A Study to Evaluate a Supplement Combination in Supporting Weight Loss, Metabolic Health, and Quality of Life
RESMRESG101
A Consumer Study to Evaluate the Efficacy of a Postbiotic and Prebiotic Supplement Combination in Supporting Weight Loss, Metabolic Health, and Quality of Life
1 other identifier
interventional
20
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
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
October 20, 2025
CompletedFirst Submitted
Initial submission to the registry
April 29, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 5, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 5, 2026
CompletedFirst Posted
Study publicly available on registry
May 27, 2026
CompletedJune 1, 2026
May 1, 2026
7 months
April 29, 2026
May 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Appetite Control and Food Cravings Survey Scores Over 60 Days
Participant-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.
Baseline through Day 60
Secondary Outcomes (3)
Change in Energy and Mood Survey Scores Over 60 Days
Baseline through Day 60
Change in Quality-of-Life Questionnaire Responses Over 60 Days
Baseline, Day 30, and Day 60
Participant Satisfaction and Willingness to Continue Product Use at Day 60
Day 60
Study Arms (1)
Active Supplement Bundle
EXPERIMENTALresM™ GLP-1 Postbiotic, and resG prebeet ENERGY Prebiotic
Interventions
Participants will take a combined dosage of prebiotic and postbiotic.
Eligibility Criteria
You may qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Able Biolabs, LLC
Birmingham, Alabama, 35203, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 29, 2026
First Posted
May 27, 2026
Study Start
October 20, 2025
Primary Completion
May 5, 2026
Study Completion
May 5, 2026
Last Updated
June 1, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share