What this study is
The goal of this observational study is to learn how health and quality of life change over time in adults and children aged 2 years and older. It will also examine how these changes are related to participation in wellness activities and the use of nutritional supplements.
The main questions this study aims to answer are:
How do measures of health, physical function, and quality of life change over time? Are changes in these measures associated with participation in a wellness program, nutritional supplement use, or other health and lifestyle factors?
Participants may:
Answer questions about their health, lifestyle, physical activity, sleep, fatigue, stress, and quality of life.
Complete physical and functional assessments. Choose to provide blood samples for laboratory testing. Complete follow-up assessments over time.
This is an observational study. Researchers will not assign participants to a wellness program or any other intervention or tell participants which supplements to use. Any wellness program participation or supplement use occurs independently of the study.
Study details
- Official title
- Association Between Participation in a Comprehensive Wellness Program and Changes in Functional, Nutritional, and Quality of Life Outcomes Among Adults and Children - an Observational Study
- Sponsor
- Dr. Goodenowe Research LLC
- Conditions
- Health and Wellness
- Enrolling
- 100 people
- Starts
- 2026-09
- Est. completion
- 2034-09
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 2 Years and overSex ALLHealthy volunteers AcceptedYou may qualify if
- Age 2 years or older
- Able to provide informed consent, or parent or legally authorized representative able to provide informed consent
- Able to provide assent, if age 7 years or older
- Willing and able to complete baseline and follow-up assessments according to the study schedule
- Willing to allow use of wellness program data for research, if enrolling in a wellness program
You can't join if
- Participant or caregiver unable to provide informed consent
- Expected inability to complete follow-up
- Concurrent enrollment in an interventional clinical trial that would substantially confound outcomes of interest
- Any condition that, in the opinion of the investigator, would make participation unsafe or unreliable
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (2)
2 openContact for every open site
- Dayan Goodenowe, PhD · Principal investigator
Restorative Health Center
Temecula, California, United States
- Stan Mokoko Sr, MD, MS-CRA · Sub-investigator
1 site outside the US
Lakeview Regional Wellness Centre
Moose Jaw, Saskatchewan, Canada
Study team
Sponsor
Dr. Goodenowe Research LLC
Study ID DGR-202604
Principal investigator
Dayan Goodenowe, PhD
Dr. Goodenowe Research LLC
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.