A Clinical Trial to Evaluate the Effects of a Supplement on Energy and Mood
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Change in Energy Levels
Study Overview
Brief Summary
This study evaluates the effects of a Liposomal Magnesium Complex supplement on energy and mood. The study is a single-arm, virtual trial in which 60 adult participants consume the supplement daily for 14 days and complete self-reported questionnaires at multiple timepoints.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Be male or female
- •Be aged 18-60
- •Anyone currently experiencing issues regarding all of the following: Low energy, Difficulty regulating mood
- •Anyone who is generally healthy - does not live with any uncontrolled chronic disease.
- •Anyone willing to avoid all other dietary supplements or products containing magnesium for the duration of the trial.
- •Anyone willing to refrain from taking any products, prescription medications, or supplements that target energy, mood, stress, and sleep during the test period.
- •Anyone willing to maintain their current diet, sleep schedule, and activity level for the duration of the study.
- •Resides in the United States.
Exclusion Criteria
- •Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including cancer and mental health disorders.
- •Anyone with a nut allergy or allergies or sensitivities to any of the product ingredients.
- •Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period).
- •Anyone who drinks heavily (i.e., 8 or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men).
- •History of diagnosed psychiatric or mood disorders.
- •History of diagnosed sleep disorders.
- •History of serious illness in the last three months.
- •History of substance abuse.
- •History of kidney disease.
- •History of hormone or endocrine disorders, including but not limited to hypothyroidism, Hashimoto's thyroiditis, polycystic ovarian syndrome (PCOS), and diabetes.
- •Planned surgery during the study period.
- •Currently partaking in another research study or will be partaking in any other research study for the next 2 weeks, or at any point during this study's duration.
- •Anyone unwilling to follow the study protocol.
Arms & Interventions
Liposomal Magnesium Complex
Participants will consume one packet daily by squeezing the contents directly into the mouth.
Intervention: Liposomal Magnesium Complex (Dietary Supplement)
Outcomes
Primary Outcomes
Change in Energy Levels
Time Frame: Baseline, Day 3, Day 7, Day 10, Day 14
Change in self-reported energy levels following daily use of the Liposomal Magnesium Complex supplement, assessed using participant questionnaires.
Change in Mood
Time Frame: Baseline, Day 3, Day 7, Day 10, Day 14
Change in self-reported mood following daily use of the Liposomal Magnesium Complex supplement, assessed using participant questionnaires.
Secondary Outcomes
- Change in Stress Levels(Baseline, Day 3, Day 7, Day 10, Day 14)
- Change in Relaxation and Calmness(Baseline, Day 3, Day 7, Day 10, Day 14)
- Change in Balanced Mood(Baseline, Day 3, Day 7, Day 10, Day 14)
- Change in Sleep Quality(Baseline, Day 3, Day 7, Day 10, Day 14)
- Change in Muscle Tension(Baseline, Day 3, Day 7, Day 10, Day 14)
