Food Allergen Eliminations and Combined Protocols for Obesity Reduction: a Preliminary Comparison Study

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03821818

Enrollment

Registered

2019-01-30

Start date

2018-03-05

Completion date

2019-08-30

Last updated

2019-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Food Hypersensitivity, Exercise

Brief summary

Screened subjects will be tested for hidden food allergies. Subjects will eliminate all food that showed leukocyte reactions for 90-days. Subjects will then also be invited to use the Willis Exercise protocol. Body composition testing and Body Mass Index calculation will be accomplished at enrollment and after completion of the 90-day study.

Detailed description

Subjects will first be screened for cardiovascular pathologies and then tested for hidden food allergies. After the results subjects will eliminate all food that showed leukocyte reactions for 90-days. Subjects will then also be invited to use the Willis Exercise protocol (Aerobic-surge exercise \> 75% max heart rate, for 2-minutes, 5/day. Body composition testing and Body Mass Index calculation will be accomplished at enrollment and after completion of the 90-day study.

Interventions

BEHAVIORALFood Allergy Elimination + Willis Exercise

Food Allergy Elimination + Willis Exercise (performing a 2-minute Aerobic-surge exercise \> 75% max heart rate, 5/day)

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

20 Years to 75 Years

Healthy volunteers

Yes

Inclusion criteria

1. The subject is \> 20 years of age and is willing and able to provide signed informed consent. 2. The subject has a BMI \> 30. 3. The subject is between the ages of 20 to 75 years of age.

Exclusion criteria

1. Cardiovascular Heart Disease and this includes but is not limited to history of myocardial infarction, atrial fibrillation, etc. 2. History of cerebral vascular event (stroke), traumatic brain injury, Parkinson's disease or any other neural injury or disease. 3. Diabetes Mellitus (Type I or II) 4. Pregnancy 5. Participation in any other weight loss protocols, diets, or medication.

Design outcomes

Primary

Measure	Time frame	Description
Change in Body Weight	90-days	measure Kg

Secondary

Measure	Time frame	Description
Change in Body Fat %	90-days	Percentage of fat vs lean mass
Change in Body Mass Index (BMI)	90-days	BMI calculation

Countries

United States

Contacts

Primary ContactFrank B Willis, MBBS, PhD

DocWillis@yahoo.com409-457-7894

Backup ContactTina West RN, RN

TinaWestRN@yahoo.com888-621-5557

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026