NCT00292656

Brief Summary

Background: It has been suspected in our clinic patients that when patients do not wash their hands after receiving NAET treatments, the effect of their treatments has been reduced or in some cases, the same treatment has to be repeated more times to be effective. Location of the study: PNIB Research Center 6714 Beach Blvd. Buena Park, CA 90621 Purpose The purpose of the study was to determine the importance of hand-washing with plain water after each NAET® treatment. The study utilized an experimental design with random assignment to two groups, consisting of treatment/experimental, and treatment/control groups. Objective: We sought to determine if there is any benefit to mandate hand-washing with plain water after each NAET® treatment.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P75+ for phase_1

Timeline
Completed

Started Dec 2005

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2005

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2005

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

February 15, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 16, 2006

Completed
Last Updated

April 4, 2006

Status Verified

February 1, 2006

First QC Date

February 15, 2006

Last Update Submit

April 2, 2006

Conditions

Allergy

Keywords

Allergy

Outcome Measures

Primary Outcomes (1)

  • We sought to determine if there is any benefit to mandate hand-washing with plain water after each NAET® treatment.

Secondary Outcomes (1)

  • Educational

Interventions

NAETPROCEDURE

Eligibility Criteria

Age22 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Allergy -

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

6714 Beach blvd.

Buena Park, California, 90621, United States

Location

MeSH Terms

Conditions

Hypersensitivity

Condition Hierarchy (Ancestors)

Immune System Diseases

Study Officials

  • Devi S. Nambudripad, DC,LAc.,PhD.

    NAR Foundation

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
NON RANDOMIZED
Masking
DOUBLE
Purpose
ECT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

February 15, 2006

First Posted

February 16, 2006

Study Start

December 1, 2005

Study Completion

December 1, 2005

Last Updated

April 4, 2006

Record last verified: 2006-02

Locations

US(1)