NCT07765407

Brief Summary

This study evaluates the effects of Love Wellness Energize, a dietary supplement, on supporting signs of a healthy metabolism in women aged 25-45 who report poor energy levels, perception of poor metabolism, difficulty with weight management, and feeling bloated. The trial is a single-arm, open-label, virtual study conducted over 4 weeks with 40 female participants. Participants will dissolve one tablet of the test product in 16 fl.oz/475 mL of water twice daily and complete self-reported questionnaires at Baseline, Week 1, Week 2, Week 3, and Week 4. The primary endpoint is change in metabolism support, and secondary endpoints include perceptions of energy, bloating after hydration, and weight management support.

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 8, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 29, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 29, 2025

Completed
1.2 years 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

2 months

First QC Date

August 11, 2026

Last Update Submit

August 11, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Healthy Metabolism Support

    Self-reported perception of metabolism support, assessed via self-reported questionnaire

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

Secondary Outcomes (3)

  • Change in Self-Reported Energy

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

  • Change in Self-Reported Bloating After Hydration

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

  • Change in Self-Reported Weight Management Support

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

Study Arms (1)

Love Wellness Energize

EXPERIMENTAL
Dietary Supplement: Love Wellness Energize

Interventions

Love Wellness EnergizeDIETARY_SUPPLEMENT

All participants dissolve one tablet of Love Wellness Energize in 16 fl.oz/475 mL of water twice daily at 11 am and 3 pm (or after planned exercise) for 4 weeks. Ingredients include Vitamin B1 15 mg, Vitamin B3 30 mg, Vitamin B6 10 mg, Vitamin B12 250 mcg, Calcium 100 mg, Magnesium 60 mg, Chromium 200 mcg, Sodium 310 mg, and Potassium 200 mg, among other excipients.

Love Wellness Energize

Eligibility Criteria

Age25 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Be female.
  • Be aged 25-45.
  • Currently experiencing issues regarding all of the following: poor energy levels, perception of poor metabolism, difficulty with weight management, and feeling bloated.
  • Generally healthy - does not live with any uncontrolled chronic disease.
  • Willing to refrain from taking any products, prescription medications, or supplements that target metabolic health during the test period.
  • Willing to maintain their current diet, sleep schedule, and activity level for the study duration.
  • Resides in the United States.

You may not qualify if:

  • Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, 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 diagnosed with and getting treated for Parkinson's disease.
  • Anyone taking a prescription diabetes medication including but not limited to GLP-1 receptor agonist medications such as Ozempic, Wegovy, or Mounjaro.
  • 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).
  • Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period).
  • Anyone testing or planning to test, in the next 4 weeks, a product for another research study.
  • Anyone unwilling to follow the study protocol.
  • Anyone with any allergies or sensitivities to any of the study product ingredients.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Citruslabs

Las Vegas, Nevada, 89101, United States

Location

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 8, 2025

Primary Completion

May 29, 2025

Study Completion

May 29, 2025

Last Updated

August 14, 2026

Record last verified: 2026-08

Locations