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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07765420
Enrollment
40
Registered
2026-08-14
Start date
2025-04-07
Completion date
2025-11-06
Last updated
2026-08-14

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

Conditions

Bloating, Dehydration, Low Energy, Women's Wellness

Brief summary

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.

Interventions

DIETARY_SUPPLEMENTDaily Love Electrolytes

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.

Sponsors

Love Wellness
Lead SponsorINDUSTRY
Citruslabs
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change in Perceived HydrationBaseline, Week 1, Week 2, Week 3, and Week 4Mean change in self-reported hydration assessed via questionnaire
Change in Perceived EnergyBaseline, Week 1, Week 2, Week 3, and Week 4Mean change in self-reported energy assessed via questionnaire

Secondary

MeasureTime frameDescription
Participant Perception of HydrationBaseline, Week 1, Week 2, Week 3, and Week 4Self-reported perception of the product's effects on hydration assessed via questionnaire
Participant Perception of EnergyBaseline, Week 1, Week 2, Week 3, and Week 4Self-reported perception of the product's effects on energy assessed via questionnaire
Participant Perception of General Feelings of WellnessBaseline, Week 1, Week 2, Week 3, and Week 4Self-reported perception of general feelings of wellness assessed via questionnaire
Participant Perception of Getting More Out of Diet and Wellness RoutinesBaseline, Week 1, Week 2, Week 3, and Week 4Self-reported perception of getting more out of diet and wellness routines assessed via questionnaire
Participant Perception of BloatingBaseline, Week 1, Week 2, Week 3, and Week 4Self-reported perception of the product's effects on bloating assessed via questionnaire
Participant Perception of Ease of UseBaseline, Week 1, Week 2, Week 3, and Week 4Self-reported perception of the product's ease of use assessed via questionnaire

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026