NCT07765420

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 7, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 6, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 6, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

August 11, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 14, 2026

Completed
Last Updated

August 14, 2026

Status Verified

August 1, 2026

Enrollment Period

7 months

First QC Date

August 11, 2026

Last Update Submit

August 11, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change in Perceived Hydration

    Mean change in self-reported hydration assessed via questionnaire

    Baseline, Week 1, Week 2, Week 3, and Week 4

  • Change in Perceived Energy

    Mean change in self-reported energy assessed via questionnaire

    Baseline, Week 1, Week 2, Week 3, and Week 4

Secondary Outcomes (6)

  • Participant Perception of Hydration

    Baseline, Week 1, Week 2, Week 3, and Week 4

  • Participant Perception of Energy

    Baseline, Week 1, Week 2, Week 3, and Week 4

  • Participant Perception of General Feelings of Wellness

    Baseline, Week 1, Week 2, Week 3, and Week 4

  • Participant Perception of Getting More Out of Diet and Wellness Routines

    Baseline, Week 1, Week 2, Week 3, and Week 4

  • Participant Perception of Bloating

    Baseline, Week 1, Week 2, Week 3, and Week 4

  • +1 more secondary outcomes

Study Arms (1)

Daily Love Electrolytes

EXPERIMENTAL
Dietary Supplement: Daily Love Electrolytes

Interventions

Daily Love ElectrolytesDIETARY_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.

Daily Love Electrolytes

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Citruslabs

Las Vegas, Nevada, 89101, United States

Location

MeSH Terms

Conditions

Dehydration

Condition Hierarchy (Ancestors)

Water-Electrolyte ImbalanceMetabolic DiseasesNutritional and Metabolic DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 11, 2026

First Posted

August 14, 2026

Study Start

April 7, 2025

Primary Completion

November 6, 2025

Study Completion

November 6, 2025

Last Updated

August 14, 2026

Record last verified: 2026-08

Locations