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The Effects of a Springtime Home Cleanse on Skin, Gut, Metabolic and Mental Health

The Effects of a Springtime Home Cleanse on Skin, Gut, Metabolic and Mental Health

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04869865
Enrollment
18
Registered
2021-05-03
Start date
2021-04-29
Completion date
2022-04-03
Last updated
2021-05-03

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

Conditions

Healthy

Keywords

mental health, skin health, gut health

Brief summary

This pilot study will evaluate the effects of a Springtime Home Cleanse on skin, gut, metabolic, and mental health. The study will also assess changes in overall quality of life. The results will be used to design a larger cleanse-based study in the future.

Detailed description

Short-term dietary cleanses and other popular detoxification methods are thought to eliminate accumulated toxins from the body and subsequently, promote health and well-being. Although previous studies have reported improvements in weight loss, blood pressure and insulin resistance with these practices, there is not enough scientific evidence to corroborate these claims. Therefore, the objective of this pilot study is to determine the effects of a short-term dietary cleanse on various parameters of skin, gut, metabolic and mental health and evaluate the aforementioned health claims.

Interventions

DIETARY_SUPPLEMENT9-day detoxification cleanse and 1 week of pre-cleanse transition

Subjects will participate in the full 9-day Springtime Home Cleanse, including the week prior to a pre-cleanse transition period. The cleanse includes a transition week, 9 days of a monodiet, internal oleation with ghee, external oleation, herbs, purgation, and an enema. During this time, subjects will also attend daily online meetings on Facebook Live throughout the cleanse and on AyurPrana's AyurLearn online portal to participate in guided mediation and yoga. Subjects will also use these platforms to access daily cleanse instructions and journaling topics.

Sponsors

AyurPrana LLC
CollaboratorUNKNOWN
Pearl Banyan, LLC
CollaboratorUNKNOWN
Integrative Skin Science and Research
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

All subjects will be given the intervention

Eligibility

Sex/Gender
ALL
Age
18 Years to 69 Years
Healthy volunteers
Yes

Inclusion criteria

* Males and females (ages 18-69) * Individuals must be able to read and comprehend study procedures and consent forms. * Individuals who have baseline metabolic, gut or stress dysfunction * Individuals must be able to minimize activity during the home cleanse for full participation and compliance. * Individuals must be willing to reduce caffeine, sugar, alcohol, dairy and carbohydrate rich foods throughout the study. * Individuals must be willing to have flash photo facial images taken with imaging systems.

Exclusion criteria

* Individuals with a known allergy to lime or lime juice, ginger or ginger pickle, turbinado sugar, rock salt, curcumin, coriander, fennel, cardamom, cinnamon, trikatu, yellow mung dal, kitchari spice, triphala, dashamula and guduchi powder, castor oil and chyavanprash. * Individuals who are lactose intolerant, or with a known allergy to ghee. * Individuals who are in the process of being vaccinated. * Individual who have a history of gastrointestinal inflammatory diseases or a history or diagnosis of immunologic or infectious disease (e.g. hepatitis, tuberculosis, HIV or AIDS, lupus, rheumatoid arthritis) or other similar systemic diseases in the opinion of the investigator. * Individuals who are recovering from a serious illness (requiring hospitalization), infection (requiring hospitalization), or surgery within one month of starting the study or unwilling to wait one month after their illness, infection, or surgery prior to starting the study. * Individuals who are recovering from a non-serious illness or infection who are recovered and unwilling to wait 2 weeks from their illness or infection. * Individuals who are in a concurrent intervention based clinical research study at this site or any other facility in the past two weeks. * Has a condition or is on a medication the investigator and/or designee believes could jeopardize the safety of the subject, interfere with the evaluation, or confound the interpretation of the study results. * Individuals who have had exposure to systemic antibiotics within the month prior or unwilling to wash out for a month. * Women who are pregnant or breastfeeding. * Individuals who are cognitively impaired. * Prisoners

Design outcomes

Primary

MeasureTime frameDescription
Microbiota diversity3 weeksEvaluation of gut microbiome diversity
Microbiome intestinal markers3 weeksZonulin, calprotectin, antibodies against LPS

Secondary

MeasureTime frameDescription
Serum low density lipoprotein (LDL) level3 weeksEvaluate serum LDL level via ZRT Laboratories Cardiometabolic Panel
Serum high density lipoprotein (HDL) level3 weeksEvaluate serum HDL level via ZRT Laboratories Cardiometabolic Panel
Serum very low density lipoprotein (VLDL) level3 weeksEvaluate serum VLDL level via ZRT Laboratories Cardiometabolic Panel
Salivary diurnal cortisol pattern3 weeksSalivary diurnal cortisol pattern via ZRT Laboratories Saliva Hormone Test
Serum hemoglobin A1c (HbA1c) levels3 weeksEvaluate serum HbA1c level via ZRT Laboratories Cardiometabolic Panel
Facial redness - image based3 weeksBTBP Clarity Mini 3D camera
Facial wrinkles - image based3 weeksBTBP Clarity Mini 3D camera
Serum high-sensitivity C-reactive protein (hsCRP) level3 weeksEvaluate serum hsCRP level via ZRT Laboratories Cardiometabolic Panel
Tongue changes - image based3 weeksEvaluate changes in tongue coating, discoloration, depressions, indentations, and cracking via iPad imaging
Quality of Life Survey Based Assessment3 weeksSelf assessment using World Health Organization (WHO) Quality of Life Questionnaire
Safety assessments for GI distress3 weeksSelf assessment using Digestive Questionnaire
Blood pressure3 weeks
Heart Rate3 weeks
Respiratory Rate3 weeks
Facial trans-epidermal water loss (TEWL)3 weeksVapometer, Delfin Technologies
Serum triglyceride (TG) level3 weeksEvaluate serum TG level via ZRT Laboratories Cardiometabolic Panel

Countries

United States

Contacts

Primary ContactRaja Sivamani, MD, MS, AP
raja.sivamani@integrativeskinresearch.com916-524-1216
Backup ContactMincy Chakkalakal, BS
mincy@integrativeskinresearch.com279-204-7338

Outcome results

None listed

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