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Longterm Effects of a Biofield Patch on Anxiety, Sleep, and Energy

RecruitingHealthy volunteers welcome

Clinical Trial on Long-Term Effects of a Biofield Patch on Anxiety, Sleep, and Energy. A Randomized Double-Blind Placebo-Controlled 4-week Trial.

Who can join

Ages 18 to 75 · All sexes · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* Healthy adults of all genders;
* Age 18-75 years (inclusive);
* BMI between 18.0 and 34.9 (inclusive)
* Experiencing intermittent episodes of anxiety on a regular basis, leading to either avoiding specific situations, or experiencing stress both in anticipation of, and during such situations.

  * Specific situations that occur regularly that cause anxiety, for example:

    * Performing specific tasks at work or at home;
    * Inter-personal conflicts at work or at home;
    * Driving or commuting;
    * Fearful and worrying about one's own situation (such as paying bills);
    * Worrying about ongoing problems experienced by others.

Exclusion Criteria:

* Cancer during past 12 months;
* Chemotherapy during past 12 months;
* Currently taking anxiolytic, hypnotic, or anti-depressant prescription medication;
* Currently taking nutritional supplements judged by the study coordinator to negate or camouflage the effects of the test product;
* Participation in another clinical trial study during this trial, involving an investigational product or lifestyle change;
* Serious active illness within past 6 months;
* People who are pregnant, nursing, or trying to become pregnant.

About the study

The goal for this clinical trial is to compare an active biofield non-transdermal skin patch to a placebo patch in people who frequently experience anxiety.

What is being tested

Sponsor: Natural Immune Systems Inc · Participants: 40 · Started: Oct 23, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07353021

Locations in the U.S.

OregonNIS Labs, Klamath Falls

Conditions

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.