Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Not Yet Recruiting NCT07832981

Wellness Program Participation and Changes in Health and Quality of Life in Adults and Children

Conditions: Health and Wellness

Sex: All
Ages: 2 Years – N/A
Healthy volunteers: Yes
Enrollment: 100
Sponsor: Dr. Goodenowe Research LLC

Location: Restorative Health Center Temecula California

Summary

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.

Eligibility Criteria

Inclusion Criteria: * 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 Exclusion Criteria: * 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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07832981). StuddyBuddy aggregates publicly available trial information.