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OpenTrials
Completed

NCT Number: NCT07765420

A Clinical Trial to Evaluate the Effects of an Electrolyte Supplement on Women's Wellness

This study evaluates the effects of the Daily Love Electrolytes supplement on women's wellness over a 4-week period. The primary focus is on perceived hydration and energy levels, assessed via self-reported questionnaires at Baseline, Week 1, Week 2, Week 3, and Week 4.

This is a single-arm, open-label, virtual trial enrolling 40 female participants aged 18 and older who have experienced low energy and feelings of dehydration in the past four weeks. All participants will take two electrolyte tablets daily as directed throughout the 4-week study duration.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Citruslabs

Las Vegas, Nevada, 89101, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be female
  • Be aged 18+
  • Anyone experiencing issues regarding all of the following over the past four weeks: low energy and feeling dehydrated
  • Anyone who is generally healthy - does not live with any uncontrolled chronic disease
  • Willing to refrain from taking any products, prescription medications, or supplements that target energy, hydration, and general wellness during the test period
  • Willing to maintain a consistent level of water intake for the duration of the study
  • Willing to avoid other hydration products, including soluble products or pre-made beverages such as Pedialyte or Gatorlyte
  • Willing to maintain current diet, sleep schedule, and activity level for the duration of the study
  • Resides in the United States
  • Not currently partaking in another research study and will not be partaking in any other research study for the next 4 weeks and at any point during this study's duration

Exclusion criteria

  • Anyone with pre-existing chronic conditions that would impact participation in the study, including cancer, mental health disorders, history of serious illness in the last three months, history of substance abuse, or planned surgery during the study period
  • Anyone with any allergies or sensitivities to any of the study product ingredients
  • Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period)
  • Anyone taking prescription Eskalith or Lithobid (lithium)
  • Anyone taking prescription Lanoxin (digoxin)
  • Anyone diagnosed with and is being treated for Parkinson's Disease with prescription medications
  • Anyone taking prescription antibiotics in the study duration
  • Anyone diagnosed with kidney disease
  • Anyone unwilling to follow the study protocol

Treatment and study plan

Daily Love Electrolytes

Dietary Supplement

All 40 participants receive the Daily Love Electrolytes supplement. Two tablets are taken per day (one at 11am and one at 3pm), each dissolved in 16 fl.oz/475 mL of water, with or without food, for 4 weeks.

Primary outcomes

  1. Change in Perceived Hydration

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Mean change in self-reported hydration assessed via questionnaire

  2. Change in Perceived Energy

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Mean change in self-reported energy assessed via questionnaire

Secondary outcomes

  1. Participant Perception of Hydration

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Self-reported perception of the product's effects on hydration assessed via questionnaire

  2. Participant Perception of Energy

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Self-reported perception of the product's effects on energy assessed via questionnaire

  3. Participant Perception of General Feelings of Wellness

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Self-reported perception of general feelings of wellness assessed via questionnaire

  4. Participant Perception of Getting More Out of Diet and Wellness Routines

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Self-reported perception of getting more out of diet and wellness routines assessed via questionnaire

  5. Participant Perception of Bloating

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Self-reported perception of the product's effects on bloating assessed via questionnaire

  6. Participant Perception of Ease of Use

    Time frame: Baseline, Week 1, Week 2, Week 3, and Week 4

    Self-reported perception of the product's ease of use assessed via questionnaire

Sponsors and collaborators

Lead sponsor

Love Wellness

Industry

Collaborators

  • Citruslabs

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Aug 14, 2026
Registry last updated
Aug 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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