturated, 2.6 g from saturated), 12 g of carbohydrates and 6.6 g of fiber, 160 mg total polyphenols, and significant amounts of vitamin E (96% RDA), magnesium, manganese, copper, and other minerals.
Baseline Testing (Visit #2) Participants will provide a blood sample using standard phlebotomy procedures. Participants will also provide a spot urine sample, with instructions to capture a mid-stream urine sample in a disposable urine cup. Spot urine samples provide valid metabolite data as indicators of dietary intake. Height, body weight, and body composition will be measured in a private section of the lab. Bioelectrical impedance (BIA) using the seca BIA scale will be used to assess body composition (i.e., the percent of body weight that is fat tissue) and body weight. Participants will remove shoes and socks and stand with bare feet on the seca scale for about 7-10 seconds while grasping side rails with your hands. Percent body fat will also be measured using the BodPod. Participants will sit inside the BodPod with a tight-fitting swim suit for about 10 minutes while body fat is calculated. The Profile of Mood States (POMS) will be administered. Delayed onset of muscle soreness (DOMS) will be assessed using a 1-10 scale.
Participants will perform some light exercises to warm up, followed by five muscle function tests: vertical jump, bench press, leg-back strength, 60-yard shuttle run test, and anaerobic power through the 30-second Wingate test.
- Vertical jump: Participants will first stand erect with the feet flat on the floor and reach as high as possible with both arms and hands (standing reach height). Participants will then squat down and jump as high as possible with one arm and hand, and tap the measuring device on the Vertec vertical jump apparatus (jump height). This will be repeated three times, with the best score recorded as the difference between the jump and standing reach heights.
- Bench press to exhaustion at 50%/75%: Participants will lie down supine on a bench, and with spotters standing on either side attempt to bench press a weighted bar equal to 75% (males) or 50% (females) body weight as many times as possible (to a metronome set at 60 beats/min or 30 lifts/min). The bar must touch a foam block on the chest lightly in the down position, and the arms must be straight in the up position.
- Leg-Back Strength: Leg/lower back strength will be assessed with a dynamometer. With the legs slightly bent at the knee, participants will grasp a bar attached via a chain and a force measuring device with straight arms, and then lift up with maximal effort for several seconds. This will measure the isometric strength of both legs and back, and will be repeated three times.
- 30-Second Wingate Cycling Test, Anaerobic Power: The Lode cycle ergometer will be adjusted to the participant's body weight (7 watts per kilogram). After a warm up, participants will sprint cycle at maximal speed for 30 seconds. The peak power and average power will be recorded and adjusted to body weight.
- 60-Yard Shuttle Run Test: The shuttle run is a test of anaerobic speed endurance and agility, in which participants run to 5 yards, 10 yards, 15 yards, there and back, for a total of 60 yards. This is a ladder shuttle of progressing distances. Four marker cones are placed 5 yards apart. The participant starts from one end, runs 5 yards and back to the start, 10 yards and back, then 15 yards and finishes at the start line. A total of 60 yards is completed. The participant is required to touch the line with their hand at each turn, and runs through the finish line, for a total of five touches. The time to complete the test in seconds is recorded. The score is the best time of three trials.
Testing Sequence, Day of Eccentric Muscle Exercise (Monday) and 4-Days Recovery (Tuesday through Friday):
Participants will come to the lab at 7:00 am in an overnight fasted state (i.e., no food or beverages other than water for at least the previous 9 hours). Participants (on Monday only) will provide a spot urine sample that will be aliquoted, stored in a -80°C freezer, and then sent to Metabolon (Durham, NC) for global metabolomics analysis (to capture metabolite shifts related to almond ingestion). Participants will provide a blood sample, fill in the POMS, and give a DOMS rating. The almond or snack supplements (half dose) will be consumed. Participants will perform some light exercises to warm up, followed by five muscle function tests (same as baseline): vertical jump, bench press, leg-back strength, 60-yard shuttle run test, and anaerobic power through the 30-second Wingate test. Participants will take these performance tests before and after the 90-minute eccentric muscle exercise bout, and each of the following four mornings at the performance lab.
After taking the five performance tests, participants will engage in 90-minutes of eccentric exercise. This protocol induces significant muscle damage and soreness.
Immediately following exercise, participants will provide a muscle soreness rating and a blood sample. Participants will then take the five muscle function tests. Participants will ingest the supplements (half-dose) during the afternoon. Participants will return at 7:00 am in an overnight fasted state four days in a row (Tuesday through Friday) after Monday's eccentric exercise bout, and provide muscle soreness ratings and blood samples followed by ingestion of the supplements (half dose). Following ingestion of the supplements, participants will take the five muscle function tests. Participants will the second half dose of the supplements in the afternoon (Tuesday, Wednesday, Thursday). On Friday morning, participants will take the supplement (half dose) prior to the muscle function tests. During this week of testing, participants will engage in normal training.
The blood and urine samples will be analyzed for a panel of oxylipins, CRP and six cytokines, three muscle damage markers (creatine kinase, myoglobin, LDH), and urine metabolites.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Randomized, parallel groups
| Arm | Type | Receives |
|---|---|---|
| Almond | Experimental | Dietary Supplement: Almonds57 g almonds each day in split doses (half in the morning, half in the afternoon) |
| Snack Bar | Active comparator | Dietary Supplement: Snack barssnack bar group will ingest a matched calorie, common snack bar in split doses (324 calories/day, Nutri-Grain cereal bars, 120 kcal each) |
Who may qualify
- Ages
- 30 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- Male or female, ages 30-65 years.
- Non-smoker.
- Body mass index of 23 to 30 kg/m2.
- Not engaged in regular weight lifting (less than 3 sessions per week).
- Agree to train normally, maintain weight, and avoid the regular use of protein supplements, large-dose vitamin and mineral supplements, herbs, and medications that influence inflammation (especially Advil, Motrin, aspirin, and similar drugs) during the study.
Key exclusion criteria (6 listed)
- Inability to comply with study requirements.
- Engaged in regular weight training (3 or more times a week).
- Pregnant or breastfeeding.
- Any other condition that would interfere with successful completion of the study.
- Current diagnosis of heart disease, diabetes, or cancer (except for skin cancer).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Almondsalmond (Prunus dulcis) consumption | Dietary supplement | Almond |
| Snack bars324 calories/day, Nutri-Grain cereal bars, 120 kcal each | Dietary supplement | Snack Bar |
Primary outcome
Serum concentration of creatine kinase
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Muscle damage biomarker
9 secondary outcomes
Plasma concentrations of pro-inflammatory oxylipins: 19-hydroxy-eicosatetraenoic acid (HETE), 20-HETE, 20-cooh-AA, 8,9-dihydroxy-eicosatrienoic (all ng/ml) acid; (diHETrE), 14,15-diHETrE
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Plasma concentration of IL-6
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Urine almond metabolites: epicatechin, catechin, epiafzelechin, gallic acid, ellagic acid (all uM)
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
30-second Wingate cycle test watts
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Leg-back strength kilograms
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Bench press repetitions
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Vertical jump height
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Rating of Profile of Mood States (POMS)
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Serum concentration of myoglobin
Time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Dec 2021.
- Individual participant dataSharing planned: No. Will provide data upon request.
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Natural History of Shoulder Pathology in Manual Wheelchair Users
Paraplegia, Spinal Cord Injuries
Recruiting
The Intervention Effect of Exercise on Lumbar Multifidus Muscle Injuries
Chronic Non-specific Low Back Pain, Lumbar Multifidus Muscle Injury
Recruiting
A Comparison of the Effects of Combining ESWT With Blood Flow Restriction Therapy in Patients Diagnosed With Lateral Epicondylitis
Lateral Epicondylitis
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
David C Nieman principal investigator
Appalachian State Univ
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Almonds and Snack bars in people with Muscular Injury, run by Appalachian State University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Dec 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Serum concentration of creatine kinase (time frame: Change from pre-exercise to post-exercise (immediately after, and 1-, 2-, 3-, and 4-days after). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Dec 2021.