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Stick-On patch promises calm and better sleep – but does it work?

NCT ID NCT07353021

Symptom relief Sponsor: Natural Immune Systems Inc Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This trial tests a non-transdermal biofield patch against a placebo patch in 40 adults who often feel anxious. Over 4 weeks, researchers will measure changes in anxiety, sleep quality, and energy levels. The goal is to see if the patch offers any real benefit beyond a placebo effect.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
non-transdermal biofield patch
What this could lead to
If it works, this could point toward a simple, non-drug option for easing anxiety and improving sleep.
What could go wrong
This is a very small early trial (40 people) testing a device with an unclear mechanism. Results may not be meaningful or generalizable.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Mar 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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.

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder sleep disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anxiety Sleep

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • NIS Labs

    Klamath Falls, Oregon, 97601, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.