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Clinical Trials/NCT07398521
NCT07398521CompletedNot Applicable

A Clinical Trial to Evaluate the Effects of a Supplement on Energy and Mood

Cymbiotika, LLC1 site in 1 country60 target enrollmentStarted: October 14, 2025Last updated:
Interventions

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

Experimental

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)

Investigators

Sponsor
Cymbiotika, LLC
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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