- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05844631
The Effects of the GOLO for Life® Plan and Release Supplement on Weight Management in Overweight and Obese Adults
An Open-label Study Evaluating the Effects of the GOLO for Life® Plan and Release Supplement on Weight Management in Overweight and Obese Adults
Study Overview
Study Type
Enrollment (Actual)
Phase
- Phase 2
Contacts and Locations
Study Contact
- Name: Marc Moulin, PhD
- Phone Number: 300 1-226-781-9094
- Email: mmoulin@kgkscience.com
Study Contact Backup
- Name: KGK Science Inc.
- Email: participate@kgkscience.com
Study Locations
-
-
Ontario
-
Lasalle, Ontario, Canada, N9H 1S4
- One Retreat Wellness
-
London, Ontario, Canada, N6B 3L1
- KGK Science Inc.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Males and females between the age of 18-65 years, inclusive, at screening
- BMI between 25 and 39.9 kg/m2
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
- 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
- Motivated and ability to comply with G4LP guidelines as assessed by a Self-Motivation Questionnaire at screening (see Appendix 16.2)
- 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
- 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
- Provided voluntary, written, informed consent to participate in the study
Exclusion Criteria:
- Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
- Allergy, sensitivity, or intolerance to the investigational product ingredients
- Gastric bypass surgery or other surgeries to induce weight loss
- Metal implants or other physical characteristics/limitations that may affect DEXA scan results, as assessed by the QI
- Current participation within the last three months in any weight loss or diet programs
- Current or history of eating disorders, as assessed by the QI
- Obesity-induced by metabolic or endocrinologic disorders (ex. acromegaly, hypothalamic obesity), as assessed by the QI
- Current or history of significant diseases of the gastrointestinal tract, as assessed by the QI
- Chronic inflammatory diseases, as assessed by the QI
- Type I diabetes
- Type 2 diabetes if on insulin treatment
- History of gout and have had a flare up within 12 months, as assessed by the QI
- 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
- 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
- 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
- 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
- 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
- Regular use of tobacco products within 6 months of baseline and during the study period, as assessed by the QI
- Chronic inhalation and edible use of cannabinoid products (>1 time/month). Occasional users must agree to wash out and abstain during the study period
- Alcohol intake average of >2 standard drinks per day
- Alcohol or drug abuse within the last 12 months
- Clinically significant abnormal laboratory results at screening, as assessed by the QI
- Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
- Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
- Individuals who are unable to give informed consent
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Golo for Life® Plan(G4LP) and Release Supplement
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.
|
One capsule of Release will be taken three times per day for 180 days in combination with the G4LP.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The change in weight (kilograms) following the GOLO for Life® Plan (G4LP) and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Change in weight will be assessed by Dual X-Ray Absorptiometry (DEXA).
|
baseline, day 90, day 180
|
The change in weight (percentage of total weight) following the GOLO for Life® Plan (G4LP) and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Change in weight will be assessed by Dual X-Ray Absorptiometry (DEXA).
|
baseline, day 90, day 180
|
The change in fat mass (percent) following the GOLO for Life® Plan (G4LP) and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Change in fat mass will be assessed by Dual X-Ray Absorptiometry (DEXA).
|
baseline, day 90, day 180
|
The change in fat mass (kilograms) following the GOLO for Life® Plan (G4LP) and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Change in fat mass will be assessed by Dual X-Ray Absorptiometry (DEXA).
|
baseline, day 90, day 180
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The change in body mass index (BMI) from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in muscle mass (percent) as assessed by DEXA from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in android fat (percent) as assessed by DEXA from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in gynoid fat (percent) as assessed by DEXA from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in android/gynoid fat ratio as assessed by DEXA from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in sagittal abdominal diameter (SAD) from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in waist circumference from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in hip circumference from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in arm circumference from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in thigh circumference from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in waist-to-hip ratio from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in lipid levels from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Lipid levels will be assessed by triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), non-HDL-C, low-density lipoprotein cholesterol (LDL-C), TC:HDL-C, TG:HDL-C, and LDL-C:HDL-C ratios
|
baseline, day 90, day 180
|
The change in glycemic control as assessed by HbA1c from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in glycemic control as assessed by serum insulin from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in glycemic control as assessed by serum glucose from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in glycemic control as assessed by HOMA-IR from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in blood pressure from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
baseline, day 90, day 180
|
|
The change in gastrointestinal symptoms from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Gastrointestinal symptoms will be assessed by the Modified Gastrointestinal Symptoms Rating Scale (GSRS)
|
baseline, day 90, day 180
|
The change in subjective sleep efficiency, sleep debt, and sleep difficulty from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Changes in sleep will be assessed by the Healthy People Sleep Quality Index (HPSQI).
|
baseline, day 90, day 180
|
The change in stress levels from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Stress levels will be assessed by the Perceived Stress Scale (PSS) and salivary cortisol.
|
baseline, day 90, day 180
|
The change in physical activity from baseline at Days 90 and 180 following the G4LP and supplementation with Release.
Time Frame: baseline, day 90, day 180
|
Physical activity will be assessed by the International Physical Activity Questionnaire (IPAQ).
|
baseline, day 90, day 180
|
The weekly change in weight (kilogram) from baseline at Day 180 following the G4LP and supplementation with Release.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
The weekly change in weight (percentage) from baseline at Day 180 following the G4LP and supplementation with Release.
Time Frame: baseline to day 180
|
baseline to day 180
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The incidence of pre-emergent and post-emergent adverse events (AE).
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in heart rate (HR)) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in aspartate aminotransferase (AST) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in alanine aminotransferase (ALT) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in alkaline phosphatase (ALP) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in total bilirubin after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in creatinine after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in electrolytes after 180 days.
Time Frame: baseline to day 180
|
Electrolytes to be measured include sodium, potassium, and chloride.
|
baseline to day 180
|
Clinically relevant changes in estimated glomerular filtration rate (eGFR) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in white blood cell (WBC) count with differential after 180 days.
Time Frame: baseline to day 180
|
White blood cells to be measured include neutrophils, lymphocytes, monocytes, eosinophils, and basophils.
|
baseline to day 180
|
Clinically relevant changes in red blood cell (RBC) count after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in hemoglobin after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in hematocrit after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in platelet count after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in immature granulocytes after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in nucleated red blood cells (RBC) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in red blood cell (RBC) mean corpuscular volume (MCV) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in mean corpuscular hemoglobin (MCH) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in mean corpuscular hemoglobin concentration (MCHC) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
|
Clinically relevant changes in red blood cell distribution width (RDW) after 180 days.
Time Frame: baseline to day 180
|
baseline to day 180
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: David Crowley, MD, KGK Science Inc.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 22GLCFG01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Overweight
-
University Hospital, LilleNational Research Agency, France; European Union; University of Lille Nord de... and other collaboratorsNot yet recruitingOverweight and Obesity | Overweight, Childhood | Overweight, Infant
-
Children's Hospital Los AngelesUniversity of Southern California; Tufts Medical CenterRecruitingOverweight and Obesity | Overweight AdolescentsUnited States
-
University of AarhusThe Danish Dairy Research Foundation, Denmark; Sygekassernes HelsefondCompletedOverweight and Obesity | Overweight Adolescents | Metabolic DiseaseDenmark
-
Memorial Sloan Kettering Cancer CenterRecruitingObesity | Overweight | Overweight and Obesity | Obese | Overweight or ObesityUnited States
-
University Hospital Bispebjerg and FrederiksbergUniversity of CopenhagenCompleted
-
Holbaek SygehusUniversity of Copenhagen; University of Florida; University of Minnesota; Hebrew... and other collaboratorsRecruitingChildhood Overweight and ObesityDenmark
-
Khyber Medical University PeshawarRecruitingObesity, OverweightPakistan
-
National Taiwan University HospitalCompleted
-
Institut Investigacio Sanitaria Pere VirgiliCompletedObesity, Childhood | Overweight and Obesity | Overweight, ChildhoodSpain
-
Children's Hospital SrebrnjakBelupo; Podravka d.d.RecruitingBody Weight | Overweight and ObesityCroatia
Clinical Trials on Release
-
Christine M. Kleinert Institute for Hand and MicrosurgeryUnknownMedian Nerve CompressionUnited States
-
Hawler Medical UniversityCompleted
-
Hangzhou Highlightll Pharmaceutical Co., LtdCompleted
-
Cedars-Sinai Medical CenterCompleted
-
PfizerViiV HealthcareCompleted
-
Sehat Medical ComplexCompletedPiriformis SyndromePakistan
-
Cardenal Herrera UniversityCompletedGastroesophageal Reflux DiseaseSpain
-
Heptares Therapeutics LimitedQuotient ClinicalCompletedAlzheimer's DiseaseUnited Kingdom
-
Riphah International UniversityRecruitingPain | Gait | Plantar FascitisPakistan
-
Abant Izzet Baysal UniversityCompletedPain | Anxiety | Trapezius Muscle StrainTurkey