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A Study to Evaluate a Supplement Combination in Supporting Weight Loss, Metabolic Health, and Quality of Life

A Consumer Study to Evaluate the Efficacy of a Postbiotic and Prebiotic Supplement Combination in Supporting Weight Loss, Metabolic Health, and Quality of Life

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07608016
Acronym
RESMRESG101
Enrollment
20
Registered
2026-05-27
Start date
2025-10-20
Completion date
2026-05-05
Last updated
2026-06-01

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

Conditions

Metabolic Health, Quality of Life, Weight Loss

Keywords

weight loss, quality of life, metabolic health, supplement, prebiotic, postbiotic, energy

Brief summary

This consumer-use study evaluates the effects of a combined postbiotic and prebiotic supplement regimen on appetite control, cravings, metabolic health, energy, and quality of life in adults aged 18-65 years with a body mass index (BMI) between 25 and 30. Participants will consume one capsule of resM™ GLP-1 Postbiotic and one scoop of resG prebeet ENERGY Prebiotic daily for 60 days. Data will be collected through daily check-ins, weekly surveys, and quality-of-life questionnaires administered through the Chloe mobile application. The primary objective is to evaluate changes in appetite control and food cravings over 60 days of supplementation.

Detailed description

The GLP-1 Optimizer Bundle combines resM™ GLP-1 Postbiotic and resG prebeet ENERGY Prebiotic to support appetite control, cravings, metabolic health, energy, and lifestyle behaviors. This is a prospective, open-label, single-arm consumer-use study conducted over 60 days in approximately 20 adults aged 18-65 years with BMI between 25 and 30. Participants will consume: one capsule of resM™ GLP-1 Postbiotic daily one scoop of resG prebeet ENERGY Prebiotic daily Assessments will be collected electronically through the Chloe mobile application and include: appetite and cravings surveys energy and mood assessments quality-of-life questionnaires lifestyle habit surveys consumer satisfaction assessments The study aims to evaluate consumer-reported changes associated with daily supplementation and lifestyle guidance.

Interventions

DIETARY_SUPPLEMENTCombination Prebiotic and Postbiotic

Participants will take a combined dosage of prebiotic and postbiotic.

Sponsors

Able Biolabs, LLC
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Adults aged 18-65 years BMI between 25 and 30 Generally healthy Willing to comply with study procedures Access to smartphone or internet-enabled device for electronic questionnaires

Exclusion criteria

Pregnant, planning pregnancy, or lactating History of bariatric surgery Prescription weight loss medication use within the past 90 days Current GLP-1 drug use History of substance abuse within the past 6 months Current use of supplements containing overlapping active ingredients Significant medical condition that may interfere with study participation or interpretation of results

Design outcomes

Primary

MeasureTime frameDescription
Change in Appetite Control and Food Cravings Survey Scores Over 60 DaysBaseline through Day 60Participant-reported appetite control and food cravings will be assessed using daily and weekly questionnaires administered through the Chloe mobile application. Survey responses will evaluate changes in hunger, cravings, satiety, and eating behaviors over the study period.

Secondary

MeasureTime frameDescription
Change in Energy and Mood Survey Scores Over 60 DaysBaseline through Day 60Participant-reported energy levels and mood will be assessed using weekly questionnaires administered through the participant management application.
Change in Quality-of-Life Questionnaire Responses Over 60 DaysBaseline, Day 30, and Day 60Quality-of-life assessments will evaluate participant-reported physical well-being, lifestyle habits, and overall satisfaction during the study period.
Participant Satisfaction and Willingness to Continue Product Use at Day 60Day 60End-of-study surveys will assess participant satisfaction, perceived benefits, and willingness to continue using the supplement combination.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026