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RECRUITINGINTERVENTIONAL

Daily Amino Acid Supplementation for People With Parkinson's Disease

Effects of Targeted Amino Acid Supplementation for People With Parkinson's Disease on Amino Acid Profiles and Health Related Markers

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The goal of this clinical trial is to learn if a tailored amino acid supplement works to help adults living with Parkinson's disease to improve nutrition, metabolic function, body composition, and physical and mental function. The main questions it aims to answer are: Does the tailored amino acid supplement increase essential amino acids (nutritional status)? Does the tailored amino acid supplement increase an antioxidant (complex amino acid) and decrease an amino acid associated with oxidative stress? Does the tailored amino acid supplement improve physical and mental health compared to a placebo supplement? Researchers will compare the tailored amino acid supplement to a placebo (a look-alike substance that contains no active ingredients) to see if the tailored amino acid supplements work to support health for people with Parkinson's disease. Participants will: Take the tailored amino acid supplement or a placebo every day for 6 months, visit the lab at baseline, after 3 months, and after 6 months for fasting blood draws, body composition assessment, and physical and mental health testing and keep a diary of their food intake and supplement intake.

Who May Be Eligible (Plain English)

Inclusionary Criteria: - Male and Females. - 60-80 Years. - Previous diagnosis of idiopathic Parkinson's Disease by patient report. - Use of dopamine replacement medication (e.g. levodopa) for at least 2 years. - On a stable dose of dopamine replacement medication for at least 3 months with no plans for change in the next two months. Exclusionary criteria - Apparent cognitive impairment as determined by phone screening (Telephone Interview for Cognitive Status \<29). - Diagnosis of Parkinsonism or atypical Parkinson's Disease. - Prescription of Dopamine antagonist. - Any unstable medical condition. - Any known bleeding disorder or current consumption of blood thinners. - Use of Deep Brain Stimulation. - Gastric or Bowel resection surgery. - Contraindications to blood draw. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusionary Criteria: * Male and Females. * 60-80 Years. * Previous diagnosis of idiopathic Parkinson's Disease by patient report. * Use of dopamine replacement medication (e.g. levodopa) for at least 2 years. * On a stable dose of dopamine replacement medication for at least 3 months with no plans for change in the next two months. Exclusionary criteria * Apparent cognitive impairment as determined by phone screening (Telephone Interview for Cognitive Status \<29). * Diagnosis of Parkinsonism or atypical Parkinson's Disease. * Prescription of Dopamine antagonist. * Any unstable medical condition. * Any known bleeding disorder or current consumption of blood thinners. * Use of Deep Brain Stimulation. * Gastric or Bowel resection surgery. * Contraindications to blood draw.

Treatments Being Tested

DIETARY_SUPPLEMENT

Targeted Amino Acid Supplement

Blend of the essential amino acids (Leucine \& Tryptophan), a conditionally essential amino acids (Arginine \& Taurine), and non-essential amino acids (Glutamate \& Tyrosine) designed to meet the unique nutritional needs of people with Parkinson's disease (PD).

DIETARY_SUPPLEMENT

Control (placebo)

The inert amino acid (alanine) will serve as an isonitrogenous control.

Locations (1)

University of Connecticut
Storrs, Connecticut, United States