Radicle Calm 24: A Study of Health and Wellness Products on Feelings of Anxiety and Related Health Outcomes

Anxiety Clinical Trial

Official title:

Radicle Calm™ 24: A Randomized, Double-Blind, Placebo-Controlled Direct-to-Consumer Study Assessing the Impact of Health and Wellness Products on Feelings of Anxiety and Related Health Outcomes

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06431074
• Other study ID #: RADX-P-2402
• Status: Recruiting
• Phase: N/A
• Start date: May 30, 2024
• Est. completion date: December 2024

Study information

• Verified date: May 2024
• Source: Radicle Science
• Contact: Study Manager
• Phone: 760-281-3898
• Email: studymgmt[@]radiclescience.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A randomized, double-blind, placebo-controlled study assessing the impact of health and wellness products on feelings of anxiety and related health outcomes

Description:

This is a randomized, double-blind, placebo-controlled study conducted with adult participants, residing in the United States.

Eligible participants will (1) endorse a desire for less feelings of anxiety (2) have the opportunity for meaningful improvement (at least 30%) in their primary health outcome, and (3) express acceptance in taking a product and not knowing its formulation until the end of the study.

Participants that report a known cardiac dysfunction, liver or kidney disease may be excluded. Participants that report a known contraindication or with well-established, significant safety concerns due to illness will be excluded. Heavy drinkers and those who report they are pregnant, trying to become pregnant, or breastfeeding will be excluded. Participants that report taking medications with a known contraindication or with well-established, significant safety concerns will be excluded.

Self-reported data are collected electronically from eligible participants over 7 weeks. Participant reports of health indicators will be collected at baseline, throughout the active period of study product use, and in a final survey. All study assessments will be electronic; there are no in-person visits or assessments for this real-world evidence study.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 500
• Est. completion date: December 2024
• Est. primary completion date: August 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years to 105 Years

Eligibility

Inclusion Criteria:

• Adults, at least 21 years of age and older at the time of electronic consent, inclusive of all ethnicities, races, genders and/or gender identities. Assigned sex at birth will determine sex-specific recruitment and surveys (male vs female) employed, when needed

• Resides in the United States

• Endorses less anxiety as a primary desire

• Has the opportunity for at least 20% improvement in their primary health outcome

• Expresses a willingness to take a study product and not know the product identity (active or placebo) until the end of the study

Exclusion Criteria:

• Reports being pregnant, trying to become pregnant, or breastfeeding

• Unable to provide a valid US shipping address and mobile phone number

• Reports current enrollment in another clinical trial

• Reports being a heavy drinker (defined as drinking 3 or more alcoholic beverages per day)

• Unable to read and understand English

• Reports a current and/or recent (up to 3 months ago) major illness and/or surgery that poses a known, significant safety risk.

• Reports a diagnosis of cardiac dysfunction, liver or kidney disease that presents a known contraindication and/or a significant safety risk with any of the study product ingredients. NYHA (New York Heart Association) Class Ill or IV congestive heart failure, atrial fibrillation, uncontrolled arrhythmias, cirrhosis, end-stage liver disease, stage 3b or 4 chronic kidney disease, or kidney failure

• Reports taking medications that have a well-established moderate or severe interaction, posing a substantial safety risk with any of the study product ingredients. Anticoagulants, antihypertensive, anxiolytics, antidepressants, chemotherapy, immunotherapy, sedative hypnotics, seizure medications, medications that warn against grapefruit consumption, corticosteroids at doses greater than 5 mg per day, diabetic medications, oral anti-infectives (antibiotics, antifungals, antivirals) to treat an acute infection, antipsychotics, MAOls (monoamine oxidase inhibitors), or thyroid products

• Reports current use of the primary ingredient(s) and/or similar product(s) to the active study product(s)

• Lack of reliable daily access to the internet

Related Conditions & MeSH terms

• Anxiety
• Anxiety Disorders
• Stress

Intervention

Dietary Supplement:
• Placebo Control Form 1
Participants will use their Placebo Control Form 1 as directed for a period of 6 weeks.
• Calm Active Study Product 1.1 Usage
Participants will use their Radicle Calm Active Study Product 1.1 as directed for a period of 6 weeks.

Locations

Country	Name	City	State
United States	Radicle Science, Inc	Del Mar	California

Sponsors (1)

Lead Sponsor	Collaborator
Radicle Science

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (1)	Mean difference in saliva concentration as assessed by saliva-based IgG (Immunoglobulin) biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (2)	Mean difference in saliva concentration as assessed by saliva-based cytokines (Interleukin 1 beta, Interleukin 8, Tumor necrosis factor-alpha, and Interleukin 6) biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (3)	Mean difference in saliva concentration as assessed by saliva-based dehydroepiandrosterone sulfate (DHEA-S) biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (4)	Mean difference in saliva concentration as assessed by saliva-based estradiol biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (5)	Mean difference in saliva concentration as assessed by saliva-based progesterone biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (6)	Mean difference in saliva concentration as assessed by saliva-based testosterone biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (7)	Mean difference in saliva concentration as assessed by saliva-based cortisol biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (8)	Mean difference in saliva concentration as assessed by saliva-based melatonin biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in saliva concentration of at-home (direct-to-consumer) specimen assay (9)	Mean difference in saliva concentration as assessed by saliva-based C-Reactive Protein (CRP) biomarker. (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (1)	Mean difference in blood concentration as assessed by blood-based cortisol biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (2)	Mean difference in blood concentration as assessed by blood-based homocysteine biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (3)	Mean difference in blood concentration as assessed by blood-based ferritin biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (4)	Mean difference in blood concentration as assessed by blood-based thyroid stimulating hormone (TSH) biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (5)	Mean difference in blood concentration as assessed by blood-based hemoglobin A1C (HbA1c) biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (6)	Mean difference in blood concentration as assessed by blood-based insulin biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (7)	Mean difference in blood concentration as assessed by blood-based vitamin D biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (8)	Mean difference in blood concentration as assessed by blood-based dehydroepiandrosterone sulfate (DHEA-S) biomarker (1 drop). (Optional; among consented male participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (9)	Mean difference in blood concentration as assessed by blood-based testosterone biomarker (1 drop) (Optional; among consented male participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (10)	Mean difference in blood concentration as assessed by blood-based estradiol biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (11)	Mean difference in blood concentration as assessed by blood-based follicle-stimulating hormone (FSH) biomarker (1 drop). (Optional; among consented female participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (12)	Mean difference in blood concentration as assessed by blood-based total cholesterol (high-density lipoproteins (HDL) and low-density lipoproteins (LDL)) biomarker (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in blood concentration of at-home (direct-to-consumer) specimen assay (13)	Mean difference in blood concentration as assessed by blood-based triglycerides (apolipoprotein A1 (ApoA1) and apolipoprotein B (ApoB)) (1 drop). (Optional; among consented participants only).	6 weeks
Other	Change in stool concentration of at-home (direct-to-consumer) specimen assay	Mean difference in stool concentration as assessed by a stool sample (microbial diversity) (Optional; among consented participants only).	6 weeks
Primary	Change in feelings of anxiety	Mean difference in feelings of anxiety score as assessed by Patient Reported Outcome Measurement System (PROMIS) Anxiety 8A (scale 8-40; where lower scores correspond to less feelings of anxiety)	6 weeks
Secondary	Change in stress	Mean difference in stress score as assessed by Perceived Stress Scale 4 (PSS-4) (scale 0-16; where lower scores correspond to less stress)	6 weeks
Secondary	Change in sleep	Mean difference in sleep score as assessed by Patient Reported Outcome Measurement System (PROMIS) Sleep Disturbance 4A (scale 4-20; where lower scores correspond to better sleep quality/less sleep disturbance)	6 weeks
Secondary	Change in mood (emotional distress)	Mean difference in mood score as assessed by Patient Reported Outcome Measurement System (PROMIS) Emotional Distress-Depression 4A (scale 4-20; where lower scores correspond to lower levels of emotional distress)	6 weeks
Secondary	Minimal clinically important difference (MCID) in feelings of anxiety	Likelihood of achieving a MCID in sleep disturbance, as measured by Patient Reported Outcome Measurement System (PROMIS) Anxiety 8A (scale 8-40; where lower scores correspond to less feelings of anxiety)	6 weeks
Secondary	Minimal clinically important difference (MCID) in stress	Likelihood of experiencing minimal clinically important difference in stress score as assessed by Perceived Stress Scale 4 (PSS-4) (scale 0-16; where lower scores correspond to less stress)	6 weeks
Secondary	Minimal clinically important difference (MCID) in sleep	Likelihood of experiencing minimal clinically important difference in sleep score as assessed by Patient Reported Outcome Measurement System (PROMIS) Sleep Disturbance 4A (scale 4-20; where lower scores correspond to better sleep quality/less sleep disturbance)	6 weeks
Secondary	Minimal clinically important difference (MCID) in mood (emotional distress)	Likelihood of experiencing minimal clinically important difference in mood score as assessed by Patient Reported Outcome Measurement System (PROMIS) Emotional Distress-Depression 4A (scale 4-20; where lower scores correspond to lower levels of emotional distress)	6 weeks

External Links

•   Radicle Science, Inc