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The Effects of Orally Ingesting Branched Chained Amino Acids on Delayed Onset Muscle Soreness in Diabetic Patients

The Effects of Orally Ingesting Branched Chained Amino Acids on Delayed Onset Muscle Soreness in Diabetic Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01211717
Enrollment
50
Registered
2010-09-29
Start date
2010-10-31
Completion date
2011-04-30
Last updated
2011-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Individuals, Type 2 Diabetes

Keywords

Branched Chained Amino Acids, Delayed Onset Muscle Soreness, Diabetes, Muscle Damage

Brief summary

The purpose of this study is to determine the effectiveness of the 3 Branched Chained Amino Acids (isoleucine, leucine, and valine) on treating Delayed Onset Muscle Soreness, a type of muscle pain which usually develops after exercising.

Detailed description

Delayed Onset Muscle Soreness is a common painful sensation experienced by individuals who have been recently inactive and begin with an unaccustomed exercise protocol. Branched Chained Amino Acids have been found as a useful supplement for promoting muscle recovery following exercise; however the effects of this supplement have not been investigated amongst individuals with diabetes.

Interventions

DIETARY_SUPPLEMENTBranched Chained Amino Acids

Two doses of the Branched Chained Amino Acid supplement will be taken. The first dose will be taken 35 minutes before the intended exercise, and the other dose will be taken right after completing the exercise. The amount of the Branched Chained Amino Acid supplement administered to the subjects in the experimental group will vary from one person to the other but a total dose of 1 gram of BCAA per kilogram of lean body mass will be used. This dose will be divided in half and administered at the two specified occasions. The ratio of isoleucine, leucine, and valine will be 1:2.5:1 respectively

OTHERCellulose Placebo mix

The control group will also take 2 doses, 1 before the exercise, and the other after completing the exercise. This dose will be divided in half and administered at the two specified occasions.

Sponsors

Loma Linda University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* The subjects with diabetes must have been diagnosed with diabetes at least one year before the onset of the study * At least 6 weeks of physical inactivity in the upper body * BMI less than 40

Exclusion criteria

* For the Diabetics, hemoglobin A1c levels over 13 * Pregnant * Have Cardiovascular diseases * Have Hepatic diseases * Are diagnosed with Rhabdomyolysis * Recent upper limb injuries * Upper limb neuropathy * Blood Pressure levels over 140/90, or lower than 90/60 * Are on High doses of alpha or beta agonist/antagonists, and take any types of NSAID's, Cox 2 inhibitors, Calcium channel blockers, Pre-Gabalin's, or Pain reducers

Design outcomes

Primary

MeasureTime frame
Measuring Pain, using the short form McGill pain questionnaire5 days following the initial exercise

Secondary

MeasureTime frame
Measuring Muscle strength of the studied muscle5 days following the initial exercise

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026