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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05523115
Other study ID # 20250
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 15, 2022
Est. completion date October 1, 2022

Study information

Verified date November 2022
Source Heights
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Smart Supplement has 20 vitamins and minerals that have strong track records of demonstrating positive health effects, both physiologically and cognitively. This twelve-week trial will examine the effectiveness and efficacy of Heights Smart Supplement on both biomarkers and subjective experiences from participants.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date October 1, 2022
Est. primary completion date October 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 70 Years
Eligibility Inclusion Criteria: - In good general health with no major chronic conditions - Must experience one of the following issues: brain fog - OR issues with fatigue, - OR sleep issues, - OR trouble with focus and concentration, - OR lead a busy, stressful life. - Must have a fitness tracker that they use to track sleep behaviors. - May be on a vegan/vegetarian diet Exclusion Criteria: - Females who are pregnant or breastfeeding - Anyone currently taking other supplements focused on brain health, or multi vitamins, including additional iron supplements - Anyone taking Thyroxine and Levothyroxine - Anyone taking antidepressants (such as Sertraline or SSRIs like fluoxetine) - Anyone on hormone replacement therapy - Anyone taking blood pressure medication (such as linosipril) - Anyone with a known allergic reaction - Any chronic conditions, including oncological and psychiatric disorders

Study Design


Intervention

Dietary Supplement:
Heights Smart Supplement
The ingredient list of the product includes the following: Algae oil Blueberry Extract Methylcobalamin (Vitamin B12) Cholecalciferol (Vitamin D3) Ascorbic acid (Vitamin C) Retinol acetate (Vitamin A) Calcium L-methylfolate (Folic Acid) D-biotin Pyridoxine hydrochloride (Vitamin B6) Calcium pantothenate (Vitamin B5) Nicotinamide (Vitamin B3) Riboflavin (Vitamin B2) Thiamine hydrochloride (Vitamin B1) D-Alpha tocopheryl acetate (Vitamin E) Chromium picolinate Potassium iodide Iron Citrate Sodium selenite Zinc citrate

Locations

Country Name City State
United States Citruslabs Santa Monica California

Sponsors (2)

Lead Sponsor Collaborator
Heights Citruslabs

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Measures of C-reactive protein Biomarkers measured by a third party lab through blood samples submitted by participants. 12 weeks
Primary Changes in Measures of cortisol Biomarkers measured by a third party lab through blood samples submitted by participants. 12 weeks
Primary Changes in Sleep Quality as measured via Fitness trackers and Questionnaires Measurements taken via existing smart watches and report that data on the questionnaires. 12 weeks
Secondary examine the subjective experiences of participants taking the Heights Smart Supplement. The questionnaires for this study are specifically designed to understand changes in focus, anxiety embedded in mood & stress, memory, and overall well-being. 12 weeks
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