The Effects of the GOLO for Life® Plan and Release Supplement on Weight Management in Overweight and Obese Adults

Golo

Status and phase: Completed; Phase 2

Conditions: Overweight; Obese

Treatments: Dietary Supplement: Release

Study type: Interventional

Funder types: Industry

Identifiers

NCT05844631

22GLCFG01

Details and patient eligibility

About

The objective of this study is to investigate the efficacy and safety of the GOLO for Life® Plan (G4LP) and Release supplementation on weight loss, body composition, and cardiometabolic parameters in overweight and obese adults. The change from baseline at Days 90 and 180 following the G4LP and supplementation with Release in weight (kg and % of total weight) and fat mass (percent and kg) will be assessed by Dual X-Ray Absorptiometry (DEXA). The weekly change in weight (kilograms and percent change) will also be assessed from baseline to day 180 following the G4LP and Release supplementation. Additionally, the safety and tolerability of the G4LP and Release supplementation will be measured by the occurrence of and/or changes in pre-emergent and post-emergent adverse events (AEs).

Enrollment: 83 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Males and females between the age of 18-65 years, inclusive, at screening

2. BMI between 25 and 39.9 kg/m2

3. Females not of child-bearing potential, defined as those who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening

   Or,

   Individuals of child-bearing potential must have a negative baseline urine pregnancy test and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months prior to enrollment. Acceptable methods of birth control include:

   • Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System)
   • Double-barrier method
   • Intrauterine devices
   • Non-heterosexual lifestyle or agrees to use contraception if planning on changing to heterosexual partner(s)
   • Vasectomy of partner at least 6 months prior to screening
   • Abstinence and agrees to use contraception if planning on becoming sexually active

4. Self-reported stable body weight defined as not having gained or lost more than 5 kg of body weight in the three months prior to baseline

5. Motivated and ability to comply with G4LP guidelines as assessed by a Self-Motivation Questionnaire at screening (see Appendix 16.2)

6. Agrees to maintain current lifestyle habits as much as possible throughout the study depending on ability to maintain the following: medications, supplements (unless excluded), and sleep

7. Willingness and ability to complete questionnaires, records, and diaries associated with the study, adhere to dietary and exercise guidelines, and to complete all clinic visits

8. Provided voluntary, written, informed consent to participate in the study

Exclusion criteria

1. Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
2. Allergy, sensitivity, or intolerance to the investigational product ingredients
3. Gastric bypass surgery or other surgeries to induce weight loss
4. Metal implants or other physical characteristics/limitations that may affect DEXA scan results, as assessed by the QI
5. Current participation within the last three months in any weight loss or diet programs
6. Current or history of eating disorders, as assessed by the QI
7. Obesity-induced by metabolic or endocrinologic disorders (ex. acromegaly, hypothalamic obesity), as assessed by the QI
8. Current or history of significant diseases of the gastrointestinal tract, as assessed by the QI
9. Chronic inflammatory diseases, as assessed by the QI
10. Type I diabetes
11. Type 2 diabetes if on insulin treatment
12. History of gout and have had a flare up within 12 months, as assessed by the QI
13. Current unstable diagnosis with kidney and/or liver diseases as assessed by the QI on a case-by-case basis, with the exception of history of kidney stones in participants who are symptom free for 6 months
14. Self-reported confirmation of current or pre-existing thyroid condition. Treatment on a stable dose of medication for at least 3 months will be considered by the QI
15. Major surgery in the past 3 months or individuals who have planned surgery during the course of the study. Participants with minor surgery will be considered on a case-by-case basis by the QI
16. Cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable
17. Current use of any prescribed or over-the counter medications and/or supplements that may affect body weight or metabolism, as assessed by the QI
18. Regular use of tobacco products within 6 months of baseline and during the study period, as assessed by the QI
19. Chronic inhalation and edible use of cannabinoid products (>1 time/month). Occasional users must agree to wash out and abstain during the study period
20. Alcohol intake average of >2 standard drinks per day
21. Alcohol or drug abuse within the last 12 months
22. Clinically significant abnormal laboratory results at screening, as assessed by the QI
23. Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
24. Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
25. Individuals who are unable to give informed consent
26. Any other condition or lifestyle factor, that, in the opinion of the QI, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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83 participants in 1 patient group

Golo for Life® Plan(G4LP) and Release Supplement

Experimental group

Description:

Participants will be instructed to use the resources provided and follow the G4LP for the duration of the study period. Participants will also take one capsule of Release three times a day, to be taken at the beginning of or during each meal, starting on Day 1. If a dose is missed before or during a meal, participants are instructed to take the dose as soon as they remember after the meal. Participants will be advised not to exceed three capsules daily.

Treatment:

Dietary Supplement: Release

Sponsors of this trial

Lead Sponsor

Golo

Collaborating Sponsor

KGK Science