Rapid Effects of a Biofield Patch on Antioxidant Status and Cellular Energy

Conditions

• Antioxidant Status

Eligibility Criteria

Sex

ALL

Age

18 Years - 75 Years

Healthy Volunteers

Accepted

Interventions

• Active dermal patch — OTHER
  Non-transdermal patch
• Placebo dermal patch — OTHER
  Non-transdermal patch

Study Details

The goal for this clinical proof-of-concept study is to compare an active biofield skin patch to a placebo patch on antioxidant function and mitochondrial function. A double-blind, placebo-controlled cross-over study design will be used.

Key Dates

Start date

Dec 4, 2025

Status verified

Dec 2025

Primary completion

Jul 31, 2026

Completion

Aug 31, 2026

Study Design

Enrollment

12 participants (estimated)

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

BASIC_SCIENCE

Arms

• Experimental: Experimental: Crossover group 1, randomized
  Participants wear an active biofield patch versus a placebo patch for 12 hours on each of the two clinic days, at least 1 week apart, allowing for 1 week wash-out period between each patch. The order of interventions for this group is A, B. Following the blinded phase there will be an open-label phase where participants wear the active patch each day for 1 week until the final clinic visit.
• Experimental: Experimental: Crossover group 2, randomized
  Participants wear a placebo patch versus an active biofield patch for 12 hours on each of the two clinic days, at least 1 week apart, allowing for 1 week wash-out period between each product. The order of interventions for this group is B, A. Following the blinded phase there will be an open-label phase where participants wear the patch each day for 1 week until the final clinic visit.

Primary Outcome Measure

Antioxidant protection [ Time Frame: Baseline, 1 hour, and 2 hours after applying a patch. ]

Central Contacts

• Giite S Jensen, PhD
  5418820112
  [email protected]
• Alex Cruickshank

Locations (1)

Find similar trials in Klamath Falls, OR